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How Lactobacillus Protects Your Health
Reproduced from original article:
https://articles.mercola.com/sites/articles/archive/2023/12/14/lactobacillus-benefits.aspx
The original Mercola article may not remain on the original site, but I will endeavor to keep it on this site as long as I deem it to be appropriate.
Analysis by Dr. Joseph Mercola December 14, 2023
STORY AT-A-GLANCE
- Several studies have found that different strains of the Lactobacillacea family are diminished in people with anxiety and depression, and others have confirmed that different species of Lactobacillus can help prevent and/or treat these conditions
- Researchers at the University of Virginia School of Medicine discovered that Lactobacillus bacteria — found in many fermented foods, including yogurt — helps dampen stress responses and prevent depression and anxiety by modulating levels of an immune mediator called interferon gamma (IFNγ). In other words, these beneficial bacteria help “tune” your immune system
- Another recent paper describes how Lactobacillus inhibits the growth of gram-negative endotoxin-producing bacteria through a process known as competitive inhibition, and eliminating endotoxin is crucial for health
- Endotoxin is one of several factors that impairs mitochondrial function, promotes glycolysis and, ultimately, promotes cancer metabolism
- Lactobacilli also benefit your health by breaking down dietary fiber into beneficial short-chain fatty acids, breaking down phytonutrients such as polyphenols, which have anti-inflammatory and antioxidant benefits, promoting the growth of other beneficial gut microbes, and maintaining an appropriate pH level in your gut
I’ve often recommended traditionally fermented foods for their ability to “reseed” your gut with healthy bacteria. A healthy gut microbiome, in turn, can help ameliorate or reverse many chronic health conditions, as so much of your health is dependent on and can be traced back to your gut.
Even many mental health problems have in recent years been linked to gut health. Several studies1 have found that different strains of the Lactobacillacea2 family in particular are diminished in people with anxiety and depression. Others have confirmed that different species of Lactobacillus can help prevent and/or treat these conditions. So much so, Lactobacillus has been dubbed a “psychobiotic.”3
For instance, one 2011 study4 found that the probiotic Lactobacillus rhamnosus has a marked effect on GABA levels in certain brain regions and lowers the stress-induced hormone corticosterone, resulting in reduced anxiety- and depression-related behavior.
How Lactobacillus Regulates Your Mood
Most recently, researchers at the University of Virginia School of Medicine discovered5 that Lactobacillus bacteria — found in many fermented foods, including yogurt — helps dampen stress responses and prevent depression and anxiety by tuning your immune system. As reported by SciTech Daily:6
“The new research from UVA’s Alban Gaultier, Ph.D., and collaborators is notable because it pinpoints the role of Lactobacillus, separating it out from all the other microorganisms that naturally live in and on our bodies …
Our guts are naturally home to countless bacteria, fungi, and viruses … scientists have increasingly realized that these tiny organisms and their endless interactions are critical to our immune systems’ health, our mental health, and many other facets of our well-being.
Disruptions of the microbiota, whether from illness, poor diet, or other causes, are known to contribute to many diseases and even help cancer spread …
Early attempts to manipulate the gut flora with beneficial bacteria, called probiotics, have produced mixed results. A big part of the problem has been the sheer complexity of the microbiome … Gaultier and his team took an innovative approach to hone in on Lactobacilli …
Gaultier and his team decided to continue their depression research using … two strains of Lactobacillus [L. intestinalis and L. murinus] … Gaultier and his colleagues were able to explain exactly how Lactobacilli influence behavior, and how a lack of the bacteria can worsen depression and anxiety.”
According to these findings, one of the primary ways in which Lactobacillus helps prevent depression and regulate your body’s response to stress is by modulating levels of an immune mediator called interferon gamma (IFNγ). As explained by the authors:7
“… we found that the Lactobacillus species themselves, and not the disrupted microbial communities, are protective from environmental stressors. Further, we determine that Lactobacillacea are maintaining homeostatic IFNγ levels which are mediating these behavioral and circuit level responses …
By utilizing mice lacking Lactobacilli from birth, we found that Type 1 adaptive immunity is important as a primary mediating factor in stress resistance.
Building off a body of work showing that Lactobacillus is necessary for the maintenance of systemic IFNγ, we further demonstrate that both Lactobacilli and IFNγ are necessary for resilience to environmental stressors.”
Lactobacillus Prevents Endotoxin Production
Another recent paper,8 published in April 2022, describes how Lactobacillus inhibits the growth of gram-negative endotoxin-producing bacteria through a process known as competitive inhibition, and eliminating endotoxin is crucial for health in several respects.
Endotoxin, also known as lipopolysaccharide (LPS), is produced by gram-negative bacteria in your gut. As explained in several recent articles, endotoxin is one of several factors that destroys mitochondrial function, promotes glycolysis and, ultimately, cancer metabolism.
When complex carbs aren’t digested in your stomach, they travel down to the intestine where they feed these gram-negative bacteria, and as the bacteria grow, multiply and die, they release LPS, which can result in leaky gut, allergic reactions, organ dysfunction and even sepsis.
Endotoxin also catalyzes a series of metabolic reactions that convert tryptophan in your gut to serotonin. Most people think serotonin is good, but mostly, especially higher levels, it is not good for your health. You do not want high levels of serotonin because it’s an antimetabolite.
This means it suppresses your body’s ability to create energy in your mitochondria in the electron transport chain, so you become tired and fatigued, your metabolic rate slows and you gain weight.
To address this vicious cycle, you need to heal and seal your gut. Beneficial bacteria such as Bifidobacteria and Lactobacillus, and beneficial yeast like Saccharomyces boulardii, can all help rein in the endotoxin production through competitive inhibition.
Probiotics such as these also strengthen your intestinal barrier (the “seal” part of “heal and seal your gut”) by increasing mucus production, stimulating release of antimicrobial peptides and increasing tight junction integrity.9
Additionally, they tend to crowd out the gram negative bacteria by occupying space and territory and displacing them in the gut. In microbiology this is termed competitive inhibition and is one the reasons they help decrease endotoxin as there are simply less gram-negative bacteria.
At the same time, you also want to strictly limit your intake of refined sugar and most starches, as these types of carbs tend to feed the bacteria that produce endotoxin, especially if your microbiome is less than optimal. Alcohol is also best avoided, as it too can promote the growth of gram-negative bacteria and the accumulation of endotoxin.
As explained in a 2008 study,10 when gram-negative bacteria metabolize alcohol, they can also produce acetaldehyde, which increases intestinal permeability to endotoxin. In other words, the acetaldehyde facilitates the endotoxins’ entry into your blood circulation.
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Other Benefits of Lactobacilli
Lactobacilli also benefit your health by:
- Breaking down dietary fiber into beneficial short-chain fatty acids.
- Breaking down phytonutrients such as polyphenols, which have anti-inflammatory and antioxidant benefits.
- Promoting the growth of other beneficial gut microbes, including bacteria that produce butyrate, which is a fuel source for the cells in your gut lining and inhibits inflammation.11
- Maintaining an appropriate pH level in your gut by producing lactate and acetate from dietary fiber. And, by balancing the acidity in your gut, they encourage the proliferation of beneficial and harmless (commensal) bacteria while minimizing the harmful ones.
Specific strains have also been shown to be particularly beneficial for specific health conditions. For example:12
| L. acidophilus is recommended in the treatment of ulcerative colitis. |
| L. plantarum may ameliorate irritable bowel disease (IBD), irritable bowel syndrome (IBS), heart disease, cancer and gastrointestinal problems. It’s also been shown to decrease pathological hallmarks of Alzheimer’s, including amyloid plaques and tangles.13 |
| L. reuteri can be useful in the treatment of infant colic and leaky gut, and for the prevention of urogenital disease, dental caries and food sensitivities. |
| L. casei can help prevent antibiotic-associated diarrhea and clostridium difficile infections, and improve your body’s glucose response. |
| Preliminary animal research suggests L. paracasei might be able to prevent Type 2 diabetes by influencing genes involved in glucose metabolism.14 |
| L. rhamnosus has been shown to help women lose weight.15 |
| A probiotic milk product containing L. acidophilus, L. casei, Bifidobacterium bifidum and L. fermentum was shown to lower highly sensitive c-reactive protein levels (a marker of inflammation) by 18% after 12 weeks in elderly patients diagnosed with Alzheimer’s.16
Meanwhile, those who got a placebo saw a 45% increase in hs-CRP. The placebo group also continued to decline cognitively, while those who got the probiotics saw significant improvement in their mini-mental state examination (MMSE) scores. |
When it comes to mental health, three Lactobacillus species — L. casei, L. helveticus and L. rhamnosus — have been shown to reduce anxiety and depressive behavior. L. helveticus may also improve memory.17
How to Feed the Lactobacillus in Your Gut
The take-home here is that diversity matters, even within a single family of bacteria. The greater the diversity of your gut microbiome, the more likely you are to be able to maintain overall good health. There are three primary ways to increase the number of Lactobacilli and other beneficial bacteria in your gut:18
- Take a high-quality probiotic supplement that contains one or more strains.
- Consume fermented foods such as unpasteurized yogurt or kefir made from raw milk, sour cream, and fermented vegetables such as sauerkraut.
- Eat foods that promote proliferation of Lactobacilli, such as dietary fiber, Konjac flour, wheat bran, buckwheat, barley, apples, walnuts, artichoke and chokeberry.
- 1, 3 Brain, Behavior and Immunity January 2024; 115: 458-469, Introduction
- 2, 9, 11, 12, 14, 17, 18 Atlas Biomed Lactobacillus
- 4 Proc Natl Acad Sci U S A. 2011 Sep 20;108(38):16050-5
- 5, 7 Brain, Behavior and Immunity January 2024; 115: 458-469
- 6 SciTech Daily December 3, 2023
- 8 Frontiers in Immunology April 6, 2022; 13 DOI: 10.3389/fimmu.2022.840245, Competitive Resistance section
- 10 Alcohol August 2008; 42(5): 349-361
- 13 Journal of Clinical and Diagnostic Research 2017 Aug; 11(8): KC01–KC05
- 15 Wellnessresources.com January 4, 2014
- 16 Frontiers in Aging Neuroscience November 10, 2016 (PDF)
Health News in Review: A New C. difficile Treatment, New AMA Medical Education, and New Insights into Ribosome Oxidation and the Free Radical Theory of Aging
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Orthomolecular Medicine News Service, May 22, 2023
by Michael Passwater
OMNS (May 22, 2023) On April 26, 2023, the FDA approved Vowst for the prevention of recurrence of Clostridioides (formerly known as Clostridium) difficile infection (CDI). [1] There are approximately 500,000 cases of CDI each year in the United States, leading to 10,000 – 15,000 deaths per year. It is the most common hospital acquired infection. [2] C. diff is considered an opportunistic infection since it tends to only cause disease in people with weakened immune systems such as HIV/AIDS patients and transplant patients taking immunosuppressive medications, or people who have had their normal intestinal bacteria (“gut microbiome”) killed by antibiotics. Clindamycin, Fluoroquinolones, and Cephalosporins are the classes of antibiotics most commonly associated with C. diff and other forms of antibiotic associated diarrhea (AAD). The lack of host immune challenge or competition from healthy bacteria allows the invading C diff. bacteria to proliferate and cause illness. Interestingly, standard treatment for CDI is to administer additional antibiotics. Given their weakened, microbiome depleted state, it may not be surprising that people who have had CDI are more likely to suffer from the illness again.
