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干扰盐皮质激素受体激活:过去、现在与未来。

Interfering with mineralocorticoid receptor activation: the past, present, and future.

作者信息

Dorrance Anne M

机构信息

Department of Pharmacology and Toxicology, Michigan State University, B340 Life Sciences 1355 Bogue Street, East Lansing, MI 48824 USA.

出版信息

F1000Prime Rep. 2014 Aug 1;6:61. doi: 10.12703/P6-61. eCollection 2014.

Abstract

Aldosterone is a potent mineralocorticoid produced by the adrenal gland. Aldosterone binds to and activates the mineralocorticoid receptor (MR) in a plethora of tissues, but the cardiovascular actions of aldosterone are of primary interest clinically. Although MR antagonists were developed as antihypertensive agents, they are now considered to be important therapeutic options for patients with heart failure. Specifically, blocking only the MR has proven to be a difficult task because of its similarity to other steroid receptors, including the androgen and progesterone receptors. This lack of specificity caused the use of the first-generation mineralocorticoid receptor antagonists to be fraught with difficulty because of the side effects produced by drug administration. However, in recent years, several advances have been made that could potentially increase the clinical use of agents that inhibit the actions of aldosterone. These will be discussed here along with some examples of the beneficial effects of these new therapeutic agents.

摘要

醛固酮是肾上腺产生的一种强效盐皮质激素。醛固酮在众多组织中与盐皮质激素受体(MR)结合并激活该受体,但醛固酮的心血管作用在临床上最为重要。尽管MR拮抗剂最初是作为抗高血压药物开发的,但现在它们被认为是心力衰竭患者的重要治疗选择。具体而言,由于MR与包括雄激素和孕激素受体在内的其他类固醇受体相似,仅阻断MR已被证明是一项艰巨的任务。这种缺乏特异性导致第一代盐皮质激素受体拮抗剂的使用因药物给药产生的副作用而充满困难。然而,近年来已经取得了一些进展,这些进展可能会增加抑制醛固酮作用的药物的临床应用。这里将讨论这些进展以及这些新治疗药物的一些有益效果的实例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01b1/4126546/f33c56275b53/biolrep-06-61-g001.jpg

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