Kiem D T, Kanyicska B, Stark E, Fekete M I
Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest.
Neuroendocrinology. 1988 Aug;48(2):174-9. doi: 10.1159/000125006.
Cortisol administered at a dose of 25 mg/kg 24 h before measurements decreased the prolactin secretion induced by intraventricularly given opioids (dynorphin, beta-endorphin, Met-enkephalin or D-Met-Pro-enkephalinamide). The effect of cortisol was depressed by actinomycin D pretreatment. The cortisol-induced inhibition of the action of morphine was facilitated in adrenalectomized animals; measuring the effects of increasing doses of cortisol a maximal inhibition was obtained at a dose of 5 mg/kg. The opioid-induced corticosterone secretion was not affected 24 h after a single administration of cortisol. The present results show that the cortisol-induced inhibition of opioid-induced prolactin secretion is dependent on protein synthesis and independent of changes in drug metabolism, and of the type of opiate receptor preferentially affected by the opiate agonists employed.
在测量前24小时以25毫克/千克的剂量给予皮质醇,可减少脑室内注射阿片类物质(强啡肽、β-内啡肽、甲硫氨酸脑啡肽或D-蛋氨酸-脯氨酸-脑啡肽酰胺)所诱导的催乳素分泌。放线菌素D预处理可抑制皮质醇的作用。在肾上腺切除的动物中,皮质醇对吗啡作用的抑制作用增强;测量递增剂量皮质醇的作用时,在5毫克/千克的剂量下可获得最大抑制作用。单次给予皮质醇24小时后,阿片类物质诱导的皮质酮分泌不受影响。目前的结果表明,皮质醇诱导的对阿片类物质诱导的催乳素分泌的抑制作用依赖于蛋白质合成,与药物代谢的变化以及所使用的阿片类激动剂优先作用的阿片受体类型无关。