The FDA granted the Vowst drug application “Priority,” “Breakthrough Therapy,” and “Orphan” status. The only alternative treatment recognized by the FDA for recurrent CDI is Rebyota, which the FDA approved Nov 30, 2022. [3] Both Rebyota and Vowst are fecal microbiota products, meaning they come from screened human donors of fecal matter (stool). Reboyta is administered rectally in a single dose. Vowst is administered orally as 4 pills per day for 3 days. Clinical trials with Reboyta showed a 71% success rate compared to a 58% success rate for a placebo, and Vowst showed an 87% success rate compared to a 60% success rate with a placebo. From both treatments, there is an unquantified risk of infectious disease transmission and food allergies due to the possibility of food particles and other fecal materials from the donor persisting in the finished product. One industry expert predicted the cost of a course of treatment with Vowst might be nearly $20,000. [4]
The concept of fortifying or replacing healthy bacteria in the intestines is not novel. Anecdotal, observational, and prospective clinical trials have suggested effectiveness and safety of a variety of probiotics and fermented foods for the prevention and treatment of AAD, including CDI. [5-23] In 2017, a Cochrane analysis of 31 clinical trials concluded there was moderate evidence of effectiveness and safety for probiotics. The analysis noted that more adverse events were seen in patients receiving placebos than patients receiving probiotics. These reviewers acknowledged the need for further studies, but felt the existing evidence was adequate to recommend advising hospitalized patients of the benefits and risks of probiotics. [24] In 2018, the Journal of the American Medical Association (JAMA) published a review of probiotic use with similar conclusions of efficacy and safety as the Cochrane analysis. [25] Maintaining adequate intestinal flora, especially during and after antibiotic treatment, is important for health. Healthy intestinal bacteria crowd out disease causing bacteria, produce vitamins, fatty acids, and other nutrients essential for a healthy body, and modulate the immune system.
Medical Education
The American Medical Association Education Hub (AMA Ed Hub) now offers a “Nutrition and Health” program with 48.5 continuing medical education units. Promotional material for the program states:
“Traditional medical models have discounted the importance of nutrition in health and in the prevention and management of a variety of health conditions, including cardiovascular disease, cancer, diabetes, and obesity. Recent overwhelming evidence has led to increased attention to nutrition as a core element of health, health equity and health care.” (AMA Ed Hub)
Overwhelming evidence, indeed! Although the program is not perfect, and has a distinct anti-supplement bias, it is a step in a healthy direction for American medicine. https://edhub.ama-assn.org/course/303
Those further along in their understanding of nutrition may prefer these educational resources:
International Society of Orthomolecular Medicine online learning: https://isom.ca/online-learning
The Riordon Clinic video library: https://riordanclinic.org/video-gallery
Free Radicals
In 1956, Denham Harman, MD, PhD, published the free radical theory of aging. [26] He suggested that highly reactive oxygen and nitrogen biomolecules generated by cellular respiration and stress caused many of the diseases of aging through destructive actions on cells and tissues. The term “free radical”, now more commonly called reactive oxygen and nitrogen species (RONS), refers to the unpaired electron in an oxygen or nitrogen molecule – an energy state that is not sustainable. [27] The molecule will steal an electron from the first thing it encounters, whether that is a nucleic acid, a protein, or a lipid, and cause a molecular chain reaction through the cell. “Antioxidants” are able to absorb or buffer the free radical by donating an electron to prevent or stop the chain reaction.
Dr. Harman suggested a low calorie, nutrient dense diet and supplementation with one or more inhibitors of oxidation could extend human life by 5 years or more. [28] His theory was met with ridicule and largely dismissed. Oxidative stress and, correspondingly, antioxidants, were not considered important to human health in that era. Even as supportive evidence steadily grew over the decades, criticism persisted. However, RONS have been generally accepted as important factors in many human biological processes. While not a complete explanation of all causes of aging and disease, Dr. Harman’s theory has helped advance our understanding of biochemistry. The evidence associating strong antioxidant capacity with wellness and longevity, and the number of diseases associated with oxidative stress continues to grow [29-35]. Dr. Harman never received a Nobel Prize, but he was nominated 6 times for the award.
Adding additional support to Dr. Harman’s concepts and the involvement of RONS and their neutralization in fundamental mechanisms preventing cellular damage, scientists at UF Scripps recently published insights into the mechanisms used by intracellular ribosomes to absorb free radical damage in a controlled fashion and replace the damaged proteins to restore the function of the ribosome. [36] Ribosomes are the factories that build all proteins. Ribosomes constitute roughly half of the mass of each cell in the human body. The ability of small segments of these critical organelles to “take a hit” to protect the rest of the ribosome is similar to the function of a bumper on an automobile. It is easier to repeatedly replace two proteins (Rps26, Rpl10) than to risk loss of an entire ribosome. Of note, the “bumper proteins” absorbing the free radical hits are rich in the sulfur containing amino acid cysteine, and zinc ions are critical for the bumper protein replacement process. The UF Scripps press release notes that the work could have implications for “cancer, the aging process, and growth and development.” If the damage control mechanism is overwhelmed by an excess of free radicals or if the cell lacks adequate repair materials, widespread ribosomal damage results, and therefore absent or altered protein production ensues which may lead to disease.
Summary
It is good to have choices. As the cost of health care in the United States continues to rise, while outcome measures such as lifespan continue to decline, a critical review of all available options to restore health and remain well is warranted. Informed choice allows wise selection of foods, vitamin and mineral supplements, activities, or prescriptions to address health concerns.
It is also encouraging to see the AMA recognize the key role of nutrition in human health – including serious diseases such as cardiovascular disease and cancer, and to provide increased access to nutrition education for physicians. Hopefully the new AMA “Nutrition and Health” program and similar ones will increase interest in the value of nutrition among healthcare providers and patients. As Hippocrates advised, “Let food be thy medicine and medicine be thy food.”
Continued careful research into the wondrous intricacies of human genetics and biochemistry increases our understanding of the connections between nutrients that serve as substrates, enzymes, and cofactors and the optimization of wellness. These mechanistic insights further inform choice.
“The doctor of the future will give no medication but will interest his patients in the care of the human frame, diet, and in the cause and prevention of disease” -Thomas A. Edison
References
1. FDA (2023) FDA Approves First Orally Administered Fecal Microbiota Product for the Recurrence of Clostridioides difficile Infection. https://www.fda.gov/news-events/press-announcements/fda-approves-first-orally-administered-fecal-microbiota-product-prevention-recurrence-clostridioides
2. CDC (2010) Clostridioides difficile Infection. https://www.cdc.gov/HAI/organisms/cdiff/Cdiff_infect.html
3. FDA (2022) FDA Approves First Fecal Microbiota Product. Nov 30, 2022. https://www.fda.gov/news-events/press-announcements/fda-approves-first-fecal-microbiota-product
4. Reuters (2023) US FDA approves Seres Therapeutics’ pill for deadly C. difficile infections. April 26, 2023. https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-approves-seres-therapeutics-pill-deadly-c-difficile-infections-2023-04-26
5. Kalakuntla AS, Nalakonda G, Nalakonda K, et al. (2019) Probiotics and Clostridium Difficile: A Review of Dysbiosis and the Rehabilitation of Gut Microbiota. Cureus. 11:e5063. https://pubmed.ncbi.nlm.nih.gov/31516774
6. Strohl M and Dyer D (2019) Diet and C. Difficile. Oncology Nutrition. https://www.oncologynutrition.org/erfc/eating-well-when-unwell/surgery/diet-and-c-difficile
7. Valdovinos MA, Montijo E, Abreu AT, et al. (2017) The Mexican consensus on probiotics in gastroenterology. Rev Gastoenterol Mex. 82:156-178. https://pubmed.ncbi.nlm.nih.gov/28104319
8. Cameron D, Hock QS, Kadim M, et al (2017) Probiotics for gastrointestinal disorders: proposed recommendations for children of the Asia-Pacific region. World J Gastroenterol. 23:7952-7964. https://pubmed.ncbi.nlm.nih.gov/29259371
9. Shen NT, Maw A, Tmanova LL, et al.(2017) Timely use of probiotics in hospitalized adults prevents Clostridium difficile infection: a systematic review with meta-regression analysis. Gastroenterology. 152:1889-1900. https://pubmed.ncbi.nlm.nih.gov/28192108
10. Sebastián Domingo JJ (2017) Review of the role of probiotics in gastrointestinal diseases in adults. Gastroenterol Hepatol. 40:417-429. https://pubmed.ncbi.nlm.nih.gov/28185664
11. Lewis PO, Lundberg TS, Tharp JL, Runnels CW. (2017) Implementation of global strategies to prevent hospital-onset Clostridium difficile infection: targeting proton pump inhibitors and probiotics. Ann Pharmacother. 51:848-854. https://pubmed.ncbi.nlm.nih.gov/28821215
12. Issa I, Moucari R. (2014) Probiotics for antibiotic-associated diarrhea: do we have a verdict? World J Gastroenterol. 20:17788-17795. https://pubmed.ncbi.nlm.nih.gov/25548477
13. Szajewska H, Canani RB, Guarino A, et al. (2016) Probiotics for the prevention of antibiotic-associated diarrhea in children. J Pediatr Gastroenterol Nutr. 62:495-506. https://pubmed.ncbi.nlm.nih.gov/26756877
14. Pace F, Pace M, Quartarone G. (2015) Probiotics in digestive diseases: focus on Lactobacillus GG. Minerva Gastroenterol Dietol. 61:273-292. https://pubmed.ncbi.nlm.nih.gov/26657927
15. Barker AK, Duster M, Valentine S, et al. (2017) A randomized controlled trial of probiotics for Clostridium difficile infection in adults (PICO). J Antimicrob Chemother. 72:3177-3180. https://pubmed.ncbi.nlm.nih.gov/28961980
16. Goldenberg JZ, Lytvyn L, Steurich J, et al. (2015) Probiotics For The Prevention Of Pediatric Antibiotic-Associated Diarrhea. Cochrane Database Syst Rev. 2015 Dec 22;(12):CD004827. https://pubmed.ncbi.nlm.nih.gov/26695080
17. McFarland LV (2007) Meta-Analysis Of Probiotics For The Prevention Of Traveler’s Diarrhea. Travel Med Infect Dis. 5:97-105. https://pubmed.ncbi.nlm.nih.gov/17298915
18. Basu S, Paul DK, Ganguly S, et al. (2009) Efficacy Of High-Dose Lactobacillus Rhamnosus GG In Controlling Acute Watery Diarrhea In Indian Children. J Clin Gastroenterol. 43:208-213. https://pubmed.ncbi.nlm.nih.gov/18813028
