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依卡多曲对充血性心力衰竭犬急性容量扩张时的肾内效应。

Intrarenal effects of ecadotril during acute volume expansion in dogs with congestive heart failure.

作者信息

Solter P, Sisson D, Thomas W, Goetze L

机构信息

University of Illinois, College of Veterinary Medicine, Urbana-Champaign 61802, USA.

出版信息

J Pharmacol Exp Ther. 2000 Jun;293(3):989-95.

PMID:10869402
Abstract

Neutral endopeptidase 24.11 (NEP) inhibitors are known to have vascular, diuretic, and natriuretic effects that may be helpful in the treatment of congestive heart failure (CHF). Most NEP inhibitors may act principally through intrarenal mechanisms, which are not completely understood. The purpose of this study was to determine the principal renal effects of the NEP inhibitor ecadotril in dogs with progressive CHF induced by rapid ventricular pacing. Renal function was measured before, during, and after acute i.v. infusion of normal saline in a total of six dogs during normal cardiac function, early left ventricular dysfunction, and overt CHF. During overt CHF, each dog was treated with either ecadotril or placebo orally for 1 week. Parameters measured included glomerular filtration rate, renal blood flow, urine output, sodium clearance, sodium fractional excretion, and proximal and distal sodium reabsorption. Ecadotril treatment resulted in increased urine output, sodium clearance, and renal sodium excretion relative to placebo-treated controls. The principal intrarenal effect of ecadotril was decreased distal renal tubular sodium reabsorption. Both glomerular filtration rate and renal blood flow declined during overt CHF and were unaffected by ecadotril treatment. The results of this study are consistent with the principal action of ecadotril occurring by way of intrarenal events as opposed to changes in renal hemodynamics. The principal effect of ecadotril on distal tubular sodium reabsorption suggests that inhibition of NEP activity in the proximal renal tubules may allow increased binding of filtered atrial natriuretic peptide to natriuretic peptide receptor sites in the distal renal tubules and collecting ducts.

摘要

中性内肽酶24.11(NEP)抑制剂已知具有血管、利尿和利钠作用,可能有助于治疗充血性心力衰竭(CHF)。大多数NEP抑制剂可能主要通过肾内机制起作用,而这些机制尚未完全明确。本研究的目的是确定NEP抑制剂依卡多曲对快速心室起搏诱导的进行性CHF犬的主要肾脏作用。在正常心功能、早期左心室功能障碍和明显CHF期间,对总共6只犬在急性静脉输注生理盐水之前、期间和之后测量肾功能。在明显CHF期间,每只犬口服依卡多曲或安慰剂治疗1周。测量的参数包括肾小球滤过率、肾血流量、尿量、钠清除率、钠分数排泄以及近端和远端钠重吸收。与安慰剂治疗的对照组相比,依卡多曲治疗导致尿量增加、钠清除率增加和肾钠排泄增加。依卡多曲的主要肾内作用是远端肾小管钠重吸收减少。在明显CHF期间,肾小球滤过率和肾血流量均下降,且不受依卡多曲治疗的影响。本研究结果与依卡多曲的主要作用通过肾内事件发生而非肾血流动力学变化一致。依卡多曲对远端肾小管钠重吸收的主要作用表明,抑制近端肾小管中的NEP活性可能会使滤过的心房利钠肽与远端肾小管和集合管中的利钠肽受体位点的结合增加。

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