Raffa R B
Department of Biological Research, Janssen Research Foundation, Spring House, PA 19477-0776.
Peptides. 1989 Mar-Apr;10(2):403-6. doi: 10.1016/0196-9781(89)90050-8.
Morphine and the molluscan neuropeptide Phe-Met-Arg-Phe-NH2 (FMRFamide) were administered to mice alone or in combination intracerebroventricularly (ICV) and the effect on locomotor activity was measured. Morphine given alone (0.5 micrograms) significantly increased horizontal locomotor activity compared to vehicle-treated controls. FMRFamide at low doses (0.01-10 micrograms) had no effect of its own, but blocked the morphine-induced increase in horizontal locomotor activity. Unlike the opiate antagonist naloxone (1.0 micrograms), FMRFamide (up to 10 micrograms) had no effect on morphine-induced decrease in vertical activity. These data further support a role for FMRFamide as a modulator of opiate action, but comparison to naloxone suggests that FMRFamide might not act as a pure competitive antagonist of this opiate effect.
将吗啡和软体动物神经肽苯丙氨酸 - 蛋氨酸 - 精氨酸 - 苯丙氨酸 - 酰胺(FMRF酰胺)单独或联合经脑室注射(ICV)给小鼠,并测量其对运动活性的影响。与溶剂处理的对照组相比,单独给予吗啡(0.5微克)可显著增加水平运动活性。低剂量(0.01 - 10微克)的FMRF酰胺自身无作用,但可阻断吗啡诱导的水平运动活性增加。与阿片拮抗剂纳洛酮(1.0微克)不同,FMRF酰胺(高达10微克)对吗啡诱导的垂直活性降低无作用。这些数据进一步支持FMRF酰胺作为阿片作用调节剂的作用,但与纳洛酮的比较表明,FMRF酰胺可能并非该阿片效应的纯粹竞争性拮抗剂。