Dammann H G, Simon B, Müller P, Krüger H J
Arzneimittelforschung. 1982;32(3):309-10.
The effect of 50 and 100 mg of 5,11-dihydro-11-[(4-methyl-piperazin-1-yl)acetyl]-6H-pyrido]2,3-b][1,4]benzodiazepin-6-one dihydrochloride (pirenzepine), respectively, given p.o. at 6 p.m. on nocturnal acid secretion was tested in 6 healthy volunteers. Pirenzepine showed a long-lasting antisecretory activity. The total acid output between 0 a.m. and 6 a.m. was reduced with 50 mg of pirenzepine by about 32% and with 100 mg of pirenzepine by about 41%. It is assumed that pirenzepine (100 mg at bedtime) should be tested in the prevention of relapse in chronic duodenal ulcer disease.
分别给6名健康志愿者口服50毫克和100毫克的5,11 - 二氢 - 11 - [(4 - 甲基 - 哌嗪 - 1 - 基)乙酰基] - 6H - 吡啶并[2,3 - b][1,4]苯并二氮杂䓬 - 6 - 酮二盐酸盐(哌仑西平),测试其对夜间胃酸分泌的影响。哌仑西平显示出持久的抗分泌活性。凌晨0点至6点的总酸分泌量,50毫克哌仑西平使其减少约32%,100毫克哌仑西平使其减少约41%。据推测,应测试哌仑西平(睡前100毫克)对预防慢性十二指肠溃疡疾病复发的效果。