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苯丙氨酸-甲硫氨酸-精氨酸-苯丙氨酸-氨基(FMRF酰胺)对小鼠吗啡诱导的结肠推进性运动抑制的影响。

The effect of Phe-Met-Arg-Phe-NH2 (FMRFamide) on morphine-induced inhibition of colonic propulsive motility in mice.

作者信息

Jacoby M B, Jacoby H I, Mathiasen J R, Raffa R B

机构信息

Department of Biological Research, Janssen Research Foundation, Spring House, PA 19477-0776.

出版信息

Neurosci Lett. 1987 Dec 16;83(1-2):128-32. doi: 10.1016/0304-3940(87)90228-x.

Abstract

Morphine and the molluscan neuropeptide Phe-Met-Arg-Phe-NH2 (FMRFamide) were administered to mice alone or in combination intracerebroventricularly (i.c.v.) and the effect on colonic propulsive motility was measured. Both morphine (1.0 microgram, i.c.v.) and FMRFamide (10 and 50 micrograms, i.c.v.) delayed expulsion of a 3 mm glass bead placed in the distal colon of mice compared to vehicle-treated controls. The inhibitory effects of morphine and FMRFamide on expulsion time were additive at the doses used and individually blocked by naloxone. These data suggest that FMRFamide does not antagonize this nonanalgesic effect of morphine, but appears to have opioid agonist properties.

摘要

将吗啡和软体动物神经肽苯丙氨酸-甲硫氨酸-精氨酸-苯丙氨酸-酰胺(FMRF酰胺)单独或联合经脑室注射(i.c.v.)给予小鼠,并测量其对结肠推进性运动的影响。与赋形剂处理的对照组相比,吗啡(1.0微克,经脑室注射)和FMRF酰胺(10微克和50微克,经脑室注射)均延迟了置于小鼠远端结肠的3毫米玻璃珠的排出。在所使用的剂量下,吗啡和FMRF酰胺对排出时间的抑制作用具有相加性,且可被纳洛酮单独阻断。这些数据表明,FMRF酰胺并不拮抗吗啡的这种非镇痛作用,而是似乎具有阿片类激动剂特性。

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