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Pharmacological comparison of peristaltic effects in rats and mice

机译:大鼠和小鼠蠕动作用的药理比较

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Introduction: Conscious rodent models are commonly used to assess the effects of new chemical entities on propulsion (transit) time in the gastrointestinal system. This study was designed to compare three compounds clinically known to cause constipative (morphine sulfate and propantheline bromide) and laxative (metoclopramide hydrochloride) effects on transit time in rats and mice and to note if there are differences between the species. Methods: Compounds were dosed in conscious rats and mice. At 0.5-2.0h post dosing (estimated time to maximal plasma concentration of each compound) animals were gavaged with an appropriate volume (based on weight) of 10% activated powdered carbon suspended in 5% gum arabic. Forty-five minutes following dosing the animals were sacrificed by CO2 asphyxiation and the small intestine was removed. The position of the leading edge of the charcoal was measured relative to the total length of the intestinal segment. Results: The compounds tested produced variable statistical differences in transit time between species. Morphine and propantheline produced dose-dependent increases in transit time, and metoclopramide decreased transit time, statistically significant in both rodent models. Discussion: The present data demonstrate that at similar doses rats and mice can be used interchangeably for transit studies. Mice were more sensitive to transit changes at higher doses of the compounds tested.
机译:简介:有意识的啮齿动物模型通常用于评估新化学实体在胃肠系统中的推进(过渡)时间的影响。本研究旨在比较临床上已知的三种化合物,以引起大鼠和小鼠中的过渡时间和泻药(Metoclaminaide盐酸盐)和泻药(MetoclaminaMide盐酸盐)的影响,并且如果物种之间存在差异,则注意。方法:在有意识的大鼠和小鼠中给药化合物。在0.5-2.0H后剂量(估计时间到每种化合物的最大血浆浓度),动物的适当体积(基于重量)10%活化粉状碳悬浮在5%的阿拉伯语中。用CO 2窒息治疗动物后45分钟,除去小肠。炭的前缘的位置相对于肠道段的总长度测量。结果:该化合物在物种之间的运输时间中产生了可变统计差异。吗啡和预丙基产生过载时间的剂量依赖性,并且甲氯普胺减少过渡时间,啮齿动物模型中的统计学意义。讨论:本数据表明,在类似的剂量中,大鼠和小鼠可以互换用于过境研究。小鼠对经过较高剂量的化合物进行较高剂量的转动变化更敏感。

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