Chan P S, Ronsberg M A, Cervoni P
Clin Exp Hypertens A. 1982;4(6):1019-34. doi: 10.3109/10641968209060769.
In spontaneously hypertensive rats (SHR), captopril at 30 and hydrochlorothiazide (HCTZ) at 100 mg/kg/day p.o. for 2 days lowered mean arterial blood pressure (MABP) 16 and 10 mm Hg, respectively. Treatment with the combination of captopril plus HCTZ for one day lowered MABP to the same extent as captopril alone, but produced a synergistic 44 mm Hg MABP lowering after the second day combination treatment. Bilateral ureteral ligation did not prevent the synergistic antihypertensive effect demonstrating that removal of electrolytes was not the cause of this effect. Cardiovascular responses to angiotensin-I and -II, norepinephrine or bradykinin did not differ in rats given the combination or captopril alone. After the combination treatment for one day, captopril but not HCTZ alone on the second day lowered MABP in rats to the same degree as in those receiving the combination treatment for 2 days, suggesting that the diuretic action per se is unimportant. Captopril and HCTZ increased plasma renin activity (PRA) but only the combination of captopril and HCTZ produced a greater and longer lasting increase of PRA. It is concluded that the mechanism for the synergism is the renin dependency, created by the combination of HCTZ and captopril, resulting in a greater role of the renin system in blood pressure control and increased responsiveness to angiotensin converting enzyme inhibition by captopril.
在自发性高血压大鼠(SHR)中,口服卡托普利30mg/kg/天和氢氯噻嗪(HCTZ)100mg/kg/天,持续2天,平均动脉血压(MABP)分别降低了16mmHg和10mmHg。卡托普利加HCTZ联合治疗1天,MABP降低程度与单独使用卡托普利相同,但在联合治疗第2天后,产生了协同作用,使MABP降低了44mmHg。双侧输尿管结扎并未阻止这种协同降压作用,表明电解质清除不是这种作用的原因。联合用药组大鼠与单独给予卡托普利组大鼠相比,对血管紧张素-I和-II、去甲肾上腺素或缓激肽的心血管反应并无差异。联合治疗1天后,单独给予卡托普利而非HCTZ,在第2天将大鼠的MABP降低到与联合治疗2天的大鼠相同程度,这表明利尿剂本身的作用并不重要。卡托普利和HCTZ均可增加血浆肾素活性(PRA),但只有卡托普利与HCTZ联合使用时,才会使PRA出现更大且更持久的升高。得出的结论是,协同作用的机制是HCTZ和卡托普利联合产生的肾素依赖性,导致肾素系统在血压控制中发挥更大作用,并增强了对卡托普利抑制血管紧张素转换酶的反应性。