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糜酶抑制作为一种药理学靶点:在炎症性和功能性胃肠疾病中的作用?

Chymase inhibition as a pharmacological target: a role in inflammatory and functional gastrointestinal disorders?

机构信息

Department of Pharmacology and Therapeutics, University College Cork, Ireland Alimentary Pharmabiotic Centre, University College Cork, Ireland.

出版信息

Br J Pharmacol. 2012 Oct;167(4):732-40. doi: 10.1111/j.1476-5381.2012.02055.x.

Abstract

Chymase has been extensively studied with respect to its role in the pathophysiology of cardiovascular disease, and is notable for its role in the generation of angiotensin II, a mediator crucial in vascular remodelling. However, in more recent years, an association between chymase and several inflammatory diseases, including gastrointestinal (GI) disorders such as inflammatory bowel diseases (IBD) have been described. Such studies, to date, with respect to IBD at least, are descriptive in the clinical context; nonetheless, preclinical studies implicate chymase in the pathogenesis of gut inflammation. However, studies to elucidate the role of chymase in functional bowel disease are in their infancy, but suggest a plausible role for chymase in contributing to some of the phenotypic changes observed in such disorders, namely increased epithelial permeability. In this short review, we have summarized the current knowledge on the pathophysiological role of chymase and its inhibition with reference to inflammation and tissue injury outside of the GI tract and discussed its potential role in GI disorders. We speculate that chymase may be a novel therapeutic target in the GI tract, and as such, inhibitors of chymase warrant preclinical investigation in GI diseases.

摘要

糜酶在心血管疾病的病理生理学中的作用已经得到了广泛的研究,其在血管紧张素 II 生成中的作用尤为显著,血管紧张素 II 是血管重塑过程中的关键介质。然而,近年来,糜酶与包括胃肠道 (GI) 疾病在内的几种炎症性疾病之间的关联已经被描述。就目前而言,至少就炎症性肠病 (IBD) 而言,这些研究在临床背景下是描述性的;尽管如此,临床前研究表明糜酶参与了肠道炎症的发病机制。然而,阐明糜酶在功能性肠病中的作用的研究还处于起步阶段,但表明糜酶在导致这些疾病中观察到的一些表型变化方面可能发挥作用,即增加上皮通透性。在这篇简短的综述中,我们总结了糜酶在胃肠道以外的炎症和组织损伤的病理生理学作用及其抑制作用的最新知识,并讨论了其在胃肠道疾病中的潜在作用。我们推测糜酶可能是胃肠道的一个新的治疗靶点,因此,糜酶抑制剂值得在胃肠道疾病中进行临床前研究。

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