Masaoka K, Hosoya N, Mori T, Watanabe H, Ohkura T, Kumasaka T
Nihon Sanka Fujinka Gakkai Zasshi. 1982 Dec;34(12):2155-62.
The present study was designed to examine whether a dopamine agonist, bromocriptine (Brc) exerts similar effects as dopamine (DA) on the pituitary hormones secretion and also to investigate the interaction of these dopaminergic agents and a dopamine receptor antagonist, metoclopramide (MCP) on the DA receptors in the hypothalamic-pituitary axis. Thirty normal cycling women in the midfollicular phase volunteered for this study. Following the administration of Brc (2.5mg, orally) to 13 subjects, a partially significant fall in LH levels, but not in FSH levels, during 4h was observed. DA, infused at a rate of 5 micrograms/kg/min for 4h, induced a significant fall in LH levels between 1 and 4h, but in FSH levels only at 2.5h after the start of infusion in 9 subjects. The amplitude of the spontaneous pulsations of LH secretion which was observed in 8 control subjects, was diminished by DA, while the amplitude seemed to be augmented by Brc. The administration of MCP (10mg, i.v.) to all subjects at 3h during the 4h experimental period caused no observable change in LH and FSH levels. A significant and progressive decline in PRL levels was observed in both Brc-and DA-treated groups of subjects, and this PRL-lowering effect was markedly counteracted by MCP administration in DA-treated group, but not in Brc-treated group. Brc induced a widely varying but significant rise in GH levels, with which MCP did not appear to interfere, whereas DA failed to cause any significant changes in GH levels. These data suggest that Brc, in contrast with DA, seems to be able to increase the pulse amplitude, but not the basal level, of LH and to stimulate GH secretion. Brc is also regarded to be a potent and unique PRL inhibitor, because its PRL-lowering effect cannot be easily antagonized by MCP.
本研究旨在检验多巴胺激动剂溴隐亭(Brc)对垂体激素分泌是否具有与多巴胺(DA)相似的作用,并研究这些多巴胺能药物与多巴胺受体拮抗剂甲氧氯普胺(MCP)在下丘脑 - 垂体轴多巴胺受体上的相互作用。30名处于卵泡中期的正常月经周期女性自愿参与本研究。给13名受试者口服Brc(2.5mg)后,观察到4小时内LH水平有部分显著下降,但FSH水平未下降。以5微克/千克/分钟的速率输注DA 4小时,在9名受试者中,输注开始后1至4小时LH水平显著下降,但FSH水平仅在2.5小时下降。8名对照受试者中观察到的LH分泌自发脉冲幅度被DA降低,而Brc似乎使其增加。在4小时实验期的3小时给所有受试者静脉注射MCP(10mg),LH和FSH水平未观察到明显变化。在接受Brc和DA治疗的两组受试者中均观察到PRL水平显著且逐渐下降,并且在DA治疗组中,MCP给药明显抵消了这种降低PRL的作用,但在Brc治疗组中未出现这种情况。Brc使GH水平有广泛但显著的升高,MCP似乎未对其产生干扰,而DA未能使GH水平发生任何显著变化。这些数据表明,与DA相比,Brc似乎能够增加LH的脉冲幅度而非基础水平,并刺激GH分泌。Brc也被认为是一种强效且独特的PRL抑制剂,因为其降低PRL的作用不易被MCP拮抗。