Feldman M, Richardson C T
Adv Intern Med. 1978;23:1-24.
Development of histamine H2-receptor antagonists has enhanced the understanding of histamine physiology and pharmacology. The effect of H2-receptor antagonists on gastrointestinal physiology has been studied extensively. These compounds inhibit gastric acid secretion in response to all known secretagogues and, in contrast to anticholinergic drugs, markedly inhibit food-stimulated acid secretion in duodenal ulcer patients. The relative roles of H2-receptor antagonists, anticholinergic drugs and antacids in the treatment of duodenal ulcer remain to be defined. Cimetidine currently is under investigation for the treatment of duodenal ulcer, gastric ulcer, reflux esophagitis, gastrointestinal bleeding and hypersecretory states. Although the long-term safety of cimetidine has not been established, in short-term clinical trials there have been no significant subjective or objective side-effects. Assuming that toxic effects do not develop, H2-receptor antagonists should improve the treatment of acid-peptic disease.
组胺H2受体拮抗剂的研发增进了人们对组胺生理学和药理学的理解。H2受体拮抗剂对胃肠生理学的影响已得到广泛研究。这些化合物能抑制对所有已知促分泌剂产生反应的胃酸分泌,并且与抗胆碱能药物不同,能显著抑制十二指肠溃疡患者食物刺激引起的胃酸分泌。H2受体拮抗剂、抗胆碱能药物和抗酸剂在十二指肠溃疡治疗中的相对作用仍有待确定。西咪替丁目前正在进行治疗十二指肠溃疡、胃溃疡、反流性食管炎、胃肠道出血和分泌过多状态的研究。尽管西咪替丁的长期安全性尚未确立,但在短期临床试验中未出现明显的主观或客观副作用。假设不会产生毒性作用,H2受体拮抗剂应能改善酸相关性疾病的治疗。