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在正常血压受试者中,TCV - 116对血管紧张素II的升压和醛固酮反应的持续抑制作用。

Persistent inhibition of the pressor and aldosterone responses to angiotensin-II by TCV-116 in normotensive subjects.

作者信息

Ogihara T, Nagano M, Higaki J, Kohara K, Mikami H

机构信息

Department of Geriatric Medicine, Osaka University Medical School, Suita, Japan.

出版信息

J Cardiovasc Pharmacol. 1995 Sep;26(3):490-4. doi: 10.1097/00005344-199509000-00021.

Abstract

TCV-116 is an orally active, nonpeptide antagonist of angiotensin-II type-1 receptor. The angiotensin-II antagonistic potency of TCV-116 was evaluated in normal volunteers. TCV-116 was administered at single doses of 1, 2.5, and 5 mg orally on separated days. Before, and 4, 8, and 24 h after the drug administration, angiotensin-II was infused intravenously at the rate of 2.5 to 40 ng/kg/min for 5 min each. At 2.5 mg of TCV-116, the pressor response to angiotensin-II was significantly suppressed at 4 and 8 hours after drug administration. TCV-116 at 5 mg produced a reduction of basal blood pressure and a suppression of pressor response to angiotensin-II, which persisted for 24 h. Aldosterone response to exogenous angiotensin-II was suppressed to 10% at 8 h after 5 mg of TCV-116 administration and remained suppressed to 48% until 24 h. These results suggest that TCV-116 is a highly potent and long-lasting antagonist of angiotensin-II receptor in man. The renin-angiotensin system may play a role in the regulation of blood pressure even in normotensive subjects.

摘要

TCV-116是一种口服有效的血管紧张素II 1型受体非肽拮抗剂。在正常志愿者中评估了TCV-116的血管紧张素II拮抗效力。在不同日期分别口服给予TCV-116单剂量1、2.5和5毫克。在给药前以及给药后4、8和24小时,以2.5至40纳克/千克/分钟的速率静脉输注血管紧张素II,每次输注5分钟。给予2.5毫克TCV-116后,给药后4小时和8小时对血管紧张素II的升压反应被显著抑制。5毫克的TCV-116使基础血压降低,并抑制了对血管紧张素II的升压反应,这种作用持续24小时。给予5毫克TCV-116后8小时,对外源性血管紧张素II的醛固酮反应被抑制至10%,并持续抑制至24小时,抑制率为48%。这些结果表明,TCV-116是人体中一种高效且长效的血管紧张素II受体拮抗剂。肾素-血管紧张素系统可能在血压调节中发挥作用,即使在血压正常的受试者中也是如此。

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