19. Guarino A, Guandalini S, Vecchio AL (2015) Probiotics For Prevention And Treatment Of Diarrhea. J Clin Gastroenterol. 49:S37-S45. https://pubmed.ncbi.nlm.nih.gov/26447963
20. Mu Q, Tavella VJ, Luo XM. (2018) Role Of Lactobacillus Reuteri In Human Health And Diseases. Front Microbiol. 9:757. https://pubmed.ncbi.nlm.nih.gov/29725324
21. Falagas ME, Betsi GI, Tokas T, Athanasiou S. (2006) Probiotics For Prevention Of Recurrent Urinary Tract Infections In Women. Drugs 66:1253-1261. https://pubmed.ncbi.nlm.nih.gov/16827601
22. Muresan AIP, Pop LL, Dumitrascu DL (2019) Lactobacillus Reuteri Versus Triple Therapy For The Eradication Of Helicobacter Pylori In Functional Dyspepsia. Med Pharm Rep. 92:352-355. https://pubmed.ncbi.nlm.nih.gov/31750434
23. Remes-Troche JM, Coss-Adame E, Valdovinos-Día MA, et al. (2020) Lactobacillus Acidophilus LB: A Useful Pharmabiotic For The Treatment Of Digestive Disorders. Therap Adv Gastroenterol. 13:1756284820971201. https://pubmed.ncbi.nlm.nih.gov/33281937
24. Goldenberg JZ, Yap C, Lytvyn L, et al. (2017) Probiotics for the prevention of Clostridium difficile-associated diarrhea in adults and children. Cochrane Database Syst Rev. 12:CD006095. https://pubmed.ncbi.nlm.nih.gov/29257353
25. Goldenberg JZ, Mertz D, Johnston BC. (2018) Probiotics to Prevent Clostridium difficile Infection in Patients Receiving Antibiotics. JAMA. 320:499-500. https://pubmed.ncbi.nlm.nih.gov/30027207
26. Harman D (1956) Aging: a theory based on free radical and radiation chemistry. J Gerontol. 11:298-300. https://doi.org/10.1093/geronj/11.3.298. https://pubmed.ncbi.nlm.nih.gov/13332224
27. Weidinger A, Kozlov AV (2015) Biological Activities of Reactive Oxygen and Nitrogen Species: Oxidative Stress versus Signal Transduction. Biomolecules 5:472-484. https://pubmed.ncbi.nlm.nih.gov/25884116
28. Harman D (1992) Free radical theory of aging: history. EXS. 62:1-10. https://pubmed.ncbi.nlm.nih.gov/1450577
29. Andersen HR, Jeune B, Nybo H, et al. (1998) Low Activity of Superoxide Dismutase and High Activity of Glutathione Reductase in Erythrocytes from Centenarians. Age Ageing 27:643-648. https://pubmed.ncbi.nlm.nih.gov/12675104
30. C.A. Lang, Mills BJ, Lang HL, et al. (2002) High Blood Glutathione Levels Accompany Excellent Physical and Mental Health in Women Ages 60 to 103 Years. J. Lab. Clin. Med. 140:380-381. https://pubmed.ncbi.nlm.nih.gov/12486409
31. Aykac K, Ozsurekci Y, Yayla BCC, et al. (2021) Oxidant and antioxidant balance in patients with COVID-19. Pediatr Pulmonol. 56:2803-2810. https://pubmed.ncbi.nlm.nih.gov/34265172
32. Nar R, Çalış AG. (2018) Assessment of dynamic thiol/disulfide homeostasis in patients with asthma. J Lab Med. 42:99-104. https://www.degruyter.com/document/doi/10.1515/labmed-2017-0144/html
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35. Taylor, E.W. (2009) The oxidative stress-induced niacin sink (OSINS) model for HIV pathogenesis. Toxicology 278: 124-130. https://pubmed.ncbi.nlm.nih.gov/19857540
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Is the Cause of Alzheimer’s Connected to Your Mouth?
Reproduced from original article:
https://articles.mercola.com/sites/articles/archive/2022/12/10/alzheimers-and-periodontal-disease.aspx
The original Mercola article may not remain on the original site, but I will endeavor to keep it on this site as long as I deem it to be appropriate.
Analysis by Dr. Joseph Mercola Fact Checked December 10, 2022<

STORY AT-A-GLANCE
- Periodontal disease may be a contributory factor in the development of Alzheimer’s disease
- In 2019, researchers identified Porphyromonas gingivalis (P. gingivalis), a pathogen involved in chronic periodontitis, in the brains of patients with Alzheimer’s disease
- Gingipains — toxic proteases from P. gingivalis — were also found in the brains of Alzheimer’s patients
- Levels of gingipains were associated with two markers of the disease, tau protein and another protein called ubiquitin
- In vivo and invitro studies also showed gingipains were neurotoxic and damaging to tau, which is needed for normal neuronal function
- The risk of Alzheimer’s disease and mild cognitive impairment in patients with periodontal disease is significantly higher than in those without periodontal disease, underscoring the importance of maintaining good oral health throughout your life
More than 6 million U.S. adults have Alzheimer’s disease. This number is expected to increase to nearly 13 million by 2050.1 Despite its growing prevalence, the causes of this devastating condition continue to be debated. There’s a growing consensus, however, that multiple factors play a role, from your gut health2 to your oral health.
Periodontitis, or gum disease, has been suggested as a potential risk factor for Alzheimer’s since at least 2015, when researchers with the University of Bristol noted “periodontal pathogens are possible contributors to neural inflammation and SLOAD [sporadic late onset Alzheimer’s disease].”3
Patients with Alzheimer’s disease often have poor oral health, which has commonly been attributed to declining self-care or neglect for oral health by caregivers. Now, however, it’s being recognized that periodontal disease may be a contributory factor in the disease’s development.4
Gum Disease Pathogen Found in the Brain
In 2019, researchers with the University of Louisville identified Porphyromonas gingivalis (P. gingivalis), a pathogen involved in chronic periodontitis, in the brains of patients with Alzheimer’s disease.5 Gingipains — toxic proteases from P. gingivalis — were also found in the brains of Alzheimer’s patients. Levels of gingipains were associated with two markers of the disease, tau protein and another protein called ubiquitin.6
Further, in mice, oral infection with P. gingivalis resulted in brain colonization of the pathogen, along with increased production of Aβ1-42, which is found in amyloid plaques. According to David Reynolds, Ph.D., chief scientific officer from Alzheimer’s Research UK:7
“Previously the P. gingivalis bacteria associated with gum disease has been found in the brains of people with Alzheimer’s but it remains unclear what role, if any, it plays in the development of the disease. In this well-conducted study, researchers were able to show that when mice were given P. gingivalis, the bacteria was found in the brain alongside higher levels of the hallmark Alzheimer’s protein, amyloid.”
In vivo and invitro studies also showed gingipains were neurotoxic and damaging to tau, which is needed for normal neuronal function. When the researchers designed small-molecule inhibitors to target gingipains, bacterial load was reduced, as was neuroinflammation. Production of Aβ1-42 was also blocked.
Together, the data suggest that gingipain inhibitors could target P. gingivalis in the brain and treat neurodegeneration from Alzheimer’s disease.8 P. gingivalis was also detected in the brains of people without Alzheimer’s disease, lending support for the theory that’s it’s involved in development of the condition and not simply a byproduct of it. According to the study:9
“Our identification of gingipain antigens in the brains of individuals with AD [Alzheimer’s disease] and also with AD pathology but no diagnosis of dementia argues that brain infection with P. gingivalis is not a result of poor dental care following the onset of dementia or a consequence of late-stage disease, but is an early event that can explain the pathology found in middle-aged individuals before cognitive decline.”
Periodontal Disease Linked to Increased Alzheimer’s Risk
A systematic review and meta-analysis that included 13 studies showed the risk of Alzheimer’s disease and mild cognitive impairment in patients with periodontal disease was significantly higher than in those without periodontal disease.10 This was especially true in people with severe periodontal disease.
A separate study, published in the Journal of Alzheimer’s disease, found that among people aged 65 and older, Alzheimer’s disease incidence and mortality were consistently associated with probing pocket depth, a measure of periodontal health, as well as Prevotella melaninogenica (P. melaninogenica) and Campylobacter rectus (C. rectus), bacterial markers of periodontitis.11
According to the researchers, “This study provides evidence for an association between periodontal pathogens and AD, which was stronger for older adults.”12 What’s more, the risk of cognitive decline in older men increases the more teeth are lost, while periodontal disease and caries, both of which contribute to tooth loss, are also linked to cognitive decline.13
How Gum Disease Leads to Alzheimer’s
Periodontal disease likely contributes to Alzheimer’s by increasing pro-inflammatory mediators, including C-reactive protein (CRP), IL-6, IL-1β, and TNF-α.14 According to researchers with the University of California School of Dentistry, three primary mechanisms have been identified for how periodontal disease may lead to Alzheimer’s:15
- Increased peripheral pro-inflammatory cytokines that systemically affect the brain via neural, humoral and cellular mechanisms
- Ectopic migration of periodontal bacteria and related molecules directly to the brain via blood and/or cranial nerves
- Leptomeninges (tissue covering the brain and spinal cord) that may act as a mode of communication between periodontal pathogens and microglia in the brain
In an editorial published in Expert Review of Anti-infective Therapy, it’s further explained:16
“A plethora of studies firmly place P.gingivalis … in the red complex as a risk factor for AD. This is because P.gingivalis is adept at modifying the peripheral and intracerebral immune responses.
Furthermore, this bacterium has a range of enzymes including cathepsin B and gingipains that are, respectively, shown to interact with the amyloid precursor protein (APP) and neuronal tau resulting in the formation of amyloid-beta (Aβ) and neurofibrillary tangles (NFTs), which are the cardinal hallmarks of AD.
Prospective, retrospective population-based, and nested control studies have shown that the risk of developing the sporadic form of AD doubles when periodontal disease persists for about 10 years.”
Since deposits of amyloid beta in the brain may start one to two decades before cognitive decline and diagnosis of Alzheimer’s disease, and periodontal disease may also be persistent for about 10 years to initiate Alzheimer’s, positive oral health early on may help prevent the disease.17
This is important not just for older adults, but also middle-aged and younger adults, who may be able to protect their brain health by maintaining good oral health. Even in young, otherwise healthy, adults, episodic memory and learning rate are improved among those without good oral health compared to those with aggressive periodontal disease18 — suggesting damage to brain health may start early on.
Proper oral hygiene, including regular brushing, flossing and tongue scraping, and getting regular cleanings with a mercury-free biological dentist, will go a long way toward keeping your teeth and gums healthy. A lifestyle that includes a diet based on fresh, whole foods is also essential to a naturally clean mouth and good oral health.
What Else Contributes to Alzheimer’s?
