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肾脏多巴胺信号异常与高血压:GRK4 的作用。

Abnormalities in renal dopamine signaling and hypertension: the role of GRK4.

机构信息

Division of Nephrology, Vanderbilt University School of Medicine, Nashville Veterans Affairs Hospital, Nashville, Tennessee 37232, USA.

出版信息

Curr Opin Nephrol Hypertens. 2012 Jan;21(1):61-5. doi: 10.1097/MNH.0b013e32834de2cb.

Abstract

PURPOSE OF REVIEW

This review will highlight the recent findings concerning the role of the intrarenal dopaminergic system in hypertension, especially the role of alterations in G-protein receptor kinase 4 (GRK4) activity.

RECENT FINDINGS

Recent studies highlight the importance of the intrarenal dopaminergic system in blood pressure regulation and how defects in dopamine signaling are involved in the development of hypertension. There are recent experimental models that definitively demonstrate that abnormalities in intrarenal dopamine production or receptor signaling can predispose to salt-sensitive hypertension and a dysregulated renin-angiotensin system. Furthermore, studies in experimental animal models and in humans with salt-sensitive hypertension implicate abnormalities in dopamine receptor regulation because of receptor desensitization resulting from increased GRK4 activity. Functional polymorphisms that predispose to increased basal GRK4 activity both decrease dopamine receptor activity and increase angiotensin II AT1 receptor activity and are associated with essential hypertension in a number of different human cohorts.

SUMMARY

The ongoing elucidation of this important regulatory pathway further emphasizes the importance of the kidney in maintenance of blood pressure control and may help to delineate the underlying mechanisms predisposing individuals or populations to increased risk for development of hypertension.

摘要

目的综述

本文将重点介绍肾内多巴胺能系统在高血压中的作用的最新发现,特别是 G 蛋白受体激酶 4(GRK4)活性改变的作用。

最新发现

最近的研究强调了肾内多巴胺能系统在血压调节中的重要性,以及多巴胺信号转导缺陷如何参与高血压的发生。最近有实验模型明确表明,肾内多巴胺产生或受体信号的异常可导致盐敏感型高血压和肾素-血管紧张素系统失调。此外,在盐敏感型高血压的实验动物模型和人类研究中,由于 GRK4 活性增加导致受体脱敏,多巴胺受体调节异常与高血压相关。功能多态性使基础 GRK4 活性增加,从而降低多巴胺受体活性,增加血管紧张素 II AT1 受体活性,与许多不同人群的原发性高血压有关。

总结

对这一重要调节途径的不断阐明进一步强调了肾脏在维持血压控制中的重要性,并可能有助于阐明导致个体或人群发生高血压风险增加的潜在机制。

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