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炎症性肠病药物:聚焦自噬

Inflammatory Bowel Disease Drugs: A Focus on Autophagy.

作者信息

Hooper Kirsty M, Barlow Peter G, Stevens Craig, Henderson Paul

机构信息

School of Life, Sport & Social Sciences, Edinburgh Napier University, Edinburgh, UK.

Child Life and Health, University of Edinburgh, Edinburgh, UK.

出版信息

J Crohns Colitis. 2017 Jan;11(1):118-127. doi: 10.1093/ecco-jcc/jjw127. Epub 2016 Jul 5.

Abstract

Inflammatory bowel disease [IBD] is characterized by chronic inflammation of the gastrointestinal tract. Medications such as corticosteroids, thiopurines, immunomodulators and biologic agents are used to induce and maintain remission; however, response to these drugs is variable and can diminish over time. Defective autophagy has been strongly linked to IBD pathogenesis, with evidence showing that enhancing autophagy may be therapeutically beneficial by regulating inflammation and clearing intestinal pathogens. It is plausible that the therapeutic effects of some IBD drugs are mediated in part through modulation of the autophagy pathway, with studies investigating a wide range of diseases and cell types demonstrating autophagy pathway regulation by these agents. This review will highlight the current evidence, both in vitro and in vivo, for the modulation of autophagy by drugs routinely used in IBD. A clearer understanding of their mechanisms of action will be invaluable to utilize these drugs in a more targeted and personalized manner in this diverse and often complex group of patients.

摘要

炎症性肠病(IBD)的特征是胃肠道的慢性炎症。诸如皮质类固醇、硫唑嘌呤、免疫调节剂和生物制剂等药物被用于诱导和维持缓解;然而,对这些药物的反应是可变的,并且会随着时间的推移而减弱。自噬缺陷与IBD发病机制密切相关,有证据表明增强自噬可能通过调节炎症和清除肠道病原体而具有治疗益处。一些IBD药物的治疗效果可能部分是通过调节自噬途径介导的,对多种疾病和细胞类型的研究表明这些药物可调节自噬途径。本综述将重点介绍目前在体外和体内关于IBD常用药物调节自噬的证据。更清楚地了解它们的作用机制对于在这群多样且往往复杂的患者中更有针对性和个性化地使用这些药物将非常宝贵。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d448/5175491/6350527207d5/jjw12701.jpg

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