Molinder H K
Department of Family Medicine, University of Uppsala, Sweden.
J Clin Gastroenterol. 1994 Oct;19(3):248-54. doi: 10.1097/00004836-199410000-00017.
There was still controversy regarding the physiology of acid secretion in 1964 when a team at Smith Kline & French Laboratories in England started a project to prove the existence of more than one receptor for histamine and to find a substance capable of blocking the effects not blocked by the commonly used antihistamines. The team was convinced that histamine was the final mediator of acid secretion. After 8 years, James Black and his coworkers published evidence of the first histamine2-receptor antagonist, burimamide. As this substance was not suitable for oral therapy, the research continued. Metiamide was synthesized with promising clinical effects but questionable safety. The final answer was cimetidine (Tagamet), approved in England in November 1976. Cimetidine was a breakthrough in the treatment of peptic ulcers. In this article I focus on the human factors lying behind many of the decisions made during the years of research. Without personal courage under stressful conditions, the H2-receptor antagonists might never have reached the market.
1964年,当英国史克必成实验室的一个团队启动一个项目,以证明组胺存在不止一种受体,并寻找一种能够阻断常用抗组胺药无法阻断的效应的物质时,关于胃酸分泌生理学仍存在争议。该团队确信组胺是胃酸分泌的最终介质。8年后,詹姆斯·布莱克和他的同事发表了首个组胺2受体拮抗剂——布立马胺的证据。由于这种物质不适合口服治疗,研究继续进行。甲硫米特被合成出来,具有有前景的临床效果,但安全性存疑。最终的答案是西咪替丁(泰胃美),于1976年11月在英国获批。西咪替丁是消化性溃疡治疗方面的一项突破。在本文中,我关注多年研究过程中许多决策背后的人为因素。如果没有在压力条件下的个人勇气,H2受体拮抗剂可能永远无法推向市场。