Endogenous Cardiotonic Steroids: Physiology, Pharmacology, and Novel Therapeutic Targets

被引:420
作者
Bagrov, Alexei Y. [1 ]
Shapiro, Joseph I. [2 ]
Fedorova, Olga V. [1 ]
机构
[1] NIA, Cardiovasc Sci Lab, NIH, 5600 Nathan Shock Dr, Baltimore, MD 21224 USA
[2] Univ Toledo, Dept Med, Toledo, OH 43606 USA
基金
美国国家卫生研究院;
关键词
DIGITALIS-LIKE COMPOUNDS; NA+-K+-ATPASE; OUABAIN-LIKE COMPOUND; DIGOXIN-LIKE IMMUNOREACTIVITY; ATRIAL-NATRIURETIC-PEPTIDE; BOVINE ADRENOCORTICAL-CELLS; PLASMALEMMAL NA/K-ATPASE; PROTEIN-KINASE-C; DIFFERENT SIGNALING PATHWAYS; NA+; K+-ATPASE ALPHA-SUBUNIT;
D O I
10.1124/pr.108.000711
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Endogenous cardiotonic steroids (CTS), also called digitalis-like factors, have been postulated to play important roles in health and disease for nearly half a century. Recent discoveries, which include the specific identification of endogenous cardenolide (endogenous ouabain) and bufadienolide (marinobufagenin) CTS in humans along with the delineation of an alternative mechanism by which CTS can signal through the Na+/K+-ATPase, have increased the interest in this field substantially. Although CTS were first considered important in the regulation of renal sodium transport and arterial pressure, more recent work implicates these hormones in the regulation of cell growth, differentiation, apoptosis, and fibrosis, the modulation of immunity and of carbohydrate metabolism, and the control of various central nervous functions and even behavior. This review focuses on the physiological interactions between CTS and other regulatory systems that may be important in the pathophysiology of essential hypertension, preeclampsia, endstage renal disease, congestive heart failure, and diabetes mellitus. Based on our increasing understanding of the regulation of CTS as well as the molecular mechanisms of these hormone increases, we also discuss potential therapeutic strategies.
引用
收藏
页码:9 / 38
页数:30
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