George S R, Kertesz M
Peptides. 1986 Mar-Apr;7(2):277-81. doi: 10.1016/0196-9781(86)90225-1.
The effect of dopamine receptor stimulation by administration of the dopamine analogue bromocriptine on Met-enkephalin-LI was examined in rat hypothalamus, and neurointermediate and anterior lobes of pituitary. Bromocriptine treatment resulted in a dramatic decline of Met-enkephalin-LI in neurointermediate pituitary which was significant by 3 days of treatment. Maximal reduction of Met-enkephalin-LI ranged between 60-70% of pretreatment values and was maintained as long as bromocriptine was administered (4 weeks), with no evidence of desensitization or "escape." The effects of bromocriptine on neurointermediate lobe were of long duration and persisted for at least 4 days after discontinuation of treatment. No significant effects of bromocriptine were detected on Met-enkephalin-LI in hypothalamus or anterior pituitary. Whether these differences represent truly different regional regulation of Met-enkephalin-LI or whether the changes are more sensitively reflected in an area such as neurointermediate lobe that largely consists of nerve terminals, remains to be shown.
通过给予多巴胺类似物溴隐亭刺激多巴胺受体,研究其对大鼠下丘脑、垂体神经中间叶和垂体前叶中甲硫氨酸脑啡肽免疫反应性(Met-enkephalin-LI)的影响。溴隐亭治疗导致垂体神经中间叶中甲硫氨酸脑啡肽免疫反应性显著下降,治疗3天时下降明显。甲硫氨酸脑啡肽免疫反应性的最大降幅为治疗前值的60%-70%,且只要给予溴隐亭(4周),这种下降就会持续,没有脱敏或“逃逸”的迹象。溴隐亭对神经中间叶的作用持续时间长,停药后至少持续4天。未检测到溴隐亭对下丘脑或垂体前叶中甲硫氨酸脑啡肽免疫反应性有显著影响。这些差异是代表甲硫氨酸脑啡肽免疫反应性真正不同的区域调节,还是这些变化在主要由神经末梢组成的神经中间叶等区域更敏感地反映出来,仍有待证明。