Levander S, Hägermark O, Ståhle M
Eur J Clin Pharmacol. 1985;28(5):523-9. doi: 10.1007/BF00544062.
The effects of single oral doses of three antihistamine compounds on histamine-induced itch and flare reactions were studied in 24 healthy volunteers by a double-blind balanced design. Central sedative effects were concurrently analyzed using a set of computerized neuropsychological tests and analogue ratings. Hydroxyzine 20 mg had a more pronounced inhibitory effect on the cutaneous response than 3 mg clemastine or 3 mg azatadine. Clemastine tended to cause more sedation than the other two drugs. A compound score, reflecting the balance between peripheral and CNS effects, showed hydroxyzine to have relatively more peripheral antihistamine effect and less sedative effect than the other two drugs. The independence of peripheral and CNS antihistamine effects was also suggested by correlation analysis. Subjects displayed individual sensitivity to the peripheral antihistamine effect of the three drugs; a marked antihistamine effect of one drug predicted a marked effect of the other two drugs. This was not the case for CNS sedation. The independence of peripheral and CNS effects should encourage development of new and more specific antihistamine compounds.
采用双盲均衡设计,在24名健康志愿者中研究了单次口服三种抗组胺化合物对组胺诱发的瘙痒和潮红反应的影响。同时使用一组计算机化神经心理学测试和类比评分来分析中枢镇静作用。20毫克羟嗪对皮肤反应的抑制作用比3毫克氯马斯汀或3毫克阿扎他定更明显。氯马斯汀比其他两种药物更容易引起镇静作用。一个反映外周和中枢神经系统作用平衡的复合评分显示,与其他两种药物相比,羟嗪具有相对更强的外周抗组胺作用和较弱的镇静作用。相关性分析也表明外周和中枢神经系统抗组胺作用具有独立性。受试者对这三种药物的外周抗组胺作用表现出个体敏感性;一种药物的显著抗组胺作用预示着其他两种药物也会有显著作用。中枢神经系统镇静作用并非如此。外周和中枢神经系统作用的独立性应会促进新型、更具特异性的抗组胺化合物的研发。