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健康志愿者中血管紧张素II受体拮抗剂TCV-116的特性研究。

Characterization of the angiotensin II receptor antagonist TCV-116 in healthy volunteers.

作者信息

Delacrétaz E, Nussberger J, Biollaz J, Waeber B, Brunner H R

机构信息

Division of Hypertension, University Hospital, Lausanne, Switzerland.

出版信息

Hypertension. 1995 Jan;25(1):14-21. doi: 10.1161/01.hyp.25.1.14.

Abstract

The purpose of this study was to assess the inhibitory effect of TCV-116, an orally active angiotensin II (Ang II) antagonist, on the pressor action of exogenous Ang II and to determine the compensatory rise in plasma renin activity and Ang II levels. Twenty-three male volunteers were treated for 8 days in a double-blind fashion with either placebo or TCV-116 (1, 2, or 4 mg PO daily) and challenged on the first, fourth, and eighth days with repeated bolus injections of Ang II. An additional 4 subjects received 8 mg PO daily in a single-blind fashion. The inhibitory effect on the systolic blood pressure response to Ang II was long lasting and clearly dose related. Six hours after 4 mg TCV-116, the systolic blood pressure response to a given dose of Ang II was reduced to 40 +/- 4% and 35 +/- 8% of baseline value on days 1 and 8, respectively. TCV-116 induced a dose-related increase in plasma renin activity and Ang II levels that was more pronounced on the eighth than on the first day of drug administration. Despite this compensatory mechanism, the relation between the time-integrated systolic blood pressure response to Ang II and the time-integrated CV-11974 levels, the active metabolite of TCV-116, was not different between days 1 and 8. In conclusion, TCV-116 appears to be a well-tolerated, orally active, potent, and long-lasting antagonist of Ang II in men.

摘要

本研究的目的是评估口服活性血管紧张素II(Ang II)拮抗剂TCV-116对外源性Ang II升压作用的抑制效果,并确定血浆肾素活性和Ang II水平的代偿性升高。23名男性志愿者以双盲方式接受为期8天的治疗,分别给予安慰剂或TCV-116(每日口服1、2或4毫克),并在第1、4和8天通过重复推注Ang II进行激发试验。另外4名受试者以单盲方式每日口服8毫克。对Ang II引起的收缩压反应的抑制作用持久且明显与剂量相关。服用4毫克TCV-116后6小时,在第1天和第8天,对给定剂量Ang II的收缩压反应分别降至基线值的40±4%和35±8%。TCV-116导致血浆肾素活性和Ang II水平呈剂量相关升高,在给药第8天比第1天更明显。尽管存在这种代偿机制,但在第1天和第8天,Ang II的时间积分收缩压反应与TCV-116的活性代谢产物CV-11974的时间积分水平之间的关系并无差异。总之,在男性中,TCV-116似乎是一种耐受性良好、口服活性强、效力高且作用持久的Ang II拮抗剂。

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