Watkins J, Dargie H J, Brown M J, Krikler D M, Dollery C T
Br Heart J. 1982 Jun;47(6):539-45. doi: 10.1136/hrt.47.6.539.
Myocardial histamine(H)2 receptor stimulation has been studied in six normal men. Since histamine is a potent vasodilator, the haemodynamic effects of histamine infusion were compared with those of nitroprusside at equihypotensive doses, to identify changes in myocardial contractility attributable to vasodilatation. After H1 receptor blockade with mepyramine, subjects received, in single blind crossover fashion, either histamine alone and with the H2 receptor antagonist cimetidine, or nitroprusside alone and with cimetidine. Echocardiographic left ventricular dimensions, plasma catecholamines, blood pressure, and heart rate were measured. The rise in catecholamines suggested similar baroreflex activation by both histamine and nitroprusside. Echo ejection phase indices did not alter significantly after nitroprusside, but histamine caused an increase in percentage fractional shortening from 38.2 +/- 4.1 to 53.5 +/- 3-6% and in mean fibre shortening velocity from 1.31 +/- 0.19 to 1.99 +/- 0.22 cm/s. These changes were both greatly reduced by cimetidine and suggest that H2 receptor stimulation in man causes a direct positive inotropic response.
对6名正常男性的心肌组胺(H)2受体刺激情况进行了研究。由于组胺是一种强效血管扩张剂,因此在等降压剂量下,将组胺输注的血流动力学效应与硝普钠的效应进行比较,以确定血管扩张引起的心肌收缩力变化。在用美吡拉敏阻断H1受体后,受试者以单盲交叉方式接受单独使用组胺以及联合使用H2受体拮抗剂西咪替丁,或者单独使用硝普钠以及联合使用西咪替丁的处理。测量了超声心动图左心室尺寸、血浆儿茶酚胺、血压和心率。儿茶酚胺的升高表明组胺和硝普钠对压力感受器反射的激活作用相似。硝普钠给药后,回声射血期指标无明显变化,但组胺使缩短分数百分比从38.2±4.1%增加到53.5±3.6%,平均纤维缩短速度从1.31±0.19 cm/s增加到1.99±0.22 cm/s。西咪替丁可大大减轻这些变化,提示人体中的H2受体刺激可引起直接的正性肌力反应。