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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对胃肠系统中推进(转运)时间的影响。这项研究旨在比较临床上已知对大鼠和小鼠的通便时间有影响的三种化合物,它们会引起便秘(硫酸吗啡和溴化丙氨茶碱)和泻药(盐酸甲氧氯普胺),并说明两者之间是否存在差异。方法:将化合物在清醒的大鼠和小鼠中给药。在给药后0.5-2.0h(估计每种化合物的最大血浆浓度的时间),用适当体积(基于重量)的10%活性粉末状碳悬浮在5%阿拉伯树胶中给动物灌胃。给药后四十五分钟,通过CO 2窒息处死动物,并除去小肠。相对于肠段的总长度测量木炭前缘的位置。结果:测试的化合物在物种之间的传播时间上产生了可变的统计差异。在两个啮齿动物模型中,吗啡和propantheline产生的转运时间呈剂量依赖性增加,而甲氧氯普胺减少了转运时间,在统计学上显着。讨论:本数据表明,在相似剂量下,大鼠和小鼠可互换用于转运研究。在较高剂量的测试化合物下,小鼠对转运变化更敏感。

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