Müller E E, Genazzani A R, Murru S, Fioretti P
Acta Endocrinol (Copenh). 1977 Sep;86(1):33-41. doi: 10.1530/acta.0.0860033.
In women with physiological puerperal hyperprolactinaemia, acute administration of Piribedil (100 mg po), a drug which stimulates dopamine receptor sites, was as effective as that of 2-Br-alpha-ergocryptine (CB 154, 5 mg po) in suppressing the elevated baseline plasma prolactin (PRL) levels. In two hyperprolactinaemic women with radiological evidence of an intrasellar pituitary tumour, Piribedil (100 mg po), in contrast to CB 154 (5 mg po), failed to modify plasma PRL levels, whereas in 3 other hyperprolactinaemic women with no radiological evidence of pituitary tumour, its effect was not clear-cut, even though it could not be differentiated from that of CB 154. These results indicate that Piribedil is an effective suppressor of plasma PRL levels in the human and suggest that its action is more evident in puerperal than in pathological hyperprolactinaemia.
在患有生理性产后高催乳素血症的女性中,急性给予刺激多巴胺受体位点的药物吡贝地尔(口服100毫克),在抑制升高的基础血浆催乳素(PRL)水平方面与2-溴-α-麦角隐亭(CB 154,口服5毫克)效果相同。在两名有蝶鞍内垂体瘤放射学证据的高催乳素血症女性中,与CB 154(口服5毫克)相比,吡贝地尔(口服100毫克)未能改变血浆PRL水平,而在另外三名无垂体瘤放射学证据的高催乳素血症女性中,其效果并不明确,尽管无法与CB 154的效果区分开来。这些结果表明吡贝地尔是人体血浆PRL水平的有效抑制剂,并表明其作用在产后比在病理性高催乳素血症中更明显。