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皮质类固醇与心血管系统的昼夜节律

Corticosteroids and circadian rhythms in the cardiovascular system.

作者信息

Kanki Monica, Young Morag J

机构信息

Cardiovascular Endocrinology Laboratory, Baker Heart & Diabetes Institute, Melbourne, VIC, Australia; Cardiovascular Endocrinology Laboratory, Hudson Institute of Medical Research, Clayton, VIC, Australia; Department of Molecular & Translational Science, Monash University, Clayton, VIC, Australia.

Cardiovascular Endocrinology Laboratory, Baker Heart & Diabetes Institute, Melbourne, VIC, Australia; Cardiovascular Endocrinology Laboratory, Hudson Institute of Medical Research, Clayton, VIC, Australia; Department of Molecular & Translational Science, Monash University, Clayton, VIC, Australia; Department of Cardiometabolic Health, University of Melbourne, Melbourne, VIC, Australia.

出版信息

Curr Opin Pharmacol. 2021 Apr;57:21-27. doi: 10.1016/j.coph.2020.10.007. Epub 2020 Nov 15.

Abstract

The mineralocorticoid receptor (MR) plays a central role in cardiac physiological function and disease and is thus an attractive therapeutic target for patients with heart failure. However, the incidence of significant side effects from mineralocorticoid receptor antagonist (MRA) treatment has led to investigation of new mechanisms that may enhance MR targeted therapies. Recent studies have identified the circadian clock as a novel, reciprocal interacting partner of the MR in the heart. While the closely related glucocorticoid receptor (GR) and its ligand, cortisol (corticosterone in rodents), are established regulators of the circadian clock, new data suggest that the MR can also regulate circadian clock gene expression and timing. This review will discuss the role of the MR and its ligands in the regulation of the circadian clock in the heart and the implications of dysregulation of these systems for cardiac disease progression, and for MR activation.

摘要

盐皮质激素受体(MR)在心脏生理功能和疾病中起着核心作用,因此是心力衰竭患者颇具吸引力的治疗靶点。然而,盐皮质激素受体拮抗剂(MRA)治疗产生严重副作用的发生率促使人们研究可能增强MR靶向治疗的新机制。最近的研究已确定生物钟是心脏中MR的一种新型相互作用伙伴。虽然密切相关的糖皮质激素受体(GR)及其配体皮质醇(啮齿动物中的皮质酮)是生物钟的既定调节因子,但新数据表明MR也可调节生物钟基因表达和节律。本综述将讨论MR及其配体在心脏生物钟调节中的作用,以及这些系统失调对心脏病进展和MR激活的影响。

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