With a complex condition like Alzheimer’s, oral health is only one contributing factor. Gut health is another. A team of Swiss and Italian researchers found a connection between imbalanced gut microbiota and the development of amyloid plaques in the brain.19
The researchers used PET imaging to measure amyloid deposition in their brains, then measured markers of inflammation and proteins produced by intestinal bacteria, such as lipopolysaccharides (LPSs) and short-chain fatty acids (SCFAs), in their blood.
The study revealed that high blood levels of LPSs and SCFAs acetate and valerate were associated with large amyloid deposits in the brain. Other SCFAs, namely butyrate, appeared to have a protective effect; high levels of butyrate were associated with less amyloid.
“Our results are indisputable: certain bacterial products of the intestinal microbiota are correlated with the quantity of amyloid plaques in the brain,” explains Moira Marizzoni, a study author with the Fatebenefratelli Center in Brescia, Italy.20 It’s not surprising, then, that probiotics have been shown to be protective.
A 2016 study of 60 Alzheimer’s patients found those who drank milk containing probiotics experienced significant improvements in cognitive function.21 Probiotics, by the way, are also useful for managing periodontal disease.22
Electromagnetic exposures from wireless technologies are another crucial component that need to be addressed. This type of radiation activates the voltage-gated calcium channels (VGCCs) in your cells, and the greatest density of VGCCs are in your brain, the pacemaker of your heart and male testes.
A 2022 study that summarized 18 different findings found they “collectively provide powerful evidence for EMF causation of AD.” Further, “The author is concerned that smarter, more highly pulsed ‘smart’ wireless communication may cause widespread very, very early onset AD in human populations.”23
It is my belief that excessive microwave exposure and mitochondrial dysfunction are among the most significant factors contributing to Alzheimer’s, along with exposure to the herbicide glyphosate, which also has negative neurological effects.24
Tips for Alzheimer’s Prevention
Overall, nourishing your brain health is best done with a comprehensively healthy lifestyle, including healthy diet. Not only does what you eat affect your oral and gut health, but it also impacts cholesterol, and cholesterol also plays an important role in the formation of memories and is vital for healthy neurological function.
As noted by senior research scientist Stephanie Seneff, Ph.D., insufficient fat and cholesterol in your brain play a crucial role in the Alzheimer’s disease process, detailed in her 2009 paper “APOE-4: The Clue to Why Low Fat Diet and Statins May Cause Alzheimer’s.”25
Time-restricted eating is another important strategy, as is reducing your intake of polyunsaturated fatty acids, also called PUFAs, found in vegetable oils, edible oils, seed oils, trans fat and plant oils. For a more targeted approach, natural options are available.
Animal and laboratory studies demonstrate that the spice saffron is neuroprotective, for instance. Data also show it’s as effective as the drug memantine to treat moderate to severe Alzheimer’s disease.26 One of the most comprehensive assessments of Alzheimer’s risk is Dr. Dale Bredesen’s ReCODE protocol, which evaluates 150 factors, including biochemistry, genetics and historical imaging, known to contribute to Alzheimer’s disease.
In his book, “The End of Alzheimer’s: The First Program to Prevent and Reverse Cognitive Decline,”27 which describes the complete protocol, you will also find a list of suggested screening tests and the recommended ranges for each test, along with some of Bredesen’s treatment suggestions. By leveraging 36 healthy lifestyle parameters, Bredesen was able to reverse Alzheimer’s in 9 out of 10 patients.
This included the use of exercise, ketogenic diet, optimizing vitamin D and other hormones, increasing sleep, meditation, detoxification and eliminating gluten and processed food. For more details, you can download Bredesen’s full-text case paper online, which details the full program.28
- 1 Alzheimer’s Association, Facts and Figures, Quick Facts
- 2, 20 Science Daily November 13, 2020
- 3 Br Dent J. 2015 Jan;218(1):29-34. doi: 10.1038/sj.bdj.2014.1137
- 4, 14, 15, 18 Front Cell Infect Microbiol. 2021; 11: 766944., Alzheimer’s Disease and Cognitive Dysfunction
- 5, 8 Science Advances January 23, 2019
- 6 Science Alert November 22, 2022
- 7 Alzheimer’s Research UK January 23, 2019
- 9 Science Advances January 23, 2019, Discussion
- 10 Psychogeriatrics. 2021 Sep;21(5):813-825. doi: 10.1111/psyg.12743. Epub 2021 Jul 11
- 11, 12 J Alzheimers Dis. 2020;75(1):157-172. doi: 10.3233/JAD-200064
- 13 Journal of the American Geriatrics Society April 1, 2010
- 16 Expert Rev Anti Infect Ther. 2020 Nov;18(11):1063-1066. doi: 10.1080/14787210.2020.1792292. Epub 2020 Jul 14., Introduction
- 17 Expert Rev Anti Infect Ther. 2020 Nov;18(11):1063-1066. doi: 10.1080/14787210.2020.1792292. Epub 2020 Jul 14
- 19 J Alzheimers Dis. 2020;78(2):683-697. doi: 10.3233/JAD-200306
- 21 Frontiers in Aging Neuroscience November 10, 2016
- 22 J Dent. 2016 May;48:16-25. doi: 10.1016/j.jdent.2016.03.002. Epub 2016 Mar 8
- 23 Curr Alzheimer Res. 2022;19(2):119-132. doi: 10.2174/1567205019666220202114510
- 24 Neurotoxicology. 2019 Dec;75:1-8. doi: 10.1016/j.neuro.2019.08.006. Epub 2019 Aug 20
- 25 MIT.edu APOE-4: The Clue to Why Low Fat Diet and Statins May Cause Alzheimer’s by Stephanie Seneff
- 26 Human Psychopharmacology, 2014;29(4)
- 27 Amazon.com, The End of Alzheimer’s: The First Program to Prevent and Reverse Cognitive Decline, by Dr. Dale Bredesen
- 28 Aging September 27, 2014; 6(9): 707-717
How Gut Bacteria Influence Your Metabolism
Reproduced from original article:
https://articles.mercola.com/sites/articles/archive/2022/08/06/gut-bacteria-and-metabolism.aspx
The original Mercola article may not remain on the original site, but I will endeavor to keep it on this site as long as I deem it to be appropriate, and will not be bullied into removing it.
Analysis by Dr. Joseph Mercola Fact Checked August 06, 2022

STORY AT-A-GLANCE
- Any given individual will have around 160 different species of bacteria colonizing their gut. This individual combination is known as your gut microbiome, and can have a tremendous influence on health and well-being
- Obesity is associated with as much as a 40% decrease in bacterial diversity. Improving diversity through probiotic supplementation can help resolve metabolic defects, resulting in fat loss
- Research has demonstrated that probiotics — beneficial bacteria found in fermented and cultured foods such as yogurt — have a measurable effect on several metabolic pathways
- A link has also been found between bowel movements and obesity; 8.5% of obese and 11.5% of severely obese individuals reported chronic diarrhea, compared to 4.5% of those with normal weight
- One hypothesis is that chronic low-grade inflammation is at play. Not only is chronic inflammation a factor in obesity, but it can also contribute to diarrhea
This article was previously published September 30, 2019, and has been updated with new information.
Before we review the evidence that your gut flora plays a role in regulating your metabolism and likely is a factor in the development of obesity, please understand that there is beyond overwhelming evidence that excess seed oils and an increase in linoleic acid is likely the primary factor contributing to the obesity epidemic as discussed in my interview with Tucker Goodrich.
Hippocrates once said that “all disease begins in the gut,”1 and the more we learn, the more accurate that statement proves to be. As noted in a 2018 paper:2
“While often-quoted figures suggest that the microbes that live in and on the human body outnumber human cells by 10:1, a more recent estimate suggests that we are essentially one part human to one part microbe in terms of cell number.3
These commensal microorganisms have a vital role in human health. They break down otherwise indigestible dietary fibers and other components of food, produce vitamins, promote the development and maturation of the immune system, and prevent pathogenic bacterial species from colonizing the gut.”
According to evidence cited in this paper, of the 1,000 or so gut bacteria we know of, any given individual will have around 160 different species of bacteria colonizing their gut. This individual combination is known as your gut microbiome, and can have a tremendous influence on health and well-being.
The diversity of your gut microbiome begins to be established when you are an infant, and is affected by genetics, whether you are breast- or bottle-fed, and your immediate environment. Later in life your microbiome is significantly affected by your food choices.4
Diets high in sugar and processed foods may reduce the diversity and your overall health, while diets high in whole foods high in fiber tend to have a beneficial impact. For example, a number of studies have found obese individuals tend to have a less diverse gut microbiome,5 in addition to having greater numbers of certain harmful bacteria and fewer beneficial ones.
Studies have shown obesity is associated with as much as a 40% decrease in diversity,6 and that improving that diversity through probiotic supplementation can help resolve metabolic defects, resulting in fat loss.7
Obesity Associated With Frequent Diarrhea
There’s also a link between abnormal bowel movements and obesity, according to research8 published in September 2019. As reported by Medical Xpress:9
“In the most comprehensive analysis of the relationship between Body Mass Index (BMI) and bowel habits to date, published today in Alimentary Pharmacology & Therapeutics, a team of physician-researchers at Beth Israel Deaconess Medical Center (BIDMC) found a strong association between obesity and chronic diarrhea independent of an individual’s dietary, lifestyle, psychological factors or medical conditions …
‘While several previous studies have pointed to an association between obesity and bowel habits, all lacked data on whether dietary or other factors drive the connection,’ said corresponding author Sarah Ballou, Ph.D., a health psychologist in the Division of Gastroenterology, Hepatology, and Nutrition at BIDMC.
‘Our research confirms a positive association between obesity and chronic diarrhea and reveals for the first time that this relationship is not driven by confounding factors such as diet or physical activity level.'”
Looking at data from the 2009-2010 National Health and Nutrition Examination Survey, the researchers found 8.5% of obese and 11.5% of severely obese individuals reported chronic diarrhea, compared to 4.5% of those with normal weight. “Stepwise regression revealed that severe obesity was independently associated with increased risk of diarrhea,” the authors say.
Unfortunately, this study cannot shed light on why this is happening. One hypothesis is that chronic low-grade inflammation is at play. Not only is chronic inflammation a factor in obesity,10 but it can also contribute to diarrhea.
Systemic inflammation is also believed to be one of the leading triggers for other serious diseases, including neurological degeneration,11 Type 2 diabetes12 and cardiovascular disease13 — all of which, by the way, are also associated with obesity.
Committing to making changes to your gut microbiome can do far more than improve your bowel habits. Your gut health is important to most aspects of your health, including reducing your risk for cancer, metabolic syndrome and depression.
Probiotics Shown to Alter Metabolism
Improving your microbiome can be as simple as increasing your intake of fermented foods or taking a quality probiotic supplement. Previous research has demonstrated that probiotics — beneficial bacteria found in fermented and cultured foods such as yogurt — have a measurable effect on your metabolism.
