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Alzheimer's Infection Connection Strengthened


IMHO - This is researchers proving (again) what they already know, but clinicians and regulators are ignoring - while being complicit in the failed/falsified Amyloid Hypothesis.



Scientists have developed an artificial intelligence (AI) tool capable of diagnosing and predicting the risk of developing multiple health conditions — from ocular diseases to heart failure to Parkinson’s disease — all on the basis of people’s retinal images.


Summary: New research points to the possibility that the development of a pathobiome in the brain could play a role in Alzheimer’s and related dementias.


Studying brain samples, researchers discovered Alzheimer’s-affected brains had markedly different bacterial profiles compared to non-affected peers.


This suggests that specific bacterial sets in the brain could be predictors of Alzheimer’s disease. Moreover, these unique bacterial profiles were also found in brains afflicted by ALS, indicating potential implications in other neurological disorders.


Key Facts:


  • Alzheimer’s-afflicted brains revealed profoundly distinct bacterial profiles when compared to non-affected age-matched controls.

  • The bacterial sets identified in Alzheimer’s brains were also observed in ALS-affected brains, suggesting a broader neurological impact.

  • Current Alzheimer’s research is increasingly challenging the long-held “amyloid cascade hypothesis” in favor of a new “pathogen hypothesis,” focusing on bacterial, fungal, and viral factors.

Source: Drexel University


The human microbiome includes the genetic material of more than 100 trillion tiny microorganisms – fungi, yeast, bacteria, and even viruses, most of which hang out in our gastrointestinal tract to serve as guardians of our health. But when a healthy microbiome gives way to an imbalance — a “pathobiome” — any number of health problems can occur — from rheumatoid arthritis, to bacterial vaginosis.


New data published this month in the journal Frontiers in Cellular and Infection Microbiology, from researchers at Drexel’s College of Medicine, gives more evidence to the possibility that developing a pathobiome in the brain could cause some forms of Alzheimer’s and related dementias.


When biomes turn unhealthy, either by invasion of outside pathogens, or a major change in the relative numbers of the microbial species present, a dysbiosis, or imbalance in the microbiota, occurs. This dysbiosis can alter human metabolism and cause inflammation, which has been linked to the tissue damage seen in ulcerative colitis, rheumatoid arthritis and many other chronic inflammatory diseases.


Studying 130 samples from the donated brains of 32 people – 16 with Alzheimer’s and 16 age-matched controls without the disease, the Drexel researchers found bacterial flora in all the brains— but the Alzheimer’s brains showed profoundly different bacterial profiles compared to their age-matched controls.


The group used full-length 16s ribosomal RNA gene sequencing, a technique that can detect any and all bacterial species present in a sample. In this process, the researchers pinpointed disease-specific sets of bacteria in almost all of the Alzheimer’s-affected brains, suggesting these groups of bacteria are strong predictors of the disease.


The authors detected five brain microbiomes, four that are hypothesized to be present at different times in the evolution of the Alzheimer’s-afflicted brains. The authors said it is likely that the observed Alzheimer’s microbiomes evolve to become more pathogenic as the disease progresses with the later stages characterized as a pathobiome.


The authors hypothesize that the brain begins with a healthy biome, but as the disease develops, the healthy biome is supplanted as a new set of microbes replace the original healthy ones with the eventual emergence of the Alzheimer’s pathobiome.


Samples from both sets of brain samples were drawn from the frontal and temporal lobes and entorhinal cortex.


Based on the random distribution of microbiomes requiring delivery all over the brain, the results were consistent with failure in one or more of the brain’s networks; however it too soon to tell if the observed distribution patterns result from a leaky blood-brain barrier, the brain’s glymphatic system, or synaptonemal transmission that allowed bacteria, including Cutibacterium acnes (formerly called Proprionibacterium acnes), Methylobacterium, Bacillus, Caulobacter, Delftia, and Variovora to enter the brain.


In Alzheimer’s brain samples, the researchers noted, these pathogenic bacteria appeared to have overpowered and replaced Comamonas sp. bacteria, which are associated with a dementia-free brain.


“Perhaps destruction of the Comamonas bacteria, part of a healthy brain microbiome, is the first sign of impending dementia,” said Garth D. Ehrlich, PhD, a professor in the College of Medicine, who was a senior author of the paper.


“We’re now coming up with the questions to guide future studies, but the hypotheses are many. The culprit could be bacteria or something else – like fungi, parasites, or viruses – at the same time.”


When a patient has Alzheimer’s, they experience inflammation in the brain characterized by deposits of amyloid beta which are formed by an increase in the production of the Aβ peptide (an antimicrobial peptide, which is part of the innate immune response) resulting in amyloid plaques in the brain.


Similarly, Alzheimer’s is characterized by tau protein tangles found with the cells which are characterized by abnormal phosphorylation which ultimately lead to the destruction of synapses and neurons, but which have also been demonstrated to help stop the spread of pathogens in the brain.


These protein-oriented pathologies – known as the “amyloid cascade hypothesis”— have been the main focus of Alzheimer’s research for decades. Recently, studies are challenging that model by suggesting a role for bacteria, fungi and viruses, and immune system and brain inflammation, which some researchers call the “pathogen hypothesis.”


“Multiple studies have now shown the presence of bacteria in Alzheimer’s-afflicted brains,” said Jeffrey Lapides, PhD, an adjunct associate professor in the College of Medicine, and a senior author of the study.


“Perhaps plaques, whose constituents have anti-microbial properties in vitro, aren’t the direct cause of Alzheimer’s, but instead are a response to bacteria in the brain – some benign, some pathogenic, perhaps causing damage that has not yet resulted in cognitive deficits, making them part of the pathobiome.”


