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Decoding the role of the gut microbiome in gut-brain axis, stress-resilience, or stress-susceptibility: A review

肠-脑轴 肠道菌群 失调 生物 微生物群 神经营养因子 神经科学 免疫系统 生物信息学 免疫学 医学 遗传学 受体
作者
Ranjay Kumar Sah,Amritasree Nandan,K V Athira,S. Kale Prashant,S. Sathianarayanan,Asha Jose,Baskar Venkidasamy,Shivraj Hariram Nile
出处
期刊:Asian Journal of Psychiatry [Elsevier]
卷期号:91: 103861-103861 被引量:8
标识
DOI:10.1016/j.ajp.2023.103861
摘要

Increased exposure to stress is associated with stress-related disorders, including depression, anxiety, and neurodegenerative conditions. However, susceptibility to stress is not seen in every individual exposed to stress, and many of them exhibit resilience. Thus, developing resilience to stress could be a big breakthrough in stress-related disorders, with the potential to replace or act as an alternative to the available therapies. In this article, we have focused on the recent advancements in gut microbiome research and the potential role of the gut-brain axis (GBA) in developing resilience or susceptibility to stress. There might be a complex interaction between the autonomic nervous system (ANS), immune system, endocrine system, microbial metabolites, and bioactive lipids like short-chain fatty acids (SCFAs), neurotransmitters, and their metabolites that regulates the communication between the gut microbiota and the brain. High fiber intake, prebiotics, probiotics, plant supplements, and fecal microbiome transplant (FMT) could be beneficial against gut dysbiosis-associated brain disorders. These could promote the growth of SCFA-producing bacteria, thereby enhancing the gut barrier and reducing the gut inflammatory response, increase the expression of the claudin-2 protein associated with the gut barrier, and maintain the blood-brain barrier integrity by promoting the expression of tight junction proteins such as claudin-5. Their neuroprotective effects might also be related to enhancing the expression of brain-derived neurotrophic factor (BDNF) and glucagon-like peptide (GLP-1). Further investigations are needed in the field of the gut microbiome for the elucidation of the mechanisms by which gut dysbiosis contributes to the pathophysiology of neuropsychiatric disorders.
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