Brown C L, Backhouse C I, Grippat J C, Santoni J P
Servier Research and Development, Fulmer, Bucks., UK.
Eur J Clin Pharmacol. 1990;39(4):327-32. doi: 10.1007/BF00315404.
The pharmacodynamic effects and acceptability of perindopril (4 mg daily) and hydrochlorothiazide (25 mg daily) given alone or in combination for 1 month were investigated in a double-blind, placebo controlled, parallel group study. The pharmacokinetics of perindopril and its active metabolite perindoprilat and the time course of angiotensin converting enzyme inhibition were studied for 72 h following the last dose of treatment in the two appropriate groups. Similar decreases in blood pressure were seen 24 h after the last dose of perindopril or hydrochlorothiazide (11/7 mm Hg supine) given alone at these doses. The effect of these drugs given together was additive on diastolic blood pressure and synergistic on systolic blood pressure (24.5/12.6 mm Hg supine) taking into account the placebo response. The significant increase in plasma renin activity produced by perindopril alone was potentiated by concurrent administration of hydrochlorothiazide. The formation of perindoprilat was slightly reduced in the group also receiving hydrochlorothiazide and there was a very small reduction in ACE inhibition in this group. Perindopril, whether given alone or in combination with hydrochlorothiazide, was well tolerated and produced no clinically significant change in routine haematology or serum biochemistry. The additive or synergistic effects of perindopril and hydrochlorothiazide on blood pressure must be due to their complementary physiological actions and not to a pharmacokinetic interaction.
在一项双盲、安慰剂对照、平行组研究中,对单独或联合使用培哚普利(每日4毫克)和氢氯噻嗪(每日25毫克)治疗1个月的药效学作用和可接受性进行了研究。在两个合适的组中,于最后一剂治疗后72小时研究了培哚普利及其活性代谢物培哚普利拉的药代动力学以及血管紧张素转换酶抑制的时间过程。在这些剂量下单独给予最后一剂培哚普利或氢氯噻嗪后24小时,观察到血压有类似程度的下降(仰卧位时下降11/7毫米汞柱)。考虑到安慰剂反应,这些药物联合使用对舒张压的作用是相加的,对收缩压的作用是协同的(仰卧位时下降24.5/12.6毫米汞柱)。单独使用培哚普利引起的血浆肾素活性显著增加,因同时给予氢氯噻嗪而增强。在同时接受氢氯噻嗪的组中,培哚普利拉的形成略有减少,且该组中血管紧张素转换酶抑制作用有非常小的降低。培哚普利无论单独使用还是与氢氯噻嗪联合使用,耐受性均良好,且在常规血液学或血清生物化学方面未产生临床上显著的变化。培哚普利和氢氯噻嗪对血压的相加或协同作用必定归因于它们互补的生理作用,而非药代动力学相互作用。