Central regulation of blood pressure by the mineralocorticoid receptor

被引:47
作者
Gomez-Sanchez, Elise P. [1 ,3 ]
Gomez-Sanchez, Celso E. [2 ,3 ]
机构
[1] GV Sonny Montgomery VA Med Ctr, Res Serv, Jackson, MS 39216 USA
[2] GV Sonny Montgomery VA Med Ctr, Med Serv, Jackson, MS 39216 USA
[3] Univ Mississippi, Med Ctr, Dept Med, Jackson, MS 39216 USA
基金
美国国家卫生研究院;
关键词
Mineralocorticoid receptor; Brain; Hypertension; Aldosterone; Cortisol; Corticosterone; CENTRAL-NERVOUS-SYSTEM; ALDOSTERONE-SENSITIVE NEURONS; 11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE-2; HEART-FAILURE; DEOXYCORTICOSTERONE ACETATE; GLUCOCORTICOID-RECEPTOR; ANGIOTENSIN-II; MESSENGER-RNA; SMOOTH-MUSCLE; INTRACEREBROVENTRICULAR INFUSION;
D O I
10.1016/j.mce.2011.05.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Addition of mineralocorticoid receptor (MR) antagonists to standard therapy for heart failure, kidney disease, metabolic syndrome, and diabetes is increasing steadily in response to clinical trials demonstrating clear benefits. In addition to blocking deleterious activity of MR within the heart, vessels and kidneys. MR antagonists target MR in hemodynamic regulatory centers in the brain, thereby decreasing excessive sympathetic nervous system drive, vasopressin release, abnormal baroreceptor function, and circulating and tissue pro-inflammatory cytokines. However, brain MR are also involved with cognition, memory, affect and functions yet to be determined. Understanding specific central mechanisms involved in blood pressure regulation by MR is necessary for the development of agents to target downstream events specific to central hemodynamic regulation, not only to avoid the hypokalemia caused by inhibition of renal tubular MR, but also to avoid untoward long term effects of inhibiting brain MR that are not involved in blood pressure control. Published by Elsevier Ireland Ltd.
引用
收藏
页码:289 / 298
页数:10
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