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向大鼠脑室内注射蛙皮素后,其可刺激小肠蠕动。

Bombesin stimulates small intestinal motility after intracerebroventricular administration to rats.

作者信息

Porreca F, Fulginiti J T, Burks T F

出版信息

Eur J Pharmacol. 1985 Aug 15;114(2):167-73. doi: 10.1016/0014-2999(85)90624-7.

DOI:10.1016/0014-2999(85)90624-7
PMID:4043224
Abstract

The frequency and amplitude of contractions occurring in the duodenum and the jejunum of freely-moving, unanesthetized, female Sprague-Dawley rats were determined by continuously recording intestinal intraluminal pressure. Intracerebroventricular (i.c.v.) administration of saline did not significantly alter the frequency of contractions in either small bowel region when compared with activity observed during a preinjection control period. I.c.v. administration of bombesin (0.1-10 micrograms) produced a dose-related increase in the frequency of duodenal contractions of up to 583% of control. While an increase in jejunal motility was consistently seen with doses of 1 and 10 micrograms, the lowest bombesin dose tested (0.1 microgram) produced a significant decrease in the frequency of contractions in this intestinal area. The intestinal motor effects were seen within the first 30 min after the peptide, and lasted for at least 1 h. Intraperitoneal administration of bombesin, at doses 200 times higher than those given centrally, failed to significantly alter intestinal motility at either recording site. Whether all of the complex intestinal motor effects of bombesin can be directly related to its centrally initiated inhibitory transit effect is unclear; however, the stimulation of contraction frequency in the duodenum at all doses tested suggest that the antitransit effects of bombesin may be, in part, the result of either an increase in the frequency of non-propulsive contractions or a disruption of the normal coordinated propulsive motility pattern of the duodenum.

摘要

通过连续记录肠道腔内压力,测定自由活动、未麻醉的雌性Sprague-Dawley大鼠十二指肠和空肠收缩的频率和幅度。与注射前对照期观察到的活动相比,脑室内(i.c.v.)注射生理盐水对两个小肠区域的收缩频率均无显著影响。脑室内注射蛙皮素(0.1 - 10微克)使十二指肠收缩频率呈剂量依赖性增加,最高可达对照的583%。虽然1微克和10微克剂量的蛙皮素能持续增加空肠运动性,但所测试的最低蛙皮素剂量(0.1微克)却使该肠段的收缩频率显著降低。在注射肽后的最初30分钟内即可观察到肠道运动效应,且至少持续1小时。腹腔注射蛙皮素,剂量比脑室内注射高200倍,在两个记录部位均未显著改变肠道运动性。目前尚不清楚蛙皮素所有复杂的肠道运动效应是否都与其脑内引发的抑制性转运效应直接相关;然而,在所有测试剂量下十二指肠收缩频率的增加表明,蛙皮素的抗转运效应可能部分是由于非推进性收缩频率增加或十二指肠正常协调推进运动模式受到破坏所致。

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Eur J Pharmacol. 1985 Aug 15;114(2):167-73. doi: 10.1016/0014-2999(85)90624-7.
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