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依普利酮抑制醛固酮诱导的肾环氧合酶表达。

Eplerenone inhibits aldosterone-induced renal expression of cyclooxygenase.

机构信息

Department of Pharmacology/Toxicology, Morehouse School of Medicine, Atlanta, Georgia 30310, USA.

出版信息

J Renin Angiotensin Aldosterone Syst. 2012 Sep;13(3):353-9. doi: 10.1177/1470320312443911. Epub 2012 May 3.

Abstract

INTRODUCTION

The upregulation of cyclooxygenase (COX) expression by aldosterone (ALDO) or high salt diet intake is very interesting and complex in the light of what is known about the role of COX in renal function. Thus, in this study, we hypothesize that apocynin (APC) and/or eplerenone (EPL) inhibit ALDO/salt-induced kidney damage by preventing the production of prostaglandin E₂ (PGE₂).

METHODS

Dahl salt-sensitive rats on either a low-salt or high-salt diet were treated with ALDO (0.2 mg pellet) in the presence of EPL (100 mg/kg/day) or APC (1.5 mM). Indirect blood pressure, prostaglandins and ALDO levels and histological changes were measured.

RESULTS

Cyclooxygenase-2 (COX-2) levels were upregulated in the renal tubules and peritubular vessels after high-salt intake, and APC attenuated renal tubular COX-2 protein expression induced by ALDO. Plasma PGE₂ levels were significantly reduced by ALDO in the rats fed a low-salt diet when compared to rats fed a high-salt diet. PGE₂ was blocked by EPL but increased in the presence of APC.

CONCLUSIONS

The beneficial effects of EPL may be associated with an inhibition of PGE₂. The mechanism underlying the protective effects of EPL is clearly distinct from that of APC and suggests that these agents can have differential roles in cardiovascular disease.

摘要

简介

醛固酮(ALDO)或高盐饮食摄入上调环氧化酶(COX)表达非常有趣和复杂,考虑到 COX 在肾功能中的作用。因此,在这项研究中,我们假设白杨素(APC)和/或依普利酮(EPL)通过防止前列腺素 E₂(PGE₂)的产生来抑制 ALDO/盐诱导的肾脏损伤。

方法

低盐或高盐饮食的 Dahl 盐敏感大鼠用 ALDO(0.2 mg 微球)处理,同时给予 EPL(100 mg/kg/天)或 APC(1.5 mM)。测量间接血压、前列腺素和 ALDO 水平以及组织学变化。

结果

高盐摄入后,肾小管和肾小管周围血管中的 COX-2 水平上调,APC 减弱了 ALDO 诱导的肾小管 COX-2 蛋白表达。与高盐饮食组相比,低盐饮食组大鼠的血浆 PGE₂ 水平因 ALDO 而显著降低。EPL 阻断了 PGE₂,但 APC 存在时 PGE₂增加。

结论

EPL 的有益作用可能与 PGE₂ 的抑制有关。EPL 的保护作用的机制显然与 APC 不同,这表明这些药物在心血管疾病中可能具有不同的作用。

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