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缓激肽B2受体作为糖尿病肾病的一个靶点。

Bradykinin B2 receptors as a target in diabetic nephropathy.

作者信息

Doggrell Sheila A

机构信息

Division of Health Practice, Auckland University of Technology-Akoranga Campus, Auckland, New Zealand.

出版信息

Curr Opin Investig Drugs. 2006 Mar;7(3):251-5.

Abstract

Diabetic nephropathy is the leading cause of chronic renal failure in countries in the western world. Human polymorphism studies have suggested a nephroprotective effect that is mediated by bradykinin B2 receptors. Angiotensin converting enzyme (ACE) inhibitors and angiotensin receptor blockers have an additive nephroprotective effect in patients with diabetes, which may be due to ACE-inhibitor-mediated increases in the levels of bradykinin. There is also evidence from studies conducted in genetically altered mice to suggest that bradykinin is nephroprotective. Finally, evidence from animal models of nephropathy indicates that some of the beneficial effects of ACE inhibitors and vasopeptidase inhibitors are due to the action of bradykinin at B2 receptors. These data establish that stimulation of bradykinin B2 receptors is a target in diabetic nephropathy, and should provide impetus for the development of non-peptide, selective bradykinin B2 agonists.

摘要

在西方世界各国,糖尿病肾病是慢性肾衰竭的主要病因。人类多态性研究表明,缓激肽B2受体介导了一种肾脏保护作用。血管紧张素转换酶(ACE)抑制剂和血管紧张素受体阻滞剂对糖尿病患者具有附加的肾脏保护作用,这可能是由于ACE抑制剂介导的缓激肽水平升高所致。在基因改造小鼠中进行的研究也有证据表明缓激肽具有肾脏保护作用。最后,肾病动物模型的证据表明,ACE抑制剂和血管肽酶抑制剂的一些有益作用归因于缓激肽作用于B2受体。这些数据证实,刺激缓激肽B2受体是糖尿病肾病的一个治疗靶点,应该会推动非肽类选择性缓激肽B2激动剂的研发。

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