[May 12, 2023: Staff Writer, The Brighter Side of News]
Research reports for the first time a pathway that begins in the gut and ends with a potent pro-inflammatory toxin in brain cells contributing to the development of Alzheimer’s disease (AD). (CREDIT: Creative Commons)
In groundbreaking research, a novel pathway has been discovered by Dr. Yuhai Zhao and Dr. Walter J Lukiw from LSU Health New Orleans Neuroscience Center along with the Departments of Cell Biology and Anatomy, Neurology, and Ophthalmology.
This pathway, originating from the gut and concluding with a powerful pro-inflammatory toxin in brain cells, is implicated in the onset of Alzheimer's disease (AD). Moreover, the team has found a straightforward method to inhibit this process. The findings have been published in Frontiers in Neurology.
The team of scientists uncovered that a molecule, embodying an incredibly potent neurotoxin produced by microbes (lipopolysaccharide or LPS), stems from a Gram-negative bacterium known as Bacteroides fragilis, found in the human gastrointestinal (GI) tract. This molecule gives rise to a neurotoxin identified as BF-LPS.
When there's an insufficiency of this specific protein, it results in a gradual shrinkage of neuronal cells and eventually leads to their demise, a characteristic seen in neurons affected by Alzheimer's disease (AD). Moreover, the researchers highlight that maintaining an appropriate level of dietary fiber consumption could prevent this process from taking place.
The extremely potent neurotoxin BF-LPS is a naturally occurring waste product of microbial metabolism in our gut. The population of Bacteroides fragilis within our microbiome, the source of the neurotoxin BF-LPS, can be moderated by the intake of dietary fiber.
“Put another way, dietary-based approaches to balance the microorganisms in the microbiome may be an attractive means to modify the abundance, speciation, and complexity of enterotoxigenic forms of AD-relevant microbes and their potential for the pathological discharge of highly neurotoxic microbial-derived secretions that include BF-LPS and other forms of LPS,” Lukiw explains.
Analysis of the hsa-miRNA-30b-5p (miRNA-30b) interaction with the Homo sapien NF-L 3'-UTR. (CREDIT: Frontiers in Neurology)
The researchers ascertain that enhancing our comprehension of the relationship between the gastrointestinal (GI) tract and the Central Nervous System (CNS) axis, as well as the GI tract's microbiome and Alzheimer's disease, holds significant promise for pioneering novel diagnostic and therapeutic approaches in the medical treatment of Alzheimer's disease and other fatal, progressive, and age-associated neurodegenerative conditions.
For each experiment (using different batches of HNG cells) a control luciferase signal was generated that included separate controls with each analysis. (CREDIT: Frontiers in Neurology)
The National Institutes of Health states that Alzheimer's disease is the predominant diagnosis among individuals suffering from dementia. Furthermore, it ranks as the sixth highest cause of mortality among Americans.
LPS, present in brain cells affected with AD, has an inhibitory effect on NF-L expression. (CREDIT: Frontiers in Neurology)
LSU Health New Orleans incorporated the contributions of Drs. Vivian Jaber and Nathan Sharfman as co-authors. Aileen Pogue from Alchem Biotech Research based in Toronto, Canada, also participated as a co-author.
The research was supported by funding from LSU Health New Orleans, the Brown Foundation, the Joe and Dorothy Dorsett Innovation in Science Health Aging Award, and the National Institutes on Aging of the National Institutes of Health.