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奥美拉唑可抑制人体夜间及五肽胃泌素刺激的胃酸分泌。

Omeprazole inhibits nocturnal and pentagastrin-stimulated gastric secretion in man.

作者信息

Wilson J A, Boyd E J, Wormsley K G

出版信息

Dig Dis Sci. 1984 Sep;29(9):797-801. doi: 10.1007/BF01318421.

Abstract

The effect of omeprazole on the overnight and pentagastrin-stimulated gastric secretion of acid and pepsin have been studied in healthy male volunteers. After treatment with omeprazole, 30 mg or 60 mg daily for one week, overnight secretion of acid was reduced by 48 and 73%, respectively. During stimulation with pentagastrin, a single dose of 40 mg omeprazole reduced acid output by 98%, while after 80 mg, secretion of acid and pepsin was completely abolished. Omeprazole is one of the most potent gastric secretory inhibitors available at present, with potential for use in the therapy of ulcer disease.

摘要

在健康男性志愿者中研究了奥美拉唑对夜间及五肽胃泌素刺激的胃酸和胃蛋白酶分泌的影响。用奥美拉唑每日30毫克或60毫克治疗一周后,夜间胃酸分泌分别减少了48%和73%。在用五肽胃泌素刺激期间,单剂量40毫克奥美拉唑使胃酸分泌量减少了98%,而80毫克后,胃酸和胃蛋白酶的分泌完全被抑制。奥美拉唑是目前可用的最有效的胃分泌抑制剂之一,有用于溃疡病治疗的潜力。

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