Iyengar Srinivas, Feldman David S, Trupp Robin, Abraham William T
Division of Cardiovascular Medicine, The Ohio State University Heart Center, Columbus, Oh 43210-1252, USA.
Expert Opin Pharmacother. 2004 Apr;5(4):901-7. doi: 10.1517/14656566.5.4.901.
Nesiritide (Natrecor) is a recombinant form of the human B-type natriuretic peptide (BNP) that has been shown, through several studies, to have beneficial natriuretic, diuretic and vasodilatory effects in the treatment of congestive heart failure (CHF). Nesiritide mimics the actions of endogenous BNP by binding to and stimulating receptors in the heart, kidney and vasculature. Nesiritide functions as both a potent venous and arterial vasodilator and has been shown to improve cardiac haemodynamics more rapidly and to a greater extent than intravenous nitroglycerin, as well as having fewer side effects. When compared in an open-label trial, nesiritide has also been shown to be less proarrhythmic than dobutamine. The major adverse effect of nesiritide, as with other vasodilators, is symptomatic hypotension, which occurred infrequently in clinical trials. Overall, nesiritide represents an effective and safe therapeutic option for the treatment of decompensated CHF.
奈西立肽(Natrecor)是重组人B型利钠肽(BNP),多项研究表明,其在治疗充血性心力衰竭(CHF)方面具有有益的利钠、利尿和血管舒张作用。奈西立肽通过与心脏、肾脏和血管中的受体结合并刺激这些受体,模拟内源性BNP的作用。奈西立肽兼具强效静脉和动脉血管舒张剂的功能,已证明其改善心脏血流动力学的速度比静脉注射硝酸甘油更快、程度更大,且副作用更少。在一项开放标签试验中进行比较时,奈西立肽也显示出比多巴酚丁胺更少引起心律失常。与其他血管舒张剂一样,奈西立肽的主要不良反应是症状性低血压,在临床试验中发生率较低。总体而言,奈西立肽是治疗失代偿性CHF的一种有效且安全的治疗选择。