One such study,14 published in 2008, found the bacterial strains Lactobacillus paracasei and Lactobacillus rhamnosus affected a number of different metabolic pathways, including the metabolism of:
- Hepatic lipids
- Amino-acids
- Methylamines
- Short-chain fatty acids (SCFAs)
As reported by Science Daily:15
“Adding ‘friendly’ bacteria changed the makeup of the bugs in the gut, not only because this increased the number of such bacteria, but also because the ‘friendly’ bacteria worked with other bacteria in the gut, amplifying their effects.
One of the many biochemical changes observed by the researchers was a change in how mice treated with probiotics metabolized bile acids. These acids are made by the liver and their primary function is to emulsify fats in the upper gut. If probiotics can influence the way in which bile acids are metabolized, this means they could change how much fat the body is able to absorb.”
While some claim taking probiotic supplements or eating fermented foods won’t have a significant impact on your microbiome, this particular study found otherwise. As noted by corresponding author Jeremy Nicholson with the department of biomolecular medicine at Imperial College:16
“Some argue that probiotics can’t change your gut microflora — whilst there are at least a billion bacteria in a pot of yoghurt, there are a hundred trillion in the gut, so you’re just whistling in the wind.
Our study shows that probiotics can have an effect and they interact with the local ecology and talk to other bacteria. We’re still trying to understand what the changes they bring about might mean, in terms of overall health, but we have established that introducing ‘friendly’ bacteria can change the dynamics of the whole population of microbes in the gut.”
Can Probiotics Effectively Aid in Fighting Obesity?
So, can probiotics actually have a beneficial impact on obesity? A number of studies suggest the answer is yes. Among them is a 2013 animal study,17 which found the probiotics Lactobacillus gasseri BNR17, found in human breast milk, act as an obesity inhibitor and antidiabetic.
According to the authors, “The administration of L. gasseri BNR17 significantly reduced the body weight and white adipose tissue weight regardless of the dose administered.” Such findings jibe well with studies18 showing breastfed babies have a significantly lower risk of childhood obesity.
In another study19 published that same year, obese participants with a fasting blood sugar level above 100 mg/dL were given either BNR17 or a placebo for 12 weeks. At the end of the study, the treatment group had shed more body fat than the controls. As reported by the authors, “Despite there being no change in behavior or diet, administration of only the supplement of BNR17 reduced weight and waist and hip circumference.”
Lactobacillus gasseri has also been shown to ease symptoms of irritable bowel syndrome and ulcerative colitis,20 thanks to its anti-inflammatory effects. L. gasseri is also one of four bacterial strains shown to help eradicate Helicobacter pylori,21 a primary cause of stomach ulcers.
A more recent review,22 published in the journal Nutrients in February 2019, sought to “present evidence … demonstrating the effects of various probiotic strains and their potential efficacy in improving obesity and associated metabolic dysfunctions.” As noted in this paper:23
“A large body of evidence has described several possible mechanisms by which the gut microbiota can contribute to, and/or influence, obesity.
Although so much is still unknown and debatable, thus far there is a general consensus that the gut microbiota is implicated in obesity through dietary carbohydrate fermentation, lipogenesis, excess energy storage, and several other pathways including a vast array of metabolites, hormones and neurotransmitters, some of which are known to control food intake and the regulation of energy balance.”
How Gut Bacteria Can Influence Your Fat Stores
Three main phyla or groups of gut microbes make up the human microbiome and serve diverse structural, protective and metabolic functions:24
- Bacteroidetes — Porphyromonas, Prevotella and Bacteroides
- Firmicutes — Ruminococcus, Clostridium, Lactobacillus and Eubacteria
- Actinobacteria — Bifidobacteria (the most prevalent type)
As explained in the 2019 Nutrients review,25 in your gut, these bacteria protect your health by “displacing harmful bacteria, competing with pathogens for nutrients and producing antimicrobial factors.”
Structural functions provided by them include “developing the immune system, inducing immunoglobulin A (IgA), and reinforcing the mucosal barrier,” while metabolic functions “benefit the host by synthesizing vitamin K, folate and biotin” and play a role in the absorption of minerals such as magnesium, calcium and iron.
Importantly, gut bacteria also help break down the foods you eat and ferment digestive-resistant starches, turning them into beneficial SCFAs, which help modulate your immune response and inflammation.26 As explained in the 2019 Nutrients review:27
“Degradation of dietary polysaccharides and fiber by Bacteroides and Firmicutes in the gut results in the production of SCFAs, such as propionate, acetate, and butyrate.
Propionate is an important energy source for the host via de novo synthesis of lipids and glucose in the liver. Acetate is used in peripheral tissues as a substrate for cholesterol synthesis while butyrate represents a rich energy source for the epithelial cells that line the colon.
Furthermore, microbiota is involved in the control of energy balance, food intake, and satiety via gut peptide signaling, through hormonal effects in the blood or by modulating the nervous system directly. The appropriate balance of these regulatory peptides may be disrupted if the microbiota composition is altered …
SCFAs … also serve as signaling molecules that can activate G-protein coupled receptors (GPRs), including GPR43 (also known as free fatty acid receptor 2) in adipose and intestinal tissues.
In adipose tissue, SCFAs bind to GPR43, thus promoting adipogenesis and increasing energy expenditure. In intestinal tissue, SCFAs bind to GPR43 leading to secretion of anorexigenic peptides … resulting in improved glucose tolerance and increased energy utilization.”
Since SCFAs play such an important role in fat accumulation, the two phyla that produce SCFAs, Firmicutes and Bacteroidetes, may be used as markers for obesity. As noted in the 2019 review, obese individuals tend to have higher proportions of Firmicutes and Lactobacillus and lower proportion of Bacteroidetes and Bifidobacterium compared to normal weight individuals.28
Studies have also linked specific strains to specific health problems. For example, high levels of Bacteroides vulgatus (which is abundant in the human gut) appear strongly associated with inflammation, insulin resistance and altered metabolism.
Low levels of certain bacteria in the Firmicutes phylum, including Blautia and Faecalibacterium, have been linked to the accumulation of trunk-fat specifically.29
How Probiotics Can Benefit Your Health and Weight
The 2019 Nutrients review also details the mechanisms by which supplementation with probiotics can improve your health and weight. Key areas of influence include:30
- Enhancing the integrity of your intestinal epithelial barrier
- Enhancing the adhesion of bacteria to your intestinal mucosa, thereby facilitating colonization
- Producing antimicrobial and other health promoting substances
- Inhibiting pathogenic microbes by competitive exclusion
- Modulating your immune system
While individual strains of bacteria have been linked to specific health effects such as reductions in trunk fat or lowered inflammation, several studies have demonstrated that multi-strain probiotics may be more beneficial than single-strain ones, as they tend to create synergistic effects.31
An Easy, Inexpensive Way to Improve Your Gut Microbiome
While probiotic supplements are widely available, few can compete with traditionally fermented foods, in terms of the diversity and sheer number of probiotics.
Fermented foods are also your least expensive alternative, as you can easily make them at home. Using a starter culture will speed the process and ensure you’ll end up with a consistent, high-quality product.
Remember, your diet is one of the easiest, fastest and most effective ways to improve and optimize your microbiome, so the good news is you have a great degree of control over your health destiny.
- 1, 2 Brain March 2018; 141(3): e20
- 3 PLOS Biology August 2016;14(8):e100253
- 4 Cell Host and Microbe December 2016; 21(1): 84-96
- 5 Nature 2013 Aug 29;500(7464):541-6
- 6 Nature 2013 Aug 29;500(7464):585-8
- 7, 23 Nutrients 2019 Feb; 11(2): 258, Introduction
- 8 Alimentary Pharmacology & Therapeutics September 18, 2019 DOI: 10.111/apt.15500
- 9 Medical Xpress September 18, 2019
- 10, 12 Diabetes Research and Clinical Practice, 2014; 105(2):141-150
- 11 Frontiers in Cellular Neuroscience, 2015; 9:28
- 13 Clinical Medicine Insights, Cardiology, 2015; 7(8):13-21
- 14 Mol. Syst. Biol. January 15, 2008; 4: 157
- 15, 16 Science Daily January 16, 2008
- 17 PLOS ONE 2013; 8(1): e54617
- 18 BMC Public Health 2014; 14: 1267
- 19 Korean Journal of Family Medicine 2013 Mar; 34(2): 80–8
- 20 Ulcers 2011, Article ID 841651
- 21 PLOS One November 3, 2014 DOI: 10.1371/journal.pone.0111030
- 22 Nutrients 2019 Feb; 11(2): 258
- 24, 25 Nutrients 2019 Feb; 11(2): 258, 2. Gut Microbiota Composition and Function
- 26 Science Direct, Modulation of Inflammatory and Immune Responses by Short-Chain Fatty Acids
- 27 Nutrients 2019 Feb; 11(2): 258, 3. Gut Microbiota and Obesity
- 28, 29 Nutrients 2019 Feb; 11(2): 258, 4. Gut Microbiota Strains and Obesity
- 30 Nutrients 2019 Feb; 11(2): 258, 5. Modulation of Gut Microbiota by Probiotics
- 31 Nutrients 2019 Feb; 11(2): 258, 7.3 Multi-Strain Probiotics
Top 9 Nutrients for Better Brain Health
Reproduced from original article:
https://articles.mercola.com/sites/articles/archive/2022/07/26/nutrients-for-brain-health.aspx
The original Mercola article may not remain on the original site, but I will endeavor to keep it on this site as long as I deem it to be appropriate, and will not be bullied into removing it.
Analysis by Dr. Joseph Mercola Fact Checked July 26, 2022

STORY AT-A-GLANCE
- Nine nutrients that are vital for brain health and cognition are the marine-based omega-3 fats DHA and EPA, choline, phosphatidylserine, acetyl-L-carnitine, vitamins D and B12, MCT oil and probiotics
- By using a lysophospholipid form of EPA (LPC-EPA), researchers were able to increase the EPA level in the brain of mice 100-fold. LPC-EPA also doubled the DHA level in the brain, whereas free EPA had no effect on DHA levels
- Choline helps protect against Alzheimer’s by reducing your homocysteine level, an amino acid associated with neurodegeneration and formation of amyloid plaques, and inhibiting microglia activation, which inhibits brain inflammation
- Supplementing with 400 mg of phosphatidylserine increased the speed of calculations done in short-term memory by 20% in one study. In another, 300 mg/day improved cognitive function of geriatric patients
- Low vitamin D is associated with poorer brain function, and increasing levels may help keep older adults mentally fit. Vitamin D has also been shown to improve a number of brain disorders, including dementia and Alzheimer’s disease
This article was previously published January 24, 2019, and has been updated with new information.
