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Lactobacillus murinus alleviate intestinal ischemia/reperfusion injury through promoting the release of interleukin-10 from M2 macrophages via Toll-like receptor 2 signaling.鼠李糖乳杆菌通过 Toll 样受体 2 信号通路促进 M2 巨噬细胞释放白细胞介素-10 缓解肠道缺血再灌注损伤。
Microbiome. 2022 Mar 3;10(1):38. doi: 10.1186/s40168-022-01227-w.
2
Propionate alleviates myocardial ischemia-reperfusion injury aggravated by Angiotensin II dependent on caveolin-1/ACE2 axis through GPR41.丙酸通过 GPR41 减轻血管紧张素 II 依赖性 Cav-1/ACE2 轴加重的心肌缺血再灌注损伤。
Int J Biol Sci. 2022 Jan 1;18(2):858-872. doi: 10.7150/ijbs.67724. eCollection 2022.
3
Aberrant enteric neuromuscular system and dysbiosis in amyotrophic lateral sclerosis.肌萎缩侧索硬化症中的肠道神经肌肉系统异常和微生态失调。
Gut Microbes. 2021 Jan-Dec;13(1):1996848. doi: 10.1080/19490976.2021.1996848.
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Polyamine metabolism links gut microbiota and testicular dysfunction.多胺代谢将肠道微生物群与睾丸功能障碍联系起来。
Microbiome. 2021 Nov 11;9(1):224. doi: 10.1186/s40168-021-01157-z.
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Intestinal microbiota shapes gut physiology and regulates enteric neurons and glia.肠道微生物群塑造肠道生理学,并调节肠神经元和神经胶质细胞。
Microbiome. 2021 Oct 26;9(1):210. doi: 10.1186/s40168-021-01165-z.
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Gut Microbial Metabolite Pravastatin Attenuates Intestinal Ischemia/Reperfusion Injury Through Promoting IL-13 Release From Type II Innate Lymphoid Cells IL-33/ST2 Signaling.肠道微生物代谢产物普伐他汀通过促进 II 型先天淋巴细胞释放白细胞介素 13 来减轻肠缺血/再灌注损伤:IL-33/ST2 信号通路。
Front Immunol. 2021 Sep 28;12:704836. doi: 10.3389/fimmu.2021.704836. eCollection 2021.
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Synergistic Protective Effect of Konjac Mannan Oligosaccharides and on Intestinal Epithelial Barrier Dysfunction in Caco-2 Cell Model and Mice Model of Lipopolysaccharide Stimulation.魔芋低聚糖和 对脂多糖刺激 Caco-2 细胞模型及小鼠模型肠上皮屏障功能障碍的协同保护作用。
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Distinct B cell subsets in Peyer's patches convey probiotic effects by Limosilactobacillus reuteri.派尔集合淋巴结中不同的B细胞亚群通过罗伊氏乳杆菌发挥益生菌作用。
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Autophagy and Host Defense in Nontuberculous Mycobacterial Infection.非结核分枝杆菌感染中的自噬与宿主防御
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Microbiota metabolite butyrate constrains neutrophil functions and ameliorates mucosal inflammation in inflammatory bowel disease.微生物代谢产物丁酸盐可限制中性粒细胞功能并改善炎症性肠病的黏膜炎症。
Gut Microbes. 2021 Jan-Dec;13(1):1968257. doi: 10.1080/19490976.2021.1968257.

肠道微生物群与肠道缺血/再灌注损伤的关系。

Association of Gut Microbiota With Intestinal Ischemia/Reperfusion Injury.

机构信息

Department of Anesthesiology, Taihe Hospital, Hubei University of Medicine, Shiyan, China.

Department of Surgical Nursing, Taihe Hospital, Hubei University of Medicine, Shiyan, China.

出版信息

Front Cell Infect Microbiol. 2022 Jul 12;12:962782. doi: 10.3389/fcimb.2022.962782. eCollection 2022.

DOI:10.3389/fcimb.2022.962782
PMID:35903197
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9314564/
Abstract

Intestinal ischemia/reperfusion (II/R) is a common acute and critical condition in clinical practice with a high mortality rate. However, there is still a lack of effective prevention and treatment measures for II/R injury. The role of the gut microbiota in II/R has attracted widespread attention. Recent evidence has demonstrated that the gut microbiota plays a pivotal role in the occurrence, development, and prognosis of II/R. Therefore, maintaining the homeostasis of gut microbiota and its metabolites may be a potential strategy for the treatment of II/R. This review focuses on the importance of crosstalk between the gastrointestinal ecosystem and II/R to highlight II/R-induced gut microbiota signatures and potential applications of microbial-based therapies in II/R. This will also provide potentially effective biomarkers for the prediction, diagnosis and treatment of II/R.

摘要

肠缺血/再灌注(II/R)是临床实践中常见的急性危重症,死亡率高。然而,目前对于 II/R 损伤仍然缺乏有效的预防和治疗措施。肠道微生物群在 II/R 中的作用引起了广泛关注。最近的证据表明,肠道微生物群在 II/R 的发生、发展和预后中起着关键作用。因此,维持肠道微生物群及其代谢物的平衡可能是治疗 II/R 的一种潜在策略。本综述重点关注胃肠道生态系统与 II/R 之间的相互作用的重要性,以突出 II/R 诱导的肠道微生物群特征和基于微生物的疗法在 II/R 中的潜在应用。这也将为 II/R 的预测、诊断和治疗提供潜在的有效生物标志物。