Weber K T, Villarreal D
Department of Internal Medicine, University of Missouri, Columbia 65212.
Am J Cardiol. 1993 Jan 21;71(3):3A-11A. doi: 10.1016/0002-9149(93)90238-8.
The pathophysiologic cycle that links myocardial failure with the appearance of congestive heart failure is not fully understood. It is clear, however, that an activation of several neurohormonal systems and the interplay between kidneys, adrenal glands, and heart contribute to abnormal sodium and water homeostasis. Aldosterone, the body's most potent mineralocorticoid hormone, contributes to intravascular and extravascular volume expansion, and thus to the appearance of symptomatic failure. Antialdosterone therapy in patients with secondary hyperaldosteronism due to heart failure must achieve one or more of the following goals: reduce or, preferably, normalize plasma aldosterone levels by limiting synthesis; antagonize the renal and systemic effects of aldosterone at its receptor sites; and eliminate or minimize the multiple stimuli to aldosterone secretion.
将心肌衰竭与充血性心力衰竭的出现联系起来的病理生理循环尚未完全明了。然而,很明显,几种神经激素系统的激活以及肾脏、肾上腺和心脏之间的相互作用导致了钠和水平衡异常。醛固酮是人体最有效的盐皮质激素,它会导致血管内和血管外容量增加,进而导致症状性心力衰竭的出现。对于因心力衰竭导致继发性醛固酮增多症的患者,抗醛固酮治疗必须实现以下一个或多个目标:通过限制合成来降低或最好使血浆醛固酮水平正常化;在醛固酮的受体部位拮抗其对肾脏和全身的作用;消除或尽量减少对醛固酮分泌的多种刺激。