Lancranjan I
J Neural Transm. 1981;51(1-2):61-82. doi: 10.1007/BF01664005.
Bromocriptine, a potent agonist at Dz receptors, was developed as a therapeutic agent for inhibiting prolactin (PRL) secretion in patients with hyperprolactinemia. Besides, its PRL-suppressive effect and a short-lasting growth hormone (GH)-releasing effect in normal volunteers, bromocriptine has no other endocrine effects in healthy subjects. On the other hand, bromocriptine lowers GH secretion in acromegalic patients and ACTH secretion in some patients with Cushing's disease or Nelson's syndrome. The paper reviews the endocrine actions of bromocriptine in man, in normal and pathological conditions, the bromocriptine's mechanism of action and its clinical applications in endocrinology.
溴隐亭是一种强效的D2受体激动剂,最初被开发用作抑制高泌乳素血症患者泌乳素(PRL)分泌的治疗药物。此外,除了在正常志愿者中具有泌乳素抑制作用和短暂的生长激素(GH)释放作用外,溴隐亭在健康受试者中没有其他内分泌作用。另一方面,溴隐亭可降低肢端肥大症患者的GH分泌以及部分库欣病或尼尔森综合征患者的促肾上腺皮质激素(ACTH)分泌。本文综述了溴隐亭在正常和病理情况下对人体的内分泌作用、作用机制及其在内分泌学中的临床应用。