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Current Neuropharmacology

Editor-in-Chief

ISSN (Print): 1570-159X
ISSN (Online): 1875-6190

General Review Article

Targeting Gut Dysbiosis and Microbiome Metabolites for the Development of Therapeutic Modalities for Neurological Disorders

Author(s): Matthew D. Wiefels, Emily Furar, Rebecca S. Eshraghi, Jeenu Mittal, Idil Memis, Moeed Moosa, Rahul Mittal and Adrien A. Eshraghi*

Volume 22, Issue 1, 2024

Published on: 27 March, 2023

Page: [123 - 139] Pages: 17

DOI: 10.2174/1570159X20666221003085508

Price: $65

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Abstract

The gut microbiota, composed of numerous species of microbes, works in synergy with the various organ systems in the body to bolster our overall health and well-being. The most well-known function of the gut microbiome is to facilitate the metabolism and absorption of crucial nutrients, such as complex carbohydrates, while also generating vitamins. In addition, the gut microbiome plays a crucial role in regulating the functioning of the central nervous system (CNS). Host genetics, including specific genes and single nucleotide polymorphisms (SNPs), have been implicated in the pathophysiology of neurological disorders, including Parkinson’s disease (PD), Alzheimer’s disease (AD), and autism spectrum disorder (ASD). The gut microbiome dysbiosis also plays a role in the pathogenesis of these neurodegenerative disorders, thus perturbing the gut-brain axis. Overproduction of certain metabolites synthesized by the gut microbiome, such as short-chain fatty acids (SCFAs) and p-cresyl sulfate, are known to interfere with microglial function and trigger misfolding of alpha-synuclein protein, which can build up inside neurons and cause damage. By determining the association of the gut microbiome and its metabolites with various diseases, such as neurological disorders, future research will pave the way for the development of effective preventive and treatment modalities.

Keywords: Gut microbiome, gut metabolite, gut dysbiosis, therapeutic modalities, neurological disorders, Alzheimer’s disease, Parkinson’s disease, Autism spectrum disorder.

Graphical Abstract
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