Parker J D, Parker A B, Farrell B, Parker J O
Division of Cardiology, University of Toronto, Mount Sinai Hospital, Ontario, Canada.
J Pharmacol Exp Ther. 1997 Feb;280(2):866-75.
It has been reported that nitroglycerin (GTN) tolerance can be prevented by the concurrent administration of hydralazine. Although the mechanism of this effect remains unknown, it is possible that hydralazine modifies counter-regulatory responses to nitrate administration. To address this question, we examined the impact of hydralazine therapy on the development of tolerance during sustained therapy with GTN. Twenty normal volunteers and 18 patients with chronic heart failure (mean ejection fraction 30 +/- 2%) were treated for 1 week with hydralazine or placebo in a randomized double-blind fashion. Hydralazine therapy (or placebo) was continued, and subjects then received continuous transdermal GTN for 5 to 7 days. On the first and last day of transdermal GTN therapy, standing HR, systolic blood pressure and hematocrit responses were assessed. HR and blood pressure responses to sublingual GTN (0.6 mg) were also evaluated before and during sustained transdermal GTN therapy. Significant loss of the hemodynamic effects of transdermal GTN occurred during sustained therapy in both the normal volunteer and heart failure groups. Hydralazine had no effect on the development of tolerance to the hemodynamic effect of GTN in either group. In both, transdermal GTN therapy was associated with a significant fall in hematocrit that persisted for the entire treatment period. Hydralazine had no effect on this response. These data suggest that hydralazine therapy does not prevent loss of systemic arterial effects or prevent plasma volume expansion during sustained transdermal GTN therapy.
据报道,同时给予肼屈嗪可预防硝酸甘油(GTN)耐受性。尽管这种效应的机制尚不清楚,但肼屈嗪有可能改变对硝酸盐给药的反调节反应。为了解决这个问题,我们研究了肼屈嗪治疗对GTN持续治疗期间耐受性发展的影响。20名正常志愿者和18名慢性心力衰竭患者(平均射血分数30±2%)以随机双盲方式接受肼屈嗪或安慰剂治疗1周。继续进行肼屈嗪治疗(或安慰剂治疗),然后受试者接受持续经皮GTN治疗5至7天。在经皮GTN治疗的第一天和最后一天,评估站立时的心率、收缩压和血细胞比容反应。在持续经皮GTN治疗之前和期间,还评估了对舌下GTN(0.6mg)的心率和血压反应。在正常志愿者和心力衰竭组的持续治疗期间,经皮GTN的血流动力学效应均出现显著丧失。肼屈嗪对两组中GTN血流动力学效应耐受性的发展均无影响。在两组中,经皮GTN治疗均与整个治疗期间持续存在的血细胞比容显著下降有关。肼屈嗪对此反应无影响。这些数据表明,在持续经皮GTN治疗期间,肼屈嗪治疗不能预防全身动脉效应的丧失或预防血浆容量扩张。