Yuen B H, Korn G W
Am J Obstet Gynecol. 1980 Dec 1;138(7 Pt 1):738-40. doi: 10.1016/s0002-9378(16)32727-2.
In view of observations suggesting an osmoregulatory role for prolactin (PRL) and the central role of the renin-aldosterone system in the regulation of pressure-volume homeostasis, this study was undertaken to determine whether acute drug-induced alterations in circulating PRL had any effect on mean arterial blood pressure (MAP), serum osmolality, and the renin-aldosterone response during early pregnancy. Bromocriptine suppressed mean baseline PRL by 83% (p > 0.05), whereas chlorpromazine increased it more than twofold (p < 0.05) during a 180-minute study period. MAP, mean serum osmolality, plasma renin activity, and aldosterone concentrations were not significantly different from mean baseline values after the administration of either drug. These data suggest that, during early pregnancy, the renin-aldosterone axis is independent of PRL and resistant to the beta-adrenergic agonist effect of chlorpromazine.
鉴于有观察结果表明催乳素(PRL)具有渗透调节作用,且肾素 - 醛固酮系统在压力 - 容量稳态调节中起核心作用,本研究旨在确定妊娠早期循环中PRL的急性药物诱导变化是否对平均动脉血压(MAP)、血清渗透压以及肾素 - 醛固酮反应有任何影响。在一项180分钟的研究期间,溴隐亭使平均基础PRL降低了83%(p>0.05),而氯丙嗪使其增加了两倍多(p<0.05)。给予任何一种药物后,MAP、平均血清渗透压、血浆肾素活性和醛固酮浓度与平均基础值均无显著差异。这些数据表明,在妊娠早期,肾素 - 醛固酮轴独立于PRL,且对氯丙嗪的β - 肾上腺素能激动剂作用具有抗性。