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口服血管紧张素转换酶(ACE)抑制剂后大鼠的降压活性与小鼠血浆血管紧张素转换酶(ACE)抑制之间的相关性。

Correlation between anti-hypertensive activity in rats and plasma angiotensin I-converting enzyme (ACE) inhibition in mice following oral administration of ACE inhibitors.

作者信息

Pong S F, Brooks R R, Huang C T, Moore A F

出版信息

Pharmacol Res Commun. 1985 Apr;17(4):331-44. doi: 10.1016/0031-6989(85)90013-x.

DOI:10.1016/0031-6989(85)90013-x
PMID:2989953
Abstract

Thirty-four ACE inhibitors were evaluated to determine the concentration giving 50% inhibition of purified rabbit lung ACE (IC50 microM) using benzyloxycarboxyl-p-NO2-Phe-His-Leu as substrate, to determine the oral dose causing a lowering in blood pressure of 30 mm Hg (ED30 mumol/kg) in acute aortic coarctate (AAC) rats, and to determine inhibition of plasma ACE (PACE) activity in mice after oral dosing. Mouse PACE activity was determined with 14C-Hip-His-Leu as substrate one hour after oral dosing of 3 animals/group with 5 or 50 mumol ACE inhibitor per kg. Data from mice were expressed as percent of control group PACE activity. Least squares regression analysis showed the IC50 data to be poorly correlated with either rat data or mouse PACE data at 50 mumol/kg p.o. However, correlation was significant between log rat ED30 and mouse PACE at 5 (p less than 0.001, r = 0.570) and 50 (p less than 0.025, r = 0.387) mumol/kg p.o. Thus, the simple mouse plasma ACE determination after a dose of 5 mumol/kg is a convenient supplement to the AAC rat model for showing oral activity of ACE inhibitors.

摘要

使用苄氧基羰基 - 对硝基苯丙氨酸 - 组氨酸 - 亮氨酸作为底物,对34种血管紧张素转换酶(ACE)抑制剂进行评估,以确定对纯化的兔肺ACE产生50%抑制作用时的浓度(IC50,微摩尔);确定在急性主动脉缩窄(AAC)大鼠中使血压降低30 mmHg时的口服剂量(ED30,微摩尔/千克);并确定口服给药后小鼠血浆ACE(PACE)活性的抑制情况。在每组3只动物口服每千克5或50微摩尔ACE抑制剂1小时后,以14C - 马尿酰 - 组氨酸 - 亮氨酸作为底物测定小鼠的PACE活性。小鼠的数据表示为对照组PACE活性的百分比。最小二乘法回归分析表明,在口服50微摩尔/千克时,IC50数据与大鼠数据或小鼠PACE数据的相关性较差。然而,在口服5(p小于0.001,r = 0.570)和50(p小于0.025,r = 0.387)微摩尔/千克时,大鼠ED30的对数与小鼠PACE之间的相关性显著。因此,在给予5微摩尔/千克剂量后简单测定小鼠血浆ACE是对AAC大鼠模型的一种方便补充,用于显示ACE抑制剂的口服活性。

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