Ferrari C, Rampini P, Paracchi A, Boghen M, Mailland F
Eur J Clin Pharmacol. 1985;27(6):707-11. doi: 10.1007/BF00547054.
The endocrine effects of a relatively potent dopaminergic agent, dihydroergokryptine, have been studied in normal subjects, and in hyperprolactinaemic and acromegalic patients. A single 6 mg oral dose of the drug caused a marked, long lasting fall in prolactin (PRL) plasma levels in healthy subjects, in hyperprolactinaemic patients and in normoprolactinaemic acromegalics. Growth hormone (GH) levels decreased in 1-DOPA - responder, acromegalic patients, but dihydroergokryptine did not affect GH levels in normal volunteers or in 1-DOPA non-responder, acromegalic patients. The PRL- and GH- lowering activity of 6 mg dihydroergokryptine was significantly greater than that of 6 mg dihydroergocristine, and was similar to that of an oral dose of 500 mg 1-DOPA.
一种相对强效的多巴胺能药物——二氢麦角隐亭的内分泌效应,已在正常受试者、高泌乳素血症患者和肢端肥大症患者中进行了研究。单次口服6毫克该药物可使健康受试者、高泌乳素血症患者和泌乳素水平正常的肢端肥大症患者的血浆泌乳素(PRL)水平显著且持久下降。在对左旋多巴有反应的肢端肥大症患者中,生长激素(GH)水平降低,但二氢麦角隐亭对正常志愿者或对左旋多巴无反应的肢端肥大症患者的GH水平没有影响。6毫克二氢麦角隐亭降低PRL和GH的活性明显大于6毫克二氢麦角克碱,且与口服500毫克左旋多巴的效果相似。