Bluet-Pajot M T, Mounier F, Durand D, Kordon C
U. 159 INSERM, Centre Paul Broca, Paris, France.
J Endocrinol. 1990 Nov;127(2):191-6. doi: 10.1677/joe.0.1270191.
The effects of dopamine on GH release were investigated both in vivo in freely moving intact rats and in rats with a mediobasal hypothalamic lesion, and in vitro in a perifusion system using dispersed male rat pituitary cells kept in primary culture. In vivo, dopamine (5 mg/kg body weight) induced a rapid and very transient increase in plasma GH levels in lesioned but not in intact rats. This increase was markedly inhibited by a prior injection of the D1 antagonist SCH 23390 (0.5 mg/kg) but not of the D2 antagonist domperidone (0.5 mg/kg). The D1 agonist SKF 38393 induced a dose-dependent stimulation of GH release in lesioned rats, and the effect obtained with a dose of 5 mg/kg was abolished by pretreatment with SCH 23390 (0.5 mg/kg). In vitro, dopamine (0.1 mumol/l) and SKF 38393 (0.1 mumol/l) provoked a rapid and reversible release of GH from superfused rat pituitary cells; this effect was markedly inhibited by simultaneous superfusion of SCH 23390 (1 mumol/l). These findings indicate that dopamine can stimulate basal GH release at the pituitary level and that this stimulation is mediated by D1 but not by D2 receptors. They also support the hypothesis that unidentified hypothalamic neurohormones may modulate this effect.
在自由活动的完整大鼠和患有下丘脑中间基底部损伤的大鼠体内,以及在使用原代培养的分散雄性大鼠垂体细胞的灌流系统中,研究了多巴胺对生长激素(GH)释放的影响。在体内,多巴胺(5毫克/千克体重)可使损伤大鼠而非完整大鼠的血浆GH水平迅速且非常短暂地升高。预先注射D1拮抗剂SCH 23390(0.5毫克/千克)可显著抑制这种升高,但注射D2拮抗剂多潘立酮(0.5毫克/千克)则无此作用。D1激动剂SKF 38393可诱导损伤大鼠的GH释放呈剂量依赖性刺激,用5毫克/千克剂量获得的效应可被预先用SCH 23390(0.5毫克/千克)处理所消除。在体外,多巴胺(0.1微摩尔/升)和SKF 38393(0.1微摩尔/升)可促使灌流的大鼠垂体细胞快速且可逆地释放GH;同时灌流SCH 23390(1微摩尔/升)可显著抑制这种效应。这些发现表明,多巴胺可在垂体水平刺激基础GH释放,且这种刺激是由D1受体而非D2受体介导的。它们还支持这样一种假说,即未确定的下丘脑神经激素可能调节这种效应。