Silvestrini F, Liuzzi A, Chiodini P G
Pharmacology. 1978;16 Suppl 1:78-87. doi: 10.1159/000136810.
The effects of ergot alkaloids (mainly bromocriptine) on the secretion of GH and PRL in normal subjects and in pathological conditions (i.e. acromegaly and hyperprolactinemic states) are discussed. In the normal subjects, bromocriptine releases GH whereas in about 50% of acromegalics it causes a marked and long-lasting inhibition of the hormone secretion. PRL release is reduced by the drug both in normal subjects and in hyperprolactinemic states. Physiopathological studies in the humans indicate that, according to the experimental data, bromocriptine inhibits GH release in acromegaly and PRL secretion through a dopaminergic mechanism of action playing at the pituitary level. Data are reported on the effectiveness of bromocriptine in the medical treatment of acromegaly and of hyperprolactinemic states.
本文讨论了麦角生物碱(主要是溴隐亭)对正常受试者以及病理状态(如肢端肥大症和高泌乳素血症)下生长激素(GH)和泌乳素(PRL)分泌的影响。在正常受试者中,溴隐亭可释放GH,而在约50%的肢端肥大症患者中,它会引起该激素分泌的显著且持久抑制。在正常受试者和高泌乳素血症状态下,该药物均可降低PRL释放。人体生理病理学研究表明,根据实验数据,溴隐亭通过作用于垂体水平的多巴胺能机制抑制肢端肥大症患者的GH释放和PRL分泌。文中报告了溴隐亭在肢端肥大症和高泌乳素血症药物治疗中的有效性数据。