[阿托品和甲氧氯普胺对健康先试者萨拉唑磺吡啶口服转运时间的影响]。

B Terhaag, A Neugebauer
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引用次数: 0

摘要

对9名健康男性志愿者首次出现的磺胺吡啶进行了调查。在三路交叉设计中,单独给予6 g萨拉唑吡林,与甲氧氯普胺(0.3 mg/kg i.m)或阿托品(0.01 mg/kg i.m)。在对照组中,磺胺吡啶在(平均值+/- S平均值)6.2 h +/- 0.8 h(范围:3-11 h)出现在血液中。甲氧氯普胺首次出现时间为3.6 h +/- 0.7 h(范围:2-8 h),阿托品首次出现时间为8.1 h +/- 0.8 h(范围:6-12 h), p < 0.05,差异有统计学意义。结果显示在胃肠道运动的药理学修饰,因此有用的萨拉唑吡啶来确定运输时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Modification of orocecal transit time of salazosulfapyridine by atropine and metoclopramide in healthy probands].

The first appearance of sulpharyridine in plasma was investigated in nine healthy informed male volunteers. In a three way crossover design 6 g salazopyrin alone, together with metoclopramide (0.3 mg/kg i.m.) or atropine (0.01 mg/kg i.m.) were given. Sulphapyridine appears in the blood at the (means +/- S means) 6.2 h +/- 0.8 h (range: 3-11 h) in controls. Together with metoclopramide the first appearance is 3.6 h +/- 0.7 h (range: 2-8 h) and together with atropine these values are 8.1 +/- 0.8 h (range: 6-12 h). The differences are significant with p less than 0.05. The results show the pharmacological modification of motility in the gastrointestinal tract and in consequence the usefulness of salazopyridine to determine the transit time.

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