Like autism among children, Alzheimer’s among seniors has reached epidemic proportions, with no slowdown in sight. On the contrary, evidence suggests the trend is worsening. In 2022, Alzheimer’s affects about 6.5 million Americans age 65 and older; of this number, 73% are over age 75. Alzheimer’s is the fifth leading cause of death in the U.S.1 The World Health Organization predicts that by 2050, 139 million adults worldwide will be living with dementia.2
It’s important to realize that dementia is a lifestyle-predicated disease, and there are many strategies that will help prevent this kind of neurodegeneration. In essence, anything that will help optimize your mitochondria will also help prevent Alzheimer’s.
Here, the focus is on specific nutrients shown to play an important role in brain health and cognition, starting with marine-based omega-3, which contains two long-chained fatty acids that are vital for brain health: docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA).
1. Marine-Based Omega-3 Fat: DHA
The influence of marine-based omega-3 fats on physical and mental health has been the subject of intense research for decades, and there’s compelling evidence they can help ameliorate a variety of psychiatric illnesses and degenerative brain disorders, including Alzheimer’s.
In my book, “Superfuel,” cowritten with James DiNicolantonio, Pharm. D., we explain how DHA is an essential structural component of your brain, and is found in high levels in your neurons, the cells of your central nervous system. When your omega-3 intake is inadequate, your nerve cells become stiff and more prone to inflammation as the missing omega-3 fats are substituted with omega-6 instead.

Once your nerve cells become rigid and inflamed, proper neurotransmission from cell to cell and within cells become compromised. Low DHA levels have been linked to memory loss and Alzheimer’s disease, and some studies suggest degenerative brain diseases may potentially be reversible with sufficient DHA.
For example, in one study,3 elderly volunteers suffering from memory deficits saw significant improvement after taking 900 milligrams (mg) of DHA per day for 24 weeks, compared to controls. Another study4 found significant improvement in verbal fluency scores after taking 800 mg of DHA per day for four months, compared with placebo. Furthermore, memory and rate of learning were significantly improved when DHA was combined with 12 mg of lutein per day.
I never previously realized this but DHA also stimulates one of the most important transcription factors that regulates cellular oxidation and reduction, and aids in detoxification, the Nrf2 pathway.5 Additionally, it also increases heme oxygenase 16 (a protein produced in response to oxidative stress) and upregulates antioxidant enzymes — all of which are important for brain health.
In addition, DHA is a precursor for the signaling molecule protectin, which is synthesized in response to oxidative stress. (When found in your central nervous system it’s referred to as neuroprotectin, or NPD1.) As explained in a 2011 paper in the journal Nutrients:7
“NPD1 induces nerve regeneration, reduce leukocyte infiltration and maintains homeostasis through ageing by reducing pro-apoptotic and pro-inflammatory signaling. NPDI is induced by oxidative stress and protects retinal and neuronal cells from oxidative stress-induced apoptosis.
Many mechanisms have been implicated, including suppression of the IL-1β induced stimulation of COX. The discovery of NPD1 offers new therapeutic opportunities for a range of neurodegenerative conditions, such as Alzheimer’s disease. It also provides an exciting potential for DHA in helping to delay or minimize the ‘normal’ cognitive decline during ageing.”
2. Marine-Based Omega-3 Fat: EPA
EPA, meanwhile, appears to be particularly beneficial in the treatment of depression,8 as it helps lower levels of tumor necrosis factor alpha, interleukin 1 beta and prostaglandin E2 — three immune chemicals that tend to be elevated in those with depression.
A stumbling block has been to get sufficiently large amounts into your brain. To raise your brain level of EPA, you’d need to consume impractically large amounts of fish oil, for example. One theory is that degradation by pancreatic enzymes renders the EPA incapable of passing the blood-brain-barrier.9
However, recent research10 has discovered something really interesting. By using a lysophospholipid form of EPA (LPC-EPA), they were able to increase the EPA level in the brain of mice 100-fold. Even more remarkable, LPC-EPA also doubled the DHA level in the brain, whereas free EPA had no effect on DHA levels. The authors further noted that:
“Only LPC-EPA increased EPA and DHA in retina, and expression of BDNF, CREB and 5-HT1A receptor in the brain. These novel results show that brain EPA can be increased through diet. Because LPC-EPA increased both EPA and DHA in the brain, it may help treat depression as well as neuroinflammatory diseases, such as Alzheimer’s disease.”
Papasani Subbaiah, professor of medicine and biochemistry and molecular genetics in the UIC College of Medicine and corresponding author, told MedicalXpress:11
“It seems that there is a transporter at the blood-brain barrier that EPA must pass through in order to get into the brain, but EPA in fish oil can’t get through, whereas LPC-EPA can. You don’t have to consume all that much LPC- EPA to have significant increases of EPA show up in the brain, so this could be a way to do rigorous studies on the effects of EPA in humans.”
The Importance of Phospholipid-Bound Omega-3
There are a number of drawbacks to fish oil, and the lack of phospholipids is one of them. DHA and EPA are water insoluble and therefore cannot be transported in their free form in your blood. They must be packaged into lipoprotein vehicles such as phospholipids. This is primarily why the bioavailability of krill oil is so much higher than fish oil, because in fish oil, the DHA and EPA are bound to triglycerides.
When you consume fish oil, your liver has to attach it to phosphatidylcholine in order for it to be efficiently utilized by your body and brain. Phospholipids are also one of the principal compounds in high-density lipoproteins (HDL), which you want more of, and by allowing your cells to maintain structural integrity, phospholipids help your cells function optimally.
Importantly, your brain cannot readily absorb DHA unless it’s bound to phosphatidylcholine, and while krill oil contains phosphatidylcholine naturally, fish oil does not. As the name implies, phosphatidylcholine is composed partly of choline, the precursor for the vital neurotransmitter acetylcholine, which sends nerve signals to your brain, and choline itself is crucial for brain development, learning and memory, as you’ll see in the next section.
Recent research12 by Rhonda Patrick, Ph.D., also highlights the value of DHA bound to phospholipids, showing this form may actually reduce the risk of Alzheimer’s disease in those with the apolipoprotein E4 (APOE4) gene, which lowers the typical age of onset of this degenerative brain disorder.
Two hallmarks of Alzheimer’s are amyloid beta plaques and tau tangles, both of which impair normal brain functioning. Alzheimer’s patients also have reduced glucose transport into their brains, and this is one of the reasons why plaque and tangles form and accumulate in the first place. According to Patrick,13 DHA encourages your brain’s uptake of glucose by regulating the structure and function of glucose transporters, proteins located at your blood-brain barrier.
While eating DHA-rich fish has been shown to slow the progression of Alzheimer’s in APOE4 carriers, taking fish oil has not demonstrated the same efficacy. According to Patrick, this variation in response appears to be related to the different ways in which the two forms of DHA are metabolized and ultimately transported into your brain.
When the triglyceride form of DHA is metabolized, most of it turns into nonesterified DHA, while the phospholipid form is metabolized primarily into DHA-lysophosphatidylcholine (DHA-lysoPC). While both of these forms can cross the blood-brain barrier to reach your brain, the phospholipid form does so far more efficiently.
According to Patrick, people with APOE4 have a faulty nonesterified DHA transport system, and this may be why they’re at increased risk for Alzheimer’s. The good news is that DHA-lysoPC can bypass the tight junctions, thereby improving DHA transport, and for those with one or two APOE4 variants, taking the phospholipid form of DHA may therefore lower their risk of Alzheimer’s more effectively.
3. Choline Helps Fight Alzheimer’s Disease
Other recent research14 demonstrates the importance of choline for brain health and prevention of neurodegenerative diseases such as Alzheimer’s. Choline is a precursor to acetylcholine, a neurotransmitter required for the proper function of your brain and nervous system, playing a role in fetal brain development, memory, muscle control, mood and gene expression. As reported by Science Daily:15
“The study focuses on mice bred to display AD-like symptoms. Results showed that when these mice are given high choline in their diet, their offspring show improvements in spatial memory, compared with those receiving a normal choline regimen in the womb.
Remarkably, the beneficial effects of choline supplementation appear to be transgenerational, not only protecting mice receiving choline supplementation during gestation and lactation, but also the subsequent offspring of these mice. While this second generation received no direct choline supplementation, they nevertheless reaped the benefits of treatment, likely due to inherited modifications in their genes.”
Choline helps protect against Alzheimer’s by:
- Reducing your homocysteine level, an amino acid that has been shown to cause neurodegeneration and is involved in the formation of amyloid plaques, two hallmarks of Alzheimer’s. Choline converts homocysteine into methionine, which has a number of beneficial effects.
- Inhibiting microglia activation. Microglia cells clear debris from your brain, and while this is a crucial function, in Alzheimer’s the microglia have a tendency to become overactivated, causing inflammation in the brain that can result in the death of neurons. By reducing activation of microglia, choline can help protect Alzheimer’s patients from further brain damage.
4. Phosphatidylserine Boosts Cognitive Function
Phosphatidylserine is another supplement that can help improve cognitive function16 and protect against Alzheimer’s disease.17 Phosphatidylserine is an amino acid derivative that is highly prevalent in neural tissue and plays an important role in the cellular function in your brain.
While your body can synthesize it on its own, you can also get it through food (such as mackerel, cod, egg yolks and organ meats) and/or a phosphatidylserine complex supplement.18 Phosphatidylserine has a unique structure that makes it both hydrophilic, meaning it’s attracted to water and hydrophobic, or repelled by water.
With this structure, phospholipids are able to arrange themselves into a phospholipid bilayer — two parallel layers that form a major component of the human cell membranes. In brain cell membranes, the phospholipid bilayer acts as a “gatekeeper,” regulating the entry beneficial substances, basically nutrients, water and oxygen, while eliminating metabolic waste.19
In one study,20 supplementing with 400 mg of phosphatidylserine increased the speed of calculations done in short-term memory by 20% in a group of healthy adults. In another, it improved cognitive function of geriatric patients at a dosage of 300 mg per day for six months.21
Taken with DHA, it’s also been shown to improve behavior and short-term auditory memory in children with ADHD.22 In patients with Alzheimer’s, phosphatidylserine helps inhibit amyloid beta and interferon-gamma-induced microglial activation.23
5. Acetyl-L-Carnitine Protects Against Neurotoxic Insults
Acetyl-L-carnitine (ALCAR) has many beneficial effects on brain metabolism, protects against neurotoxic insults, and has been shown to benefit certain forms of depression. In one study,24 healthy mice given ALCAR for 25 days at a dose of about half a gram per kilo, were found to have increased levels of the neurotransmitters noradrenaline and serotonin. According to the authors, this is “consistent with ALCAR’s potential efficacy for depressive symptoms.”
In another study,25 ALCAR was found to improve the clinical condition of patients with degenerative cerebellar ataxia (a condition resulting in the loss of control of bodily movements). According to the authors, “statistically significant improvement of some symptoms and a slow progression of the disease in both groups of patients” were observed.
6. Vitamin D Protects Against Memory Loss
Activated vitamin D receptors increase nerve growth in your brain, and researchers have also located metabolic pathways for vitamin D in the hippocampus and cerebellum, areas involved in planning, information processing and memory formation.
