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抑制心房利钠因子的代谢可导致慢性心力衰竭患者出现利尿和利钠作用。

Inhibition of the metabolism of atrial natriuretic factor causes diuresis and natriuresis in chronic heart failure.

作者信息

Northridge D B, Jardine A G, Findlay I N, Archibald M, Dilly S G, Dargie H J

机构信息

Department of Cardiology, Western Infirmary, Glasgow, Scotland.

出版信息

Am J Hypertens. 1990 Sep;3(9):682-7. doi: 10.1093/ajh/3.9.682.

Abstract

Atrial natriuretic factor (ANF) is a peptide hormone secreted by the heart that is degraded in vivo by endopeptidase 24:11 (atriopeptidase). UK 69,578 is a novel atriopeptidase inhibitor that raises plasma levels of ANF in animals and normal volunteers, with associated diuresis and natriuresis. This study examines the effects of UK 69,578 in patients with mild heart failure. UK 69,578 was administered as an intravenous infusion over 20 min in a placebo-controlled, cross-over study to six patients with stable (NYHA Class 2) chronic heart failure. The atriopeptidase inhibitor was well tolerated and no side effects were encountered. Mean baseline plasma ANF was elevated at 88 pg/mL (normal less than 50), and increased 2- to 5-fold after UK 69,578 administration. Plasma ANF did not change significantly following placebo. There was a marked diuresis after UK 69,578 compared to placebo. Urinary sodium excretion doubled for 4 to 6 h, but there was no significant rise in potassium excretion. There was no increase in plasma active renin concentration during the study period. Noninvasive hemodynamic monitoring revealed no significant changes in heart rate, systemic arterial blood pressure, or echocardiographic left ventricular dimensions. However, invasive measurements using a Swan-Ganz catheter demonstrated falls in mean right atrial and pulmonary artery wedge pressures after UK 69,578. There was no change in cardiac output. Thus, inhibition of endopeptidase 24:11 by UK 69,578 results in significant elevation of plasma ANF, with associated diuresis, natriuresis and venodilatation. The compound was well tolerated in these patients with mild chronic heart failure.

摘要

心房利钠因子(ANF)是一种由心脏分泌的肽类激素,在体内可被内肽酶24:11(心房肽酶)降解。UK 69,578是一种新型心房肽酶抑制剂,可提高动物和正常志愿者体内的ANF血浆水平,并伴有利尿和利钠作用。本研究探讨了UK 69,578对轻度心力衰竭患者的影响。在一项安慰剂对照的交叉研究中,对6例稳定(纽约心脏协会2级)慢性心力衰竭患者静脉输注UK 69,578,持续20分钟。该心房肽酶抑制剂耐受性良好,未出现副作用。平均基线血浆ANF升高至88 pg/mL(正常水平低于50),在给予UK 69,578后增加了2至5倍。给予安慰剂后血浆ANF无显著变化。与安慰剂相比,UK 69,578给药后出现明显利尿。尿钠排泄在4至6小时内增加了一倍,但钾排泄无显著增加。研究期间血浆活性肾素浓度未升高。无创血流动力学监测显示心率、体循环动脉血压或超声心动图左心室尺寸无显著变化。然而,使用Swan-Ganz导管进行的有创测量显示,给予UK 69,578后平均右心房和肺动脉楔压下降。心输出量无变化。因此,UK 69,578抑制内肽酶24:11可导致血浆ANF显著升高,并伴有利尿、利钠和静脉扩张作用。该化合物在这些轻度慢性心力衰竭患者中耐受性良好。

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