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脂肪组织与肠道菌群-肠-脑轴在脑发育和神经紊乱中的相互作用。

Cross-talk between adipose tissue and microbiota-gut-brain-axis in brain development and neurological disorder.

机构信息

Endocrinology Unit, Bioscience Department, Barkatullah University, Bhopal, Madhya Pradesh 462026, India.

Endocrinology Unit, Bioscience Department, Barkatullah University, Bhopal, Madhya Pradesh 462026, India.

出版信息

Brain Res. 2024 Dec 1;1844:149176. doi: 10.1016/j.brainres.2024.149176. Epub 2024 Aug 23.

Abstract

The gut microbiota is an important factor responsible for the physiological processes as well as pathogenesis of host. The communication between central nervous system (CNS) and microbiota occurs by different pathways i.e., chemical, neural, immune, and endocrine. Alteration in gut microbiota i.e., gut dysbiosis causes alteration in the bidirectional communication between CNS and gut microbiota and linked to the pathogenesis of neurological and neurodevelopmental disorder. Therefore, now-a-days microbiota-gut-brain-axis (MGBA) has emerged as therapeutic target for the treatment of metabolic disorder. But, experimental data available on MGBA from basic research has limited application in clinical study. In present study we first summarized molecular mechanism of microbiota interaction with brain physiology and pathogenesis via collecting data from different sources i.e., PubMed, Scopus, Web of Science. Furthermore, evidence shows that adipose tissue (AT) is active during metabolic activities and may also interact with MGBA. Hence, in present study we have focused on the relationship among MGBA, brown adipose tissue, and white adipose tissue. Along with this, we have also studied functional specificity of AT, and understanding heterogeneity among MGBA and different types of AT. Therefore, molecular interaction among them may provide therapeutic target for the treatment of neurological disorder.

摘要

肠道微生物群是负责宿主生理过程和发病机制的重要因素。中枢神经系统 (CNS) 和微生物群之间的通讯通过不同的途径发生,即化学、神经、免疫和内分泌。肠道微生物群的改变,即肠道菌群失调,导致 CNS 和肠道微生物群之间的双向通讯改变,并与神经和神经发育障碍的发病机制有关。因此,如今微生物群-肠道-大脑轴 (MGBA) 已成为治疗代谢紊乱的治疗靶点。但是,从基础研究中获得的关于 MGBA 的实验数据在临床研究中的应用有限。在本研究中,我们首先通过从不同来源(PubMed、Scopus、Web of Science)收集数据,总结了微生物群与大脑生理学和发病机制相互作用的分子机制。此外,有证据表明,脂肪组织 (AT) 在代谢活动中是活跃的,并且也可能与 MGBA 相互作用。因此,在本研究中,我们专注于 MGBA、棕色脂肪组织和白色脂肪组织之间的关系。除此之外,我们还研究了 AT 的功能特异性,以及理解 MGBA 和不同类型 AT 之间的异质性。因此,它们之间的分子相互作用可能为治疗神经障碍提供治疗靶点。

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