According to research26 published in the Journal of Neurology, Neurosurgery and Psychiatry, low vitamin Dis associated with poorer brain function, and increasing levels may help keep older adults mentally fit. Vitamin D has also been shown to improve a number of brain disorders, including dementia and Alzheimer’s disease.27
In one six-year study,28 those with severe vitamin D deficiency were more than twice as likely to develop dementia and Alzheimer’s than those with higher levels. Even those with moderate deficiency had a 53% increased risk for all forms of dementia, and 69% increased risk for Alzheimer’s specifically. According to the authors, “Our results confirm that vitamin D deficiency is associated with a substantially increased risk of all-cause dementia and Alzheimer disease.”
The findings also suggest there’s a threshold level of circulating vitamin D, below which your risk for dementia increases. This threshold was found to be right around 20 ng/mL (50 nmol/L). Higher levels were associated with good brain health.
I recommend getting your vitamin D level tested twice a year, and taking whatever dosage required to achieve and maintain a vitamin D level between 60 and 80 ng/mL (150 and 200 nmol/L). Ideally, you’d want to raise your level by getting sensible sun exposure, but if you cannot, consider an oral vitamin D3 supplement balanced with magnesium and vitamin K2.
7. Vitamin B12 Deficiency Wreaks Havoc on Cognitive Function
Vitamin B12 is another important player. Research29 shows people with high levels of markers for vitamin B12 deficiency are more likely to score lower on cognitive tests and have a smaller total brain volume, which suggests a lack of B12 may contribute to brain shrinkage.
Mental fogginess and problems with memory are two of the top warning signs that you have vitamin B12 deficiency, and this is indicative of its importance for your brain health.
Finnish researchers have also found that people who consume foods rich in B12 may reduce their risk of Alzheimer’s in their later years.30 For each unit increase in the marker for vitamin B12 (holotranscobalamin) the risk of developing Alzheimer’s was reduced by 2%. Another study31 found that supplementing with B vitamins, including B12, helps to slow brain atrophy in elderly people with mild cognitive impairment.
Vitamin B12 deficiency is widespread and many have trouble absorbing this nutrient properly from food sources. Blood tests for vitamin B12 are not always a reliable indicator of B12 status, so watching for symptoms of deficiency and increasing your dietary and supplemental intake is a practical alternative to blood testing.
B12 is available in its natural form only in animal food sources such as seafood, beef, chicken, pork, milk and eggs. If you rarely or never consume these animal products, you’re at particularly high risk of B12 deficiency.
The good news is vitamin B12 supplementation is completely nontoxic and inexpensive, especially when compared to the cost of laboratory testing. I recommend an under-the-tongue fine mist spray, as this technology helps you absorb the vitamin into the fine capillaries under your tongue.
8. MCT Oil Boosts Brain Performance
One of the primary fuels your brain needs is glucose, which is converted into energy. Your brain actually manufactures its own insulin to convert glucose in your bloodstream into the food it needs to survive.
If your brain’s production of insulin decreases, your brain literally begins to starve, as it’s deprived of the glucose-converted energy it needs to function normally. This is what happens to Alzheimer’s patients — portions of their brain start to atrophy, or starve, leading to impaired functioning and eventual loss of memory, speech, movement and personality.
In effect, your brain can begin to atrophy from starvation if it becomes insulin resistant and loses its ability to convert glucose into energy. Fortunately, your brain is able to run on more than one type of energy supply. It can run on both glucose and ketones, and ketones are actually better.
Ketones are what your body produces (when it converts fat as opposed to glucose) into energy, and a primary source of ketone bodies are medium chain triglycerides (MCT). While coconut oil is one healthy option, MCT oil is a more concentrated source of ketones, so it tends to be more appropriate for clinical uses.
Most commercial brands of MCT oil contain a 50/50 combination of C8 and C10 fats (the “C number” stands for the carbon length of the MCT). My personal preference is straight C8 (caprylic acid), as it converts to ketones far more rapidly than do C10 fats, and will give you higher levels of ketones.
Ketones appear to be the preferred source of energy for the brain in people affected by diabetes, Alzheimer’s, Parkinson’s and maybe even ALS, because in these diseases, certain neurons have become insulin resistant or have lost the ability to efficiently utilize glucose. As a result, neurons slowly die off.
The introduction of ketones may rescue these neurons and they may still be able to survive and thrive. In multiple studies, ketones have been shown to be both neurotherapeutic and neuroprotective. They also appear to lower markers of systemic inflammation. As noted by Mental Health Daily:32
“In small scale human trials,33 MCT supplementation boosted cognition in individuals with cognitive impairment and mild forms of Alzheimer’s disease after just a single dose. While not everyone improved from the MCT treatment, those with certain genetics experienced notable improvement.”
9. Probiotics Feed Your Second Brain
As your “second brain,” the state of your gut also plays an important role in your neurological and psychological health. Probiotics have been shown to reduce symptoms of depression and decrease pathological hallmarks of Alzheimer’s, including amyloid plaques and tangles. In one study,34 the probiotic strain L. plantarum MTCC1325 was identified as having these “anti-Alzheimer’s properties.”
In another study,35 published in Frontiers in Aging Neuroscience, 60 elderly patients diagnosed with Alzheimer’s received either a placebo or a probiotic milk products containing Lactobacillus acidophilus, Lactobacillus casei, Bifidobacterium bifidum and Lactobacillus fermentum for 12 weeks.
At the beginning and end of the study, participants underwent a standardized cognitive assessment and a highly sensitive c-reactive protein test, which is a powerful marker of inflammation. As reported by neurologist Dr. David Perlmutter:36
“The results of the study were stunning. The placebo group showed an increase in hs-CRP, the inflammation marker, by an impressive 45%. In the group taking the probiotic, on the other hand, hs-CRP didn’t just stay the same, but actually declined by 18%, indicating a dramatic reduction in inflammation.
But here’s the truly exciting news. Over the 12 weeks, the patients in the placebo continued to decline mentally, as you might expect. Their MMSE score dropped from 8.47 to 8.00, a substantial reduction.
But the group on the inflammation reducing probiotics actually demonstrated, not a decline in brain function, but an actual improvement, with their MMSE scores going from 8.67 up to 10.57, and that’s a huge improvement. Again, not only was their mental decline stopped in its tracks, these individuals regained brain function!
The message here is that inflammation is directly determined by the health and diversity of our gut bacteria, and this has major implications in terms of brain health, function and disease resistance.”
- 1 Neurology March 25, 2014; 82(12)
- 2 World Health Organization. Dementia. Key Facts. September 2, 2021
- 3 Alzheimer’s and Dementia 2010 Nov;6(6):456-64
- 4 Nutritional Neuroscience 2008 Apr;11(2):75-83
- 5 Journal of Diabetes Investigation September 14, 2018 [Epub ahead of print]
- 6 BMC Cancer. 2018; 18: 1042
- 7 Nutrients 2011 May; 3(5): 529–554
- 8 British Journal of Psychiatry 2016; 2009: 192-201
- 9, 11 Medical Xpress January 8, 2019
- 10 J Lipid Res. 2019 Mar; 60(3): 566–578
- 12 FASEB Journal October 5, 2018
- 13 PR Newswire October 25, 2018
- 14 Molecular Psychiatry January 8, 2019
- 15 Science Daily January 8, 2019
- 16 Selfhacked.com November 20, 2018
- 17, 23 Free Radic Biol Med. 2007 Apr 1;42(7):945-54
- 18 Examine.com, Phosphatidylserine
- 19 Be Brain Fit, 6 Ways Phosphatidylserine Benefits Memory, Stress and Cognitive Decline
- 20 J Int Soc Sports Nutr. 2011; 8: 16
- 21 Aging 1993 Apr;5(2):123-33
- 22 J Hum Nutr Diet. 2014 Apr;27 Suppl 2:284-91
- 24 Neurochemistry International 2012 Jul;61(1):100-7
- 25 Clinical Neuropharmacology 2000 Mar-Apr;23(2):114-8
- 26 J Neurol Neurosurg Psychiatry. 2009 Jul;80(7):722-9
- 27 Neurology October 21, 2014 [Epub ahead of print]
- 28 Neurology August 6, 2014
- 29 Neurology. 2011 Sep 27;77(13):1276-82
- 30 Neurology. 2010 Oct 19;75(16):1402-3
- 31 PLOS ONE September 8, 2010
- 32 Mental Health Daily April 13, 2015
- 33 Nutritional Metabolism August 2009;10(6):31
- 34 Journal of Clinical and Diagnostic Research 2017 Aug; 11(8): KC01–KC05
- 35 Front. Aging Neurosci., 10 November 2016
- 36 Drperlmutter.com Reversing Alzheimer’s With Probiotics?
A Natural Way to Help Halt Disease-Causing Microorganisms?
Reproduced from original article:
https://articles.mercola.com/sites/articles/archive/2022/06/01/probiotics-for-dementia.aspx
The original Mercola article may not remain on the original site, but I will endeavor to keep it on this site as long as I deem it to be appropriate, and will not be bullied into removing it.
Analysis by Dr. Joseph Mercola Fact Checked June 01, 2022

STORY AT-A-GLANCE
- Probiotics can help improve cognitive function and ward off dementia, including Alzheimer’s
- Elderly Alzheimer’s patients who received a probiotic milk product containing Lactobacillus acidophilus, Lactobacillus casei, Bifidobacterium bifidum and Lactobacillus fermentum for 12 weeks significantly improved their cognition scores, while controls continued to decline
- The level of inflammatory markers also dropped by 18% in the probiotic treatment group, while inflammatory markers rose by 45% in the control group
- The Bifidobacterium breve strain A1 may be of particular use in Alzheimer’s treatment. Daily oral administration of B. breve A1 reduced the cognitive dysfunction normally induced by amyloid beta in mice
- Probiotics can inhibit neurodegeneration by modulating the inflammatory process, counteracting oxidative stress, modulating CNS functions mediated by bacteria-derived metabolites such as short-chain fatty acids, and inhibiting pathogenesis via alteration of gut microbiota composition
This article was previously published November 21, 2019, and has been updated with new information.
As your “second brain,” the state of your gut has been shown to play an important role in your neurological health. Importantly, studies have shown probiotics (beneficial bacteria) can help decrease pathological hallmarks of Alzheimer’s disease (AD), including amyloid plaques and tangles.1
One of the most impressive of these studies2 was published in Frontiers in Aging Neuroscience in 2016. Sixty elderly patients diagnosed with Alzheimer’s received either a placebo or a probiotic milk product containing Lactobacillus acidophilus, Lactobacillus casei, Bifidobacterium bifidum and Lactobacillus fermentum for 12 weeks.
At the beginning and end of the study, participants underwent a standardized cognitive assessment and a highly sensitive c-reactive protein test, which is a powerful marker of inflammation. As reported by neurologist Dr. David Perlmutter:3
“The results of the study were stunning. The placebo group showed an increase in hs-CRP, the inflammation marker, by an impressive 45 percent. In the group taking the probiotic, on the other hand, hs-CRP … declined by 18 percent, indicating a dramatic reduction in inflammation.
