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一种评估药物诱发小鼠胃排空变化的改良方法。

An improved method of evaluation of drug-evoked changes in gastric emptying in mice.

作者信息

Osinski M A, Seifert T R, Cox B F, Gintant G A

机构信息

Department of Integrative Pharmacology, R46R AP9-1, Abbott Laboratories, 100 Abbott Park Road, Abbott Park, IL 60064-6119, USA.

出版信息

J Pharmacol Toxicol Methods. 2002 Mar-Apr;47(2):115-20. doi: 10.1016/s1056-8719(02)00217-4.

Abstract

INTRODUCTION

The increased availability of transgenic mice prompts a need for the adaptation to mice of whole-animal assays traditionally performed in larger laboratory animals. Gastric emptying studies are frequently conducted in dogs and rats. Mouse-based gastric emptying models currently available often use inert, nonnutrient liquid meals containing nonabsorbable markers or radionuclides. We have developed a mouse gastric emptying assay that features a favorable throughput and the use of a semisolid, high-calorie meal.

METHODS

A carbohydrate- and protein-rich semisolid test meal was prepared from common laboratory reagents. Gastric emptying was determined by subtracting the mass of test meal remaining in the stomach from the mass of test meal administered. A time-course study of basal emptying of a semisolid, paste-like test meal high in carbohydrate and protein from the stomachs of overnight-fasted mice was conducted. Agents known to either inhibit (propantheline, 0.3-10 mg/kg sc; corticotropin-releasing factor [CRF], 3-100 nmol/kg ip) or accelerate (metoclopramide, 1-10 mg/kg ip; bethanechol, 1-30 mg/kg ip) gastric emptying were tested. A single time-point variation of the assay can be used for quickly screening compounds for effects on gastric emptying.

RESULTS

In time-course studies, the test meal emptied from the stomach with a half-emptying time of 30.6 min (95% CI: 27.3-34.7). The gastric emptying data were successfully modeled by a two-parameter exponential decay function. No lag phase was observed, indicating that the meal empties from the stomach as a liquid. The anticholinergic agent propantheline increased gastric half-emptying time (t(1/2)) approximately threefold, while metoclopramide decreased gastric half-emptying time approximately twofold compared to basal emptying. Single time-point screening studies correctly detected the gastrokinetic activity of bethanechol and the inhibitory effect of CRF.

DISCUSSION

The mouse gastric emptying assay reported here is simple, inexpensive, and not labor-intensive. It is capable of detecting either stimulation or inhibition of gastric motor activity. This assay should prove useful for identifying drug-evoked changes in gastric emptying as well as for assessing the gastric motility effects of altered gene expression in genetically modified mice.

摘要

引言

转基因小鼠的可得性增加,促使人们需要将传统上在较大实验动物中进行的全动物试验方法应用于小鼠。胃排空研究经常在狗和大鼠中进行。目前可用的基于小鼠的胃排空模型通常使用含有不可吸收标记物或放射性核素的惰性、无营养液体餐。我们开发了一种小鼠胃排空试验,该试验具有良好的通量,并使用半固体、高热量餐。

方法

由常见实验室试剂制备富含碳水化合物和蛋白质的半固体试验餐。通过从给予的试验餐质量中减去胃中剩余的试验餐质量来确定胃排空。对过夜禁食小鼠胃中富含碳水化合物和蛋白质的半固体、糊状试验餐的基础排空进行了时间进程研究。测试了已知可抑制(溴丙胺太林,0.3 - 10毫克/千克皮下注射;促肾上腺皮质激素释放因子[CRF],3 - 100纳摩尔/千克腹腔注射)或加速(胃复安,1 - 10毫克/千克腹腔注射;氨甲酰甲胆碱,1 - 30毫克/千克腹腔注射)胃排空的药物。该试验的单个时间点变化可用于快速筛选化合物对胃排空的影响。

结果

在时间进程研究中,试验餐从胃中排空,半排空时间为30.6分钟(95%置信区间:27.3 - 34.7)。胃排空数据成功地用双参数指数衰减函数建模。未观察到延迟期,表明餐食以液体形式从胃中排空。抗胆碱能药物溴丙胺太林使胃半排空时间(t(1/2))增加约三倍,而胃复安与基础排空相比使胃半排空时间减少约两倍。单个时间点筛选研究正确地检测到了氨甲酰甲胆碱的胃肠动力活性和CRF的抑制作用。

讨论

本文报道的小鼠胃排空试验简单、廉价且不耗费大量人力。它能够检测胃运动活性的刺激或抑制。该试验对于识别药物引起的胃排空变化以及评估转基因小鼠基因表达改变对胃动力的影响应该是有用的。

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