肠道菌群通过调节吲哚-3-丙酸激活褪黑激素受体介导电针对缺血性脑卒中的快速耐受

Shan Li, Xiaoyong Zhao, Feihong Lin, Xuqing Ni, Xia Liu, Chang Kong, Xinyu Yao, Yunchang Mo, Qinxue Dai, Junlu Wang
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引用次数: 4

摘要

电针是治疗脑血管疾病的常用方法。本研究旨在从肠道微生态角度阐明脑缺血治疗的作用机制。我们通过小鼠模型和细胞培养研究了EA对大脑中动脉闭塞(MCAO)小鼠模型肠道菌群的影响及其代谢产物抗氧化活性的机制。粪便微生物群移植(FMT)被用来验证肠道微生物群的作用。通过代谢组学分析来表征EA + MCAO组和MCAO组小鼠的代谢谱差异。服用EA的小鼠(EA小鼠)比未服用EA的小鼠(非EA [NEA]小鼠)更能减轻脑损伤。EA和NEA小鼠的肠道微生物组成和代谢谱不同。特别是,EA或EA- fmt组小鼠的微生物群比MCAO或NEA-FMT组小鼠的微生物群产生更多的吲哚-3-丙酸(IPA)。在体内实验和N2a细胞缺氧、葡萄糖剥夺/再灌注模型实验中,我们证实IPA与靶细胞中特定的褪黑激素受体(MTRs)结合,并通过添加MTR抑制剂或敲除MTR1基因发挥抗氧化作用。EA可通过改善MCAO小鼠肠道菌群组成来预防缺血性脑卒中。此外,本研究揭示了一种不同于炎症/免疫的肠道菌群调节脑卒中的新机制,即肠道菌群通过影响IPA水平调节脑卒中。
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Gut Flora Mediates the Rapid Tolerance of Electroacupuncture on Ischemic Stroke by Activating Melatonin Receptor through Regulating Indole-3-Propionic Acid.
Electroacupuncture (EA) is commonly used to treat cerebrovascular diseases. This study aimed to clarify the mechanisms of action of treatments of cerebral ischemic stroke from the perspective of gut microecology. We used a mouse model and cell cultures to investigate the effects of EA on the intestinal microflora in mice models of middle cerebral artery occlusion (MCAO) and the mechanisms underlying the antioxidant activities of metabolites. Fecal microbiota transplantation (FMT) was used to validate the roles of gut microbiota. Metabolomic analysis was performed to characterize the metabolic profile differences between the mice in the EA + MCAO and MCAO groups. Gavaging with feces relieved brain damage in mice that received EA (EA mice) more than in mice that did not (non-EA [NEA] mice). The gut microbial composition and metabolic profiles of the EA and NEA mice were different. In particular, the microbiota from the mice in the EA or EA-FMT groups generated more indole-3-propionic acid (IPA) than the microbiota from the mice in the MCAO or NEA-FMT groups. We confirmed that IPA binds to specific melatonin receptors (MTRs) in target cells and exerts antioxidant effects by adding MTR inhibitors or knocking out the MTR1 gene in vivo and in the oxygen and glucose deprivation/reperfusion models of N2a cell experiments. EA can prevent ischemic stroke by improving the composition of intestinal microbiota in MCAO mice. Moreover, this study reveals a new mechanism of intestinal flora regulation of stroke that differs from inflammation/immunity, namely gut microbiota regulates stroke by affecting IPA levels.
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