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雷尼替丁服用12 - 13小时后对进食的胃分泌反应。

Gastric secretion in response to a meal 12-13 h after ranitidine.

作者信息

Frislid K, Berstad A

出版信息

Scand J Gastroenterol. 1985 Aug;20(6):711-4. doi: 10.3109/00365528509089200.

Abstract

In a recent study we demonstrated a marked inhibition of basal gastric acid secretion 12-14 h after oral administration of 150 mg ranitidine. This study investigates the effect of ranitidine on meal-evoked secretion, time interval between drug administration and measurements remaining the same as in a former study. Under the present conditions 150 mg ranitidine had no effect on acid secretion and enhanced pepsin secretion. The results indicate that the effect of the H2-receptor antagonist is surmountable by meal stimulation. The concentrations of ranitidine in basal gastric juice was approximately the same as in blood. The gastric excretion of ranitidine did not increase by meal stimulation and was approximately 0.5% of the excretion in urine.

摘要

在最近的一项研究中,我们证明口服150毫克雷尼替丁12 - 14小时后,基础胃酸分泌受到显著抑制。本研究调查雷尼替丁对进餐诱发分泌的影响,给药与测量之间的时间间隔与之前的研究相同。在目前的条件下,150毫克雷尼替丁对胃酸分泌没有影响,但增强了胃蛋白酶分泌。结果表明,H2受体拮抗剂的作用可被进餐刺激克服。基础胃液中雷尼替丁的浓度与血液中的大致相同。进餐刺激并未增加雷尼替丁的胃排泄量,其胃排泄量约为尿排泄量的0.5%。

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