Microbiota-gut-brain axis in health and neurological disease: Interactions between gut microbiota and the nervous system

Author: Yuhong He1,2, Ke Wang1, Niri Su2, Chongshan Yuan2, Naisheng Zhang2, Xiaoyu Hu2, Yunhe Fu2, Feng Zhao1
Affiliation: <sup>1</sup> Department of Operating Room, China-Japan Union Hospital of Jilin University, Changchun, Jilin, China. <sup>2</sup> Department of Clinical Veterinary Medicine, College of Veterinary Medicine, Jilin University, Changchun, Jilin, China.
Conference/Journal: J Cell Mol Med
Date published: 2024 Sep 1
Other: Volume ID: 28 , Issue ID: 18 , Pages: e70099 , Special Notes: doi: 10.1111/jcmm.70099. , Word Count: 202


Along with mounting evidence that gut microbiota and their metabolites migrate endogenously to distal organs, the 'gut-lung axis,' 'gut-brain axis,' 'gut-liver axis' and 'gut-renal axis' have been established. Multiple animal recent studies have demonstrated gut microbiota may also be a key susceptibility factor for neurological disorders such as Alzheimer's disease, Parkinson's disease and autism. The gastrointestinal tract is innervated by the extrinsic sympathetic and vagal nerves and the intrinsic enteric nervous system, and the gut microbiota interacts with the nervous system to maintain homeostatic balance in the host gut. A total of 1507 publications on the interactions between the gut microbiota, the gut-brain axis and neurological disorders are retrieved from the Web of Science to investigate the interactions between the gut microbiota and the nervous system and the underlying mechanisms involved in normal and disease states. We provide a comprehensive overview of the effects of the gut microbiota and its metabolites on nervous system function and neurotransmitter secretion, as well as alterations in the gut microbiota in neurological disorders, to provide a basis for the possibility of targeting the gut microbiota as a therapeutic agent for neurological disorders.

Keywords: gut microbiota; microbiota–gut–brain axis; nervous system; neurotransmitter.

PMID: 39300699 DOI: 10.1111/jcmm.70099