Struthers A D, Millar J A, Beastall G H, McIntosh W B, Reid J L
J Clin Endocrinol Metab. 1983 Feb;56(2):401-4. doi: 10.1210/jcem-56-2-401.
In vitro evidence suggests that calcium is involved in the release of anterior pituitary hormones. Therefore, we studied the effect of the slow calcium channel blocker or calcium antagonist nifedipine on the FSH and LH responses to LRH and the TSH and PRL responses to TRH in vivo. Nine normal male subjects were studied on two occasions, and nifedipine (20 mg, by mouth, or matching placebo) was administered in a randomized single blind manner. Blood pressure and heart rate were measured at 0 and 30 min. The patients then received TRH (200 micrograms) and LRH (100 micrograms) iv. Blood levels of FSH, LH, TSH, and PRL were measured by RIA at 0, 30, 50, 60, and 120 min. Nifedipine lowered diastolic blood pressure significantly (--12 +/- 8 mm Hg; P less than 0.005) and increased heart rate (+ 17 /*- 10 beats/min; P less than 0.005), but had no effect on either baseline hormone levels or the incremental response of any hormone to its secretagogue. In contrast to the results of previous studies with verapamil, nifedipine does not inhibit the release of pituitary hormones. More information is required on the precise intracellular actions of these drugs before they can be used to study the role of calcium in hormone release. Nifedipine, however, may be less likely to influence pituitary function than verapamil.
体外实验证据表明钙参与垂体前叶激素的释放。因此,我们在体内研究了慢钙通道阻滞剂或钙拮抗剂硝苯地平对促卵泡激素(FSH)和促黄体生成素(LH)对促黄体生成素释放激素(LRH)的反应以及促甲状腺激素(TSH)和催乳素(PRL)对促甲状腺激素释放激素(TRH)的反应的影响。对9名正常男性受试者进行了两次研究,以随机单盲方式给予硝苯地平(20毫克,口服,或匹配的安慰剂)。在0和30分钟时测量血压和心率。然后患者静脉注射TRH(200微克)和LRH(100微克)。在0、30、50、60和120分钟时通过放射免疫分析(RIA)测量FSH、LH、TSH和PRL的血药浓度。硝苯地平显著降低舒张压(-12±8毫米汞柱;P<0.005)并增加心率(+17±10次/分钟;P<0.005),但对基线激素水平或任何激素对其促分泌素的增量反应均无影响。与先前使用维拉帕米的研究结果相反,硝苯地平不抑制垂体激素的释放。在这些药物可用于研究钙在激素释放中的作用之前,需要更多关于这些药物精确细胞内作用的信息。然而,硝苯地平可能比维拉帕米更不容易影响垂体功能。