Schrier Robert W, Masoumi Amirali, Elhassan Elwaleed
University of Colorado Denver, Division of Renal Diseases and Hypertension, Denver, Colo., USA.
Blood Purif. 2009;27(1):28-32. doi: 10.1159/000167005. Epub 2009 Jan 23.
The pathogenesis of cardiac failure involves activation of the neurohumoral axis including stimulation of the sympathetic nervous system, the renin-angiotensin-aldosterone, and nonosmotic vasopressin systems. While these responses are critical in maintaining arterial pressure, they are associated with renal vasoconstriction, as well as sodium and water retention. In advanced circumstances, renal dysfunction and hyponatremia occur with cardiac failure. Even a modest rise in serum creatinine related to diminished renal function in heart failure patients is associated with increased risk for cardiovascular morbidity and mortality. Similarly, increased thirst and the nonosmotic stimulation of vasopressin in advanced cardiac failure leads to hyponatremia, which is also a major risk factor for mortality. Currently, V2 vasopressin receptor antagonists have been shown to correct hyponatremia in cardiac failure. One such agent, conivaptan, also is a V1 receptor antagonist which could theoretically benefit heart failure patients by decreasing cardiac afterload and remodeling. The effect of V2 receptor antagonists to correct hyponatremia in heart failure patients appears to be quite safe. However, to date no effect on mortality has been demonstrated.
心力衰竭的发病机制涉及神经体液轴的激活,包括交感神经系统、肾素 - 血管紧张素 - 醛固酮系统以及非渗透性血管加压素系统的刺激。虽然这些反应在维持动脉血压方面至关重要,但它们与肾血管收缩以及钠和水潴留有关。在病情进展时,心力衰竭会出现肾功能障碍和低钠血症。即使心力衰竭患者的血清肌酐因肾功能减退而有适度升高,也会增加心血管发病和死亡风险。同样,晚期心力衰竭时口渴增加以及血管加压素的非渗透性刺激会导致低钠血症,这也是死亡的主要危险因素。目前,V2血管加压素受体拮抗剂已被证明可纠正心力衰竭患者的低钠血症。其中一种药物考尼伐坦,也是一种V1受体拮抗剂,理论上可通过降低心脏后负荷和重塑来使心力衰竭患者受益。V2受体拮抗剂纠正心力衰竭患者低钠血症的效果似乎相当安全。然而,迄今为止尚未证明其对死亡率有影响。