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(前体)肾素受体:它们具有生物学相关性吗?

(Pro)renin receptors: are they biologically relevant?

作者信息

Danser A H Jan

机构信息

Division of Pharmacology, Vascular and Metabolic Diseases, Department of Internal Medicine, Rotterdam, The Netherlands.

出版信息

Curr Opin Nephrol Hypertens. 2009 Jan;18(1):74-8. doi: 10.1097/MNH.0b013e3283196aaf.

Abstract

PURPOSE OF REVIEW

The recent introduction of a renin inhibitor, aliskiren, into the clinical arena has revived interest in renin and its precursor prorenin. In addition, a renin-binding and prorenin-binding receptor has been found, which not only activates prorenin but also induces angiotensin-independent signaling. This review addresses the question of whether this receptor has any biological relevance.

RECENT FINDINGS

Prorenin is the preferred agonist of the (pro)renin receptor. When bound to the receptor, prorenin undergoes a conformational change allowing it to display full enzymatic activity. Receptor activation by renin/prorenin triggers the mitogen-activated protein kinase-extracellular signal-regulated kinase 1/2 signaling pathway, and human (pro)renin receptor transgenic rats develop glomerulosclerosis and hypertension in the absence of changes in renin or angiotensin. Aliskiren prevents angiotensin I generation by receptor-bound prorenin but does not block signaling. Conflicting results have been obtained with the putative (pro)renin receptor antagonist 'handle region peptide', suggesting that its efficacy depends on experimental conditions.

SUMMARY

Although it is tempting to speculate that the (pro)renin receptor is the missing link providing a role for prorenin in tissue angiotensin generation, the discrepant results with handle region peptide and the lack of clinical studies with (pro)renin receptor blockers do not yet firmly support such a role.

摘要

综述目的

肾素抑制剂阿利吉仑最近被引入临床领域,这重新引发了人们对肾素及其前体肾素原的兴趣。此外,还发现了一种肾素结合和肾素原结合受体,它不仅能激活肾素原,还能诱导不依赖血管紧张素的信号传导。本综述探讨了该受体是否具有任何生物学相关性的问题。

最新发现

肾素原是(前)肾素受体的首选激动剂。当与受体结合时,肾素原会发生构象变化,使其展现出完整的酶活性。肾素/肾素原激活受体可触发丝裂原活化蛋白激酶-细胞外信号调节激酶1/2信号通路,并且人类(前)肾素受体转基因大鼠在肾素或血管紧张素无变化的情况下会出现肾小球硬化和高血压。阿利吉仑可阻止受体结合的肾素原生成血管紧张素I,但不阻断信号传导。使用假定的(前)肾素受体拮抗剂“柄区肽”得到了相互矛盾的结果,这表明其疗效取决于实验条件。

总结

尽管很容易推测(前)肾素受体是肾素原在组织血管紧张素生成中发挥作用的缺失环节,但柄区肽的结果不一致以及缺乏(前)肾素受体阻滞剂的临床研究尚未有力支持这一作用。

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