4.5 Review

The Gut-Brain Axis: Two Ways Signaling in Parkinson's Disease

Journal

CELLULAR AND MOLECULAR NEUROBIOLOGY
Volume 42, Issue 2, Pages 315-332

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10571-021-01066-7

Keywords

Parkinson’ s disease; α -synuclein; Vagus nerve; Gastrointestinal tract; Enteric microbiota; Inflammation; Motor impairment

Funding

  1. University Grant Commission (Government of India)

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Parkinson's disease is a chronic and progressive neurological disorder involving the motor system, with its pathogenesis closely related to the gut microbiome and the gut-brain axis, which may influence the disease progression through various mechanisms. Understanding the interaction between the gut-brain axis, gut microbiota, and Parkinson's disease is crucial for the development of novel therapeutic and diagnostic approaches.
Parkinson's disease (PD) is a chronic, progressive and second most prevalent neurological disorder affecting the motor system. Cardinal motor impairment and alpha-synucleinopathy are the characteristic features of PD. Recently, it has been identified that the gut-brain axis is substantially regulated by the gut microbiome (GM) through an immunological, neuroendocrine, and neural mechanism. However, disturbance in the gut-microbiome-brain axis in PD might proceed to gastrointestinal manifestations intermittently leading to the motor system and the PD pathogenesis itself. The gut microbial toxins may induce the production of alpha-synuclein (alpha-syn) aggregates in the enteric nervous system (ENS), which may proliferate and propagate in a prion-like-manner through the vagus nerve to the central nervous system (CNS); supporting the hypothesis that, GM might play a pivotal role in PD pathogenesis. Overstimulated innate immune system due to intestinal bacterial overgrowth or gut dysbiosis and the enhanced intestinal permeability may persuade systemic inflammation, while the activation of enteric glial cells and enteric neurons may contribute to alpha-synucleinopathy. Gut microbiota can bear a significant impact on neurological outcomes such as learning, memory and cognition. In this review paper, we summarize how the alterations in gut microbiota and ENS inflammation are associated with PD pathogenesis. The evidence supporting the causative role played by gut-associated dysbiosis and microbial byproducts, in the onset of PD is also discussed. We have highlighted the landmark discoveries in the field of PD particularly focusing on the gut-brain axis. A better comprehension of the interaction between the gut-brain axis, gut microbiota, and PD can usher in novel therapeutic and diagnostic approaches.

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