Antonaccio M J, Rubin B, Horovitz Z P, Laffan R J, Goldberg M E, High J P, Harris D N, Zaidi I
Jpn J Pharmacol. 1979 Apr;29(2):285-94. doi: 10.1254/jjp.29.285.
The effects of hydralazine (3 mg/kg) and the angiotensin I-converting enzyme (ACE) inhibitor captopril (SQ 14,225) (100 mg/kg) on mean arterial blood pressure, plasma renin activity, urinary volume and urinary Na+,K+, and aldosterone concentrations were examined in spontaneously hypertensive rats of the Okamoto and Aoki strain (SHR) after oral daily dosing for 2 weeks, 3 or 6 months. Captopril caused progressive cumulative reductions in blood pressure resulting in normalization of pressure after 6 months of dosing. Hydralazine also significantly reduced blood pressure but not to the level of normotensive rats of the Wistar-Kyoto strain (WKY). Reductions in heart size paralleled the changes in blood pressure, normalization of cardiac hypertrophy occurring after captopril but not hydralazine. Plasma renin activity increased approximately 2-3 fold after hydralazine and 15-fold after captopril. Neither hydralazine nor captopril had any consistent effects on 24-hr urine volume, urinary Na+,K+ or aldosterone excretion. These results indicate that chronic inhibition of ACE with captopril induces normalization of blood pressure in SHR, a normal-renin model of hypertension.
在冈本和青木品系的自发性高血压大鼠(SHR)中,每日经口给药2周、3个月或6个月后,检测了肼屈嗪(3毫克/千克)和血管紧张素I转换酶(ACE)抑制剂卡托普利(SQ 14,225)(100毫克/千克)对平均动脉血压、血浆肾素活性、尿量以及尿钠、钾和醛固酮浓度的影响。卡托普利使血压逐渐累积下降,给药6个月后血压恢复正常。肼屈嗪也显著降低了血压,但未降至Wistar-Kyoto品系(WKY)正常血压大鼠的水平。心脏大小的缩小与血压变化平行,卡托普利给药后心脏肥大恢复正常,而肼屈嗪则未使其恢复正常。肼屈嗪给药后血浆肾素活性增加约2 - 3倍,卡托普利给药后增加15倍。肼屈嗪和卡托普利对24小时尿量、尿钠、钾或醛固酮排泄均无一致的影响。这些结果表明,用卡托普利长期抑制ACE可使SHR(一种正常肾素型高血压模型)的血压恢复正常。