Clemens J A, Sawyer B D, Cerimele B
Department of Physiological Research, Lilly Research Laboratories, Indianapolis, Indiana 46206.
Endocrinology. 1977 Mar;100(3):692-8. doi: 10.1210/endo-100-3-692.
Administration of a new specific serotonin uptake inhibitor, fluoxetine, depressed the firing rate of raphe neurons. A highly significant increase in serum prolactin levels was observed after ip injection of 30 mg/kg of 5-hydroxytryptophan (5-HTP) in male or female rats pretreated with 10 mg/kg (ip) of fluoxetine. Neither 5-HTP nor fluoxetine given separately had any effect on serum prolactin levels. In animals pretreated with methysergide the combination of fluoxetine and 5-HTP did not increase significantly serum levels of prolactin. In addition, the serotonin agonist quipazine elevated significantly serum prolactin levels in male and female rats. The results of this study strengthen the idea that 5-HTP is acting via serotonin-containing neurons that influence anterior pituitary prolactin release, and that serotonin receptor activation leads to prolactin release.
给予一种新的特异性5-羟色胺摄取抑制剂氟西汀后,中缝核神经元的放电频率降低。在经腹腔注射10mg/kg(腹腔注射)氟西汀预处理的雄性或雌性大鼠中,腹腔注射30mg/kg的5-羟色氨酸(5-HTP)后,血清催乳素水平显著升高。单独给予5-HTP或氟西汀对血清催乳素水平均无任何影响。在用麦角酰二乙胺预处理的动物中,氟西汀和5-HTP的组合并未显著提高血清催乳素水平。此外,5-羟色胺激动剂喹哌嗪可显著提高雄性和雌性大鼠的血清催乳素水平。本研究结果强化了以下观点:5-HTP通过影响垂体前叶催乳素释放的含5-羟色胺神经元起作用,且5-羟色胺受体激活导致催乳素释放。