This unique set of bacteria found in the Alzheimer’s-afflicted brains are also commonly found in brains afflicted with the neurodegenerative disease amyotrophic lateral sclerosis, or ALS — suggesting that this set of bacteria may contribute to more than one neurological illness.


The next step for this research, according to the authors, is to study the possible contributions of other microbes and figure out what happened, physiologically, in the brain to make this microbiome change over time.


“The development of Alzheimer’s and other dementias is complex and likely involves the interaction of many systems,” said Ehrlich.


“I’m a believer in the more infections you get in the brain, the higher your risk of Alzheimer’s. There are many pathogens that likely increase the risk. This pathobiome is not the whole answer, but it’s a piece of the puzzle.”


The exact location of the problematic bacteria within the brain is also an open question, according to the team. Researchers need to know more precisely where the bacteria are to better understand the role they are playing.




The authors found that when an unhealthy pathobiome is located in the frontal lobe, the likelihood of Alzheimer’s disease being present is very high. It’s less likely to develop in the temporal lobe.


Despite the many unknowns, the authors said this is a significant step forward for studying the microbiome.


“The strength of our work is also to combine a breakthrough sequencing technology and the most advanced and innovative statistical approaches,” said lead author Yves Moné, PhD, a research associate in the College of Medicine. “Microbiome data analysis is notoriously challenging without any gold standard and this work could contribute significantly to the field of microbiome data analysis.”

 

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MORE RESEARCH:


TITLE: Mesenchymal stem cell derived-exosomes: a modern approach in translational medicine


Mesenchymal stem cells (MSCs) have captured great attention in regenerative medicine for over a few decades by virtue of their differentiation capacity, potent immunomodulatory properties, and their ability to be favorably cultured and manipulated. Recent investigations implied that the pleiotropic effects of MSCs is not associated to their ability of differentiation, but rather is mediated by the secretion of soluble paracrine factors.


Exosomes, nanoscale extracellular vesicles, are one of these paracrine mediators. Exosomes transfer functional cargos like:

  • miRNA and mRNA molecules,

  • peptides, proteins,

  • cytokines and lipids from MSCs to the recipient cells.

Exosomes participate in intercellular communication events and contribute to the healing of injured or diseased tissues and organs.


Studies reported that exosomes alone are responsible for the therapeutic effects of MSCs in numerous experimental models.


Therefore, MSC-derived exosomes can be manipulated and applied to establish a novel cell-free therapeutic approach for treatment of a variety of diseases including:

  • heart,

  • kidney,

  • liver,

  • immune and

  • neurological diseases, and

  • cutaneous wound healing.

In comparison with their donor cells, MSC-derived exosomes offer more stable entities and diminished safety risks regarding the administration of live cells, e.g. microvasculature occlusion risk.


This review discusses the exosome isolation methods invented and utilized in the clinical setting thus far and presents a summary of current information on MSC exosomes in translational medicine.


Link to 207 research papers that cited this one (above)



TITLE: The role of the paracrine/autocrine mediator endothelin-1 in regulation of cardiac contractility and growth


Endothelin-1 (ET-1) is a critical autocrine and paracrine regulator of cardiac physiology and pathology. Produced locally within the myocardium in response to diverse mechanical and neurohormonal stimuli, ET-1 acutely modulates cardiac contractility. During pathological cardiovascular conditions such as ischaemia, left ventricular hypertrophy and heart failure, myocyte expression and activity of the entire ET-1 system is enhanced, allowing the peptide to both initiate and maintain maladaptive cellular responses. Both the acute and chronic effects of ET-1 are dependent on the activation of intracellular signalling pathways, regulated by the inositol-trisphosphate and diacylglycerol produced upon activation of the ETA receptor. Subsequent stimulation of protein kinases C and D, calmodulin-dependent kinase II, calcineurin and MAPKs modifies the systolic calcium transient, myofibril function and the activity of transcription factors that coordinate cellular remodelling. The precise nature of the cellular response to ET-1 is governed by the timing, localization and context of such signals, allowing the peptide to regulate both cardiomyocyte physiology and instigate disease.


TITLE: Regener-Eyes® Ophthalmic Solution: A New Therapeutic Agent to Relieve Dryness of the Eye for Tear Hyperosmolarity-Induced Pathological Changes in the Eyes of Patients Suffering From Dry Eye Discomfort


Tear hyperosmolarity is an initial and crucial step in the development, progression and aggravation of dry eye discomfort. Decreased tear secretion or altered tear composition leads to tear film instability/imbalance which in Dry Eye (DE) patients results in abnormally rapid breakup of the tear film after blinking. Numerous structural changes in epithelial cells and mucin-producing goblet cells develop as a consequence of exposition of these cells to the hyperosmolar tears.


Tear hyperosmolarity causes oxidative stress, disruption of DNA repair system and induces DNA damage in the cells of ocular surface and lacrimal system, leading to their apoptosis. An injury of lacrimal glands results in decreased tear secretion, enabling the creation of “positive loop” that leads to the DE progression and aggravation. Accordingly, eye drops, which alleviate tear hyperosmolarity and restore tear homeostasis at corneal

surface, will break up vicious DEcycle and will relieve eye pain, irritation, discomfort, and vision disturbance in DE patients. RegenerEyes® Ophthalmic Solution is a hypotonic solution enriched with osmoprotectants (that address the hyperosmolarity of a tear film), which helps support tear stability and contribute to relieve dryness of the eye in DE patients. In this article, we summarized current knowledge and future perspectives about topical administration of Regener-Eyes® Ophthalmic Solution to relieve dryness of the eye in DE patients.


https://www.regenereyes.com/wp-content/uploads/2023/04/White-Paper_Regener-Eyes-Ophthalmic-Solution-A-New-Therapeutic_3.26.23.pdf

 

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