Kubota T
Nihon Sanka Fujinka Gakkai Zasshi. 1984 Jul;36(7):1017-26.
The purpose of this study was to investigate hypothalamic dopaminergic activity in pregnant women after the administration of metoclopramide (MCP), a dopamine receptor blocker, and to investigate the effects of MCP on the placental steroid and peptide hormones, and to clarify the prolactin (PRL) releasing mechanism in the hypothalamo-pituitary axis during pregnancy using dopaminergic agents and TRH. The following results were obtained. The plasma PRL levels following intravenous MCP remained significantly elevated for 180 minutes (p less than 0.001-0.05) in all groups as compared to the control group, but there were no significant differences between early and late pregnant groups, and between pregnant and nonpregnant groups. Therefore, the dopaminergic activity of the hypothalamus remained unchanged during pregnancy as well as in the nonpregnant state. The administration of MCP or a sudden increase in plasma PRL had no effect on the maternal plasma estradiol-17 beta, progesterone, HCG or HPL during pregnancy. PRL release from the pituitary by MCP was suppressed significantly (p less than 0.01) by pretreatment with bromocriptine. PRL releasing activity of MCP 10mg was significantly higher (p less than 0.01-0.05) than that of TRH 500 micrograms in the pregnant women.
本研究的目的是调查给予多巴胺受体阻滞剂甲氧氯普胺(MCP)后孕妇下丘脑多巴胺能活性,研究MCP对胎盘甾体和肽类激素的影响,并使用多巴胺能药物和促甲状腺激素释放激素(TRH)阐明孕期下丘脑 - 垂体轴中催乳素(PRL)的释放机制。获得了以下结果。与对照组相比,所有组静脉注射MCP后血浆PRL水平在180分钟内仍显著升高(p小于0.001 - 0.05),但孕早期和孕晚期组之间以及孕妇和非孕妇组之间无显著差异。因此,孕期下丘脑的多巴胺能活性与非孕期一样保持不变。孕期给予MCP或血浆PRL突然升高对母体血浆雌二醇 - 17β、孕酮、人绒毛膜促性腺激素(HCG)或人胎盘催乳素(HPL)无影响。用溴隐亭预处理可显著抑制MCP诱导的垂体PRL释放(p小于0.01)。在孕妇中,10mg MCP的PRL释放活性显著高于500μg TRH(p小于0.01 - 0.05)。