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低剂量法莫替丁、雷尼替丁或安慰剂对人五肽胃泌素刺激胃酸分泌的早期和晚期影响。

Early and late effects of low-dose famotidine, ranitidine or placebo on pentagastrin-stimulated gastric acid secretion in man.

作者信息

Grimley C E, West J M, Loft D E, Cottrell J, Mann S G, Stauffer L, Nwokolo C U

机构信息

Department of Gastroenterology, Walsgrave Hospital, Coventry, UK.

出版信息

Aliment Pharmacol Ther. 1996 Oct;10(5):743-7. doi: 10.1046/j.1365-2036.1996.51193000.x.

Abstract

BACKGROUND

There are no published comparative studies on the effect of low-dose H2-antagonists on pentagastrin-stimulated gastric acid secretion.

METHODS

Twenty-four healthy subjects were dosed with either famotidine 10 mg, ranitidine 75 mg or placebo in a balanced three-period cross-over design. The subjects were studied in groups of 12, simultaneously, under identical controlled environmental conditions. Gastric juice was aspirated in 15-min aliquots during sub-maximal (0.6 microgram.h/kg) intravenous pentagastrin stimulation in the third and fourth hours (early period) and the eighth and ninth hours (late period) after oral dosing. The hydrogen ion (H+) content of gastric juice was measured ex vivo, by titrating to pH7 known volumes of gastric aspirate against 0.1 M sodium hydroxide, using a versatile microprocessor-controlled auto-titration unit. Gastric acid output during the period of interest was calculated by adding the hydrogen ion content of 15-min aliquots collected during that period. The geometric mean of the cumulative pentagastrin-stimulated gastric acid output during the early and late periods was determined for the subjects dosed with either famotidine, ranitidine or placebo. Comparisons were performed by ANOVA.

RESULTS

During the early period (2-4 h post-dose), When the subjects were given placebo, mean gastric acid output was 46.6 mmol, decreasing by 76% to 11.3 mmol (P < 0.001) when treated with famotidine and by 76% to 11.1 mmol (P < 0.001) when treated with ranitidine. During the late period (7-9 h post-dose), when the subjects were dosed with placebo, mean gastric acid output was 41.2 mmol, decreasing by 38% to 25.7 mmol (P < 0.001) when treated with famotidine and by 27% to 30.0 mmol (P = 0.007) when treated with ranitidine. The difference between the inhibitory effects of famotidine and ranitidine on gastric acid output were non-significant during either period.

CONCLUSIONS

Low-dose famotidine and ranitidine, intended for over-the-counter use, inhibit stimulated gastric acid secretion profoundly in the third and fourth hours after an oral dose. Modest effects are still detectable up to 9 h after dosing.

摘要

背景

目前尚无关于低剂量H2拮抗剂对五肽胃泌素刺激胃酸分泌影响的比较性研究发表。

方法

采用平衡的三周期交叉设计,对24名健康受试者分别给予法莫替丁10毫克、雷尼替丁75毫克或安慰剂。受试者12人一组,在相同的受控环境条件下同时进行研究。在口服给药后的第三和第四小时(早期)以及第八和第九小时(晚期),在次最大剂量(0.6微克·小时/千克)静脉注射五肽胃泌素刺激期间,以15分钟的间隔抽取胃液。通过使用通用的微处理器控制自动滴定装置,将已知体积的胃抽吸物用0.1 M氢氧化钠滴定至pH7,离体测量胃液中的氢离子(H+)含量。通过将该时间段内收集的15分钟间隔的氢离子含量相加,计算感兴趣时间段内的胃酸分泌量。确定给予法莫替丁、雷尼替丁或安慰剂的受试者在早期和晚期累积五肽胃泌素刺激胃酸分泌量的几何平均值。采用方差分析进行比较。

结果

在早期(给药后2 - 4小时),给予安慰剂时,平均胃酸分泌量为46.6毫摩尔,用 法莫替丁治疗时降至11.3毫摩尔,下降了76%(P < 0.001),用雷尼替丁治疗时降至11.1毫摩尔,下降了76%(P < 0.001)。在晚期(给药后7 - 9小时),给予安慰剂时,平均胃酸分泌量为41.2毫摩尔,用法莫替丁治疗时降至25.7毫摩尔,下降了38%(P < 0.001),用雷尼替丁治疗时降至30.0毫摩尔,下降了27%(P = 0.007)。在两个时间段内,法莫替丁和雷尼替丁对胃酸分泌抑制作用的差异均无统计学意义。

结论

用于非处方用途的低剂量法莫替丁和雷尼替丁在口服给药后的第三和第四小时可显著抑制刺激后的胃酸分泌。给药后长达9小时仍可检测到适度的作用。

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