But here’s the truly exciting news. Over the 12 weeks, the patients in the placebo continued to decline mentally, as you might expect … But the group on the inflammation reducing probiotics actually demonstrated … improvement, with their MMSE [mini mental state examination] scores going from 8.67 up to 10.57, and that’s a huge improvement.
Again, not only was their mental decline stopped in its tracks, these individuals regained brain function! The message here is that inflammation is directly determined by the health and diversity of our gut bacteria, and this has major implications in terms of brain health, function, and disease resistance.”
Your Gut and Brain Are Linked
Since then, several other studies have been published, showing probiotics can help improve cognitive function and ward off dementia, including Alzheimer’s. While this may seem all too simple to be true, it makes perfect sense when you consider the deep connections that exist between your gut and your brain. As explained by Harvard Health:4
“Research shows that the gut and brain are connected, a partnership called the gut-brain axis. The two are linked through biochemical signaling between the nervous system in the digestive tract, called the enteric nervous system, and the central nervous system, which includes the brain.
The primary information connection between the brain and gut is the vagus nerve, the longest nerve in the body. The gut has been called a ‘second brain’ because it produces many of the same neurotransmitters as the brain does … What affects the gut often affects the brain and vice versa.
When your brain senses trouble — the fight-or-flight response — it sends warning signals to the gut, which is why stressful events can cause digestive problems like a nervous or upset stomach. On the flip side, flares of gastrointestinal issues like irritable bowel syndrome (IBS), Crohn’s disease, or chronic constipation may trigger anxiety or depression.”
Probiotic Prevents Amyloid-Beta-Induced Dysfunction
According to a 2017 study5 in Scientific Reports, the Bifidobacterium breve strain A1 may be of particular use in Alzheimer’s treatment. Using Alzheimer’s disease model mice, the researchers were able to confirm that daily oral administration of B. breve A1 reduced the cognitive dysfunction normally induced by amyloid beta. According to the authors:
“We also demonstrated that non-viable components of the bacterium or its metabolite acetate partially ameliorated the cognitive decline observed in AD mice.
Gene profiling analysis revealed that the consumption of B. breve A1 suppressed the hippocampal expressions of inflammation and immune-reactive genes that are induced by amyloid-β. Together, these findings suggest that B. breve A1 has therapeutic potential for preventing cognitive impairment in AD.”
One of the mechanisms behind these protective effects was found to be suppression of amyloid-beta-induced changes in gene expression in the hippocampus. In short, the bacterium had an ameliorating effect on amyloid-beta toxicity.
Interestingly, B. breve A1 did not actually alter the composition of the animals’ gut microbiota to any significant degree; rather, many of the benefits appear to be related to significantly raised blood levels of acetate, a byproduct of fermentation by gut bacteria. As explained by the authors:6
“One of the main functions of gut microbiota is the fermentation of dietary fibers in the gut and produce short-chain fatty acids (SCFAs), mainly acetate, propionate, and butyrate, which are the major end products of carbohydrate metabolism in Bifidobacteria.”
When looking at SCFA levels in the animals’ blood, the mice treated with B. breve A1 had significantly higher levels of acetate, but not propionate or butyrate, compared to controls.
Other microbiota-derived SCFAs may also play a role, however. A 2019 study7 found that rats given both probiotics and prebiotics performed significantly better on spatial memory tests, and this improvement was attributed to increased levels of brain-derived neurotrophic factor (BDNF).
Butyrate — a SCFA produced when gut bacteria ferment fiber — activates the secretion of BDNF. According to the authors, the improvement also correlated with “decreased levels of pro-inflammatory cytokines and better electrophysiological outcomes in the hippocampi.”
This led them to conclude that “the results indicated that the progression of cognitive impairment is indeed affected by changes in microbiota induced by probiotics and prebiotics.”
Probiotics Have Preventive and Therapeutic Potential for AD
The 2018 paper,8 “Probiotics for Preventing Cognitive Impairment in Alzheimer’s Disease,” points out that probiotics can inhibit the progression of neurodegeneration by:
- Modulating the inflammatory process9
- Counteracting oxidative stress10
- Modulating CNS functions mediated by bacteria-derived metabolites such as short-chain fatty acids11
- Ameliorating pathogenesis via alteration of gut microbiota composition12
Inflammation and oxidative stress modulation are primarily accomplished through the gut microbiota’s effects on your gut-brain axis, which in addition to your central nervous system (CNS) and enteric nervous system (ENS) also includes your autonomic nervous system, neuroendocrine system and immune system.13
These in turn are connected to various pathways involved in the regulation of immune function and metabolic homeostasis. These pathways include your vagus nerve and hypothalamic-pituitary adrenal pathway. According to “Probiotics for Preventing Cognitive Impairment in Alzheimer’s Disease:”14
“Accumulating evidence suggests that gut microbiota alterations can influence the progression of neurological disease and may be a major factor in the development of AD.
For instance, a recent preclinical study revealed a remarkable shift in the gut microbiota of APP transgenic mice as compared to healthy, wild-type mice … It was strongly advocated that a distinct microbial constitution in AD mice may contribute to amyloid deposition …
In addition, a clinical study characterizing the gut microbiota composition of AD subjects reveals decreased microbial diversity and changes in bacterial abundance compared with controls; these changes include decreased levels of Firmicutes and Bifidobacterium and increased levels of Bacteroidetes.”
The researchers speculate that gut microbiome alterations allowing for the colonization of pathogens that increase gut permeability can perturb the gut-brain axis, thereby raising your risk of Alzheimer’s. They cite research15 in which Enterobacteria infection was found to exacerbate the progression of Alzheimer’s as an example of this theory.
Immune Activation and Systemic Inflammation in AD
Many studies have suggested immune activation and low grade systemic and intestinal inflammation are important factors in Alzheimer’s, which can help explain why probiotics appear so beneficial. As noted in a 2018 publication:16
“… several different fecal and serum inflammation markers in correlation to intestinal bacterial strains were investigated in our recent study on the role of gut microbiota in patients with cognitive decline …
From a subgroup of 23 patients … out of 55 consecutive outpatients with symptoms of cognitive decline, intestinal bacterial taxa and immune system as well as inflammation biomarkers in serum and stool specimens were investigated.
Confirming our earlier findings … signs of immune activation could be detected … Most interestingly, a close correlation was found between fecal S100A12 and serum neopterin … indicating coincident low grade systemic and intestinal inflammation …
There was no influence of gender. These findings again underline the role of gut inflammation as a possible pathogenic cofactor in cognitive deterioration and dementia. In an earlier study … the potential role of pro-inflammatory … proteins in the pathogenesis of AD was described.
Circulating CRP, known to affect cognition negatively, was elevated in our series without clinical signs of acute infection … further indicating low grade inflammation … in this group of patients. We found pro-inflammatory Clostridium Cluster I significantly correlated with anti-inflammatory Faecalibacterium prausnitzii.
In a recent paper … the stool abundance of selected bacterial stool taxa including F. prausnitzii and the blood levels of pro- and anti-inflammatory cytokines in cognitively impaired patients and in a group of controls was measured.
Amyloid positive patients showed higher levels of pro-inflammatory cytokines compared with both controls and with amyloid negative patients. A possible causal relation between gut microbiota related inflammation and amyloidosis was suspected in this study …
All these findings together may indicate changes in the microbiota-gut-brain-axis correlated to neuroinflammation during cognitive decline. Because neuroinflammation is an early event in the pathogenesis of dementia, these markers may be important in the very beginning of this devastating process.”
The authors speculate that the increase in immune activation and inflammation seen in Alzheimer’s patients may be due to changes in microbiota that tends to occur with age.
They also note that “the role of probiotics in preventing dementia seems promising” and that further studies should be done to further tease out the exact mechanisms by which probiotics protect against neurodegeneration.
Alzheimer’s Prevention and Treatment Beyond Probiotics
While optimizing your gut microbiome is an important part of Alzheimer’s prevention and treatment, it needs to be part of a more comprehensive plan. Dr. Dale Bredesen, director of neurodegenerative disease research at the UCLA School of Medicine, discusses treatment alternatives in his book, “The End of Alzheimer’s: The First Program to Prevent and Reverse Cognitive Decline.”
Bredesen has identified dozens of variables that can have a significant influence on Alzheimer’s, and developed a treatment program based on those findings, called ReCODE.
In 2014, Bredesen published a paper detailing how leveraging 36 healthy lifestyle parameters reversed Alzheimer’s in 9 of 10 patients. This included the use of exercise, ketogenic diet, optimizing vitamin D and other hormones, increasing sleep, meditation, detoxification and eliminating gluten and processed foods. You can download Bredesen’s full-text case paper online, which details his program.17
As noted in a December 2018 article18 by Perlmutter, the largest class of medications prescribed for Alzheimer’s, called cholinesterase inhibitors, which break down acetylcholine, have actually been shown19 to accelerate cognitive decline! This, clearly, is the last thing you want, which means making lifestyle changes are all the more important, and the earlier you make them, the better.
As for how to nourish your gut microbiome, your best bet is to make your own fermented vegetables, which will provide plenty of beneficial bacteria for a fraction of the cost of a supplement.
- 1 Journal of Clinical and Diagnostic Research 2017 Aug; 11(8): KC01–KC05
- 2 Frontiers in Aging Neuroscience 2016 Nov 10;8:256
- 3 Drperlmutter.com Reversing Alzheimer’s With Probiotics?
- 4 Harvard Health Publishing, Probiotics May Help Boost Mood and Cognitive Function
- 5 Scientific Reports October 18, 2017; 7, Article Number 13510
- 6 Article Number 13510, B. breve A1 does not affect gut microbiota but significantly increases plasma acetate levels in AD model mice
- 7 Brain Circulation 2019; 3: 124-129
- 8 IntechOpen November 5, 2018, DOI: 10.5772/intechopen.79088
- 9 IntechOpen November 5, 2018, DOI: 10.5772/intechopen.79088, Section 5.1
- 10 IntechOpen November 5, 2018, DOI: 10.5772/intechopen.79088, Section 5.2
- 11 IntechOpen November 5, 2018, DOI: 10.5772/intechopen.79088, Section 5.3
- 12 IntechOpen November 5, 2018, DOI: 10.5772/intechopen.79088, Section 5.4
- 13 IntechOpen November 5, 2018, DOI: 10.5772/intechopen.79088, 3.1 Microbiota-gut-brain axis
- 14 IntechOpen November 5, 2018, DOI: 10.5772/intechopen.79088, 3.2 Gut microbiota alterations and Alzheimer’s disease
- 15 Nature Communications 2017 Jun 20;8(1):24
- 16 Frontiers in Aging Neuroscience 2018; 10: 54
- 17 Aging September 27, 2014; 6(9): 707-717
- 18 Drperlmutter.com December 7, 2018
- 19 JAMA Network Open 2018; 1(7): e184080 (PDF)