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新型非肽类口服生物可利用肾素抑制剂A-74273高剂量的作用

Effects of high doses of A-74273, a novel nonpeptidic and orally bioavailable renin inhibitor.

作者信息

Verburg K M, Polakowski J S, Kovar P J, Klinghofer V, Barlow J L, Stein H H, Mantei R A, Fung A K, Boyd S A, Baker W R

机构信息

Abbott Laboratories, Cardiovascular Research Division, Abbott Park, IL 60064.

出版信息

J Cardiovasc Pharmacol. 1993 Jan;21(1):149-55. doi: 10.1097/00005344-199301000-00022.

Abstract

Previous studies with peptidic renin inhibitors have shown that high intravenous (i.v.) doses can induce unexpectedly large decreases in blood pressure (BP) that appear to be independent of plasma renin inhibition. A-74273 represents a new class of potent and orally bioavailable nonpeptidic renin inhibitors. We evaluated the BP effects of this renin inhibitor administered orally (p.o.) or i.v. at high doses to conscious salt-depleted dogs. Administration of A-74273 at 30 and 60 mg/kg p.o. (n = 6 per dose) produced similar maximum reductions in BP (-40 +/- 4 vs. -46 +/- 5 mm Hg) despite the occurrence of greater plasma drug concentrations at the higher dose. Duration of hypotension, however, was increased (p < 0.05) from 9 h at 30 mg/kg to 18 h at 60 mg/kg. The initial depressor response to 10 and 30 mg/kg i.v. doses of A-74273 (n = 6 per dose) was comparable, although duration and overall BP response was greater at 30 mg/kg i.v. No BP responses to A-74273 were noted in salt-replete dogs (n = 5). The hypotension produced by 30 mg/kg p.o. A-74273 was completely reversed by norepinephrine (NE 5 micrograms/kg/min; n = 5) or isotonic saline (4 ml/min/kg, n = 5) infusion. These studies demonstrate that high doses of A-74273 result in predictable BP responses that are renin-dependent and reversible. Therefore, large decreases in BP with high doses is not an attribute common to all renin inhibitors but appears to be a function of the structural characteristics specific to a particular compound.

摘要

先前对肽类肾素抑制剂的研究表明,高静脉注射剂量可导致血压意外大幅下降,这似乎与血浆肾素抑制无关。A - 74273代表一类新型的强效且口服生物可利用的非肽类肾素抑制剂。我们评估了这种肾素抑制剂经口服或静脉高剂量给药对清醒的缺盐犬血压的影响。口服30和60mg/kg的A - 74273(每剂量n = 6)产生了相似的最大血压降低(-40±4与-46±5mmHg),尽管高剂量时血浆药物浓度更高。然而,低血压持续时间从30mg/kg时的9小时增加到60mg/kg时的18小时(p < 0.05)。静脉注射10和30mg/kg剂量的A - 74273(每剂量n = 6)的初始降压反应相当,尽管30mg/kg静脉注射时持续时间和总体血压反应更大。在盐充足的犬(n = 5)中未观察到对A - 74273的血压反应。口服30mg/kg的A - 74273产生的低血压可通过去甲肾上腺素(NE 5μg/kg/min;n = 5)或等渗盐水(4ml/min/kg,n = 5)输注完全逆转。这些研究表明,高剂量的A - 74273会导致可预测的、肾素依赖性且可逆的血压反应。因此,高剂量导致的血压大幅下降并非所有肾素抑制剂的共同特性,而似乎是特定化合物结构特征的作用。

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