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用治疗剂量的西咪替丁或新型组胺H2受体拮抗剂雷米替丁(CM 57755A)对人类志愿者进行为期2周治疗后其血浆催乳素、性激素和胃泌素的情况

Plasma prolactin, sex steroids and gastrin in human volunteers treated for 2 weeks with therapeutic doses of cimetidine or the new histamine H2-receptor antagonist ramixotidine (CM 57755A).

作者信息

Colle M, Ruedas E, Cazenave J, Auzerie J, Basilisco G, Camboni G, Manara L

机构信息

Institut Robert Greenblatt, Bordeaux, France.

出版信息

Eur J Clin Pharmacol. 1988;35(5):529-34. doi: 10.1007/BF00558249.

Abstract

Three groups of eight healthy male volunteers received placebo for 2 days, then daily morning doses either of cimetidine 800 mg, ramixotidine 750 mg (CM 57755A), or placebo, for 14 days, and then were all returned to placebo for one more day. Plasma levels of prolactin, testosterone and 17 beta-estradiol were measured on Days 2, 3, 16 and 17 in blood samples taken 30 and 15 min before and 0, 60, 120, 180, 240 and 300 min after treatment. Gastrin was assayed in blood collected on the same days 180 min after treatment. Mean pre- and post-treatment areas under the time-concentration curves of the first three hormones were not significantly different in the three groups on any test day, or within the same group throughout the four test days. Mean plasma gastrin levels ranged between 27 and 42 pg/ml, respectively, in the placebo and cimetidine treated groups on test day 3, and intermediate values were found in the group receiving CM 57755A. There was no statistically significant difference in gastrin level between the groups on any test day or within the same group throughout the four test days. No subjective side-effects attributable to the treatments were reported, and there were no abnormalities in blood pressure, heart rate or standard laboratory tests.

摘要

三组,每组八名健康男性志愿者,先服用2天安慰剂,然后连续14天每天早晨分别服用800毫克西咪替丁、750毫克雷米替丁(CM 57755A)或安慰剂,之后再服用1天安慰剂。在治疗前30分钟和15分钟以及治疗后0、60、120、180、240和300分钟采集血样,分别在第2、3、16和17天测量血浆催乳素、睾酮和17β-雌二醇水平。在治疗后180分钟采集的同一天血液中检测胃泌素。在任何测试日,三组中前三种激素的治疗前和治疗后时间-浓度曲线下面积均值无显著差异,且在整个四个测试日内同一组内也无显著差异。在测试日3,安慰剂组和西咪替丁治疗组的血浆胃泌素水平均值分别在27至42皮克/毫升之间,接受CM 57755A的组中值介于两者之间。在任何测试日,三组间胃泌素水平无统计学显著差异,且在整个四个测试日内同一组内也无显著差异。未报告与治疗相关的主观副作用,血压、心率或标准实验室检查均无异常。

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