Peillon F, Cesselin F, Bression D, Zygelman N, Brandi A M, Nousbaum A, Mauborgne A
J Clin Endocrinol Metab. 1979 Nov;49(5):737-41. doi: 10.1210/jcem-49-5-737.
To determine the site of action of dopaminergic drugs on human PRL and GH release from pituitary adenomas, five PRL-and five GH-secreting adenomas were incubated with and without dopamine and L-dopa. Bromocriptine was also tested in order to compare its effect to that of the other drugs. In all of the experiments except one, a decrease of PRL, which was often statistically significant, was observed. When pooling the results of the PRL-secreting adenomas, the mean levels of PRL with dopamine, L-dopa, and bromocriptine were, respectively, 49%, 55%, and 60% of the control levels. In the GH-secreting adenomas, they were 60%, 67%, and 55% of that of the control. For GH, a decrease of the release was observed in four out of five GH-secreting adenomas. When pooling the results from these tumors, the mean levels of GH with dopamine, L-dopa, and bromocriptine were, respectively, 63%, 76%, and 64% of the control levels. In one case, a significant increase of GH was observed with the three dopaminergic drugs. This study produced the following conclusions. 1) Dopamine acts directly on PRL and GH release from human pituitary adenomas; in vitro, L-dopa effects are similar (its action probably occurs after conversion to catecholamines). These observations strongly suggest the presence of dopaminergic membrane receptors on human lactotroph and somatotroph adenomatous pituitary cells. 2) In vitro hormonal results are in good agreement with in vivo dynamic tests using L-dopa and bromocriptine. 3) The paradoxical effect of dopaminergic drugs on GH secretion in acromegalic patients may be attributed to modified dopamine membrane receptors. However, the paradoxical response is not a constant feature in acromegaly, and its mechanism needs further investigations.
为确定多巴胺能药物对人垂体腺瘤分泌催乳素(PRL)和生长激素(GH)的作用位点,将5例分泌PRL的腺瘤和5例分泌GH的腺瘤分别在有或无多巴胺及左旋多巴(L -多巴)的情况下进行孵育。还对溴隐亭进行了测试,以便将其效果与其他药物的效果进行比较。在除一项实验外的所有实验中,均观察到PRL下降,且这种下降通常具有统计学意义。汇总分泌PRL腺瘤的实验结果时,使用多巴胺、L -多巴和溴隐亭时PRL的平均水平分别为对照水平的49%、55%和60%。在分泌GH的腺瘤中,这些水平分别为对照水平的60%、67%和55%。对于GH,在5例分泌GH的腺瘤中有4例观察到释放减少。汇总这些肿瘤的实验结果时,使用多巴胺、L -多巴和溴隐亭时GH的平均水平分别为对照水平的63%、76%和64%。在1例中,使用这三种多巴胺能药物时观察到GH显著增加。本研究得出以下结论。1)多巴胺直接作用于人垂体腺瘤分泌PRL和GH;在体外,L -多巴的作用相似(其作用可能在转化为儿茶酚胺后发生)。这些观察结果强烈提示人催乳素细胞和生长激素细胞垂体腺瘤细胞膜上存在多巴胺能受体。2)体外激素实验结果与使用L -多巴和溴隐亭的体内动态试验结果高度一致。3)多巴胺能药物对肢端肥大症患者GH分泌的矛盾作用可能归因于多巴胺膜受体的改变。然而,这种矛盾反应在肢端肥大症中并非恒定特征,其机制需要进一步研究。