Calne D B, Williams A C, Nutt J G, Neophytides A, Eisler T, Teychenne P F
Med J Aust. 1978 Nov 4;2(3 Suppl):25-6. doi: 10.5694/j.1326-5377.1978.tb77384.x.
The response of Parkinsonism to three ergot derivatives which modify dopaminergic transmission was studied. CF 25-397 behaved more as an antagonist than an agonist. Lergotrile was an agonist with therapeutic properties marred by prominent hepatotoxicity. Bromocriptine is an effective anti-Parkinsonian agent, particularly useful in patients with prominent dyskinesia or "on-off" reactions to levodopa; in most patients optimal results have been obtained by combining from 40 to 90 mg of bromocriptine daily with approximately 60% of the previous maximal dose of levodopa. Unfortunately, only some 50% of patients tolerate long-term bromocriptine therapy, but all adverse reactions have been dose dependent and reversible.
研究了帕金森病对三种可改变多巴胺能传递的麦角衍生物的反应。CF 25 - 397表现得更像是拮抗剂而非激动剂。麦角腈是一种激动剂,但其治疗特性因明显的肝毒性而受损。溴隐亭是一种有效的抗帕金森病药物,对左旋多巴有明显运动障碍或“开 - 关”反应的患者尤其有用;在大多数患者中,通过每日联合使用40至90毫克溴隐亭与约60%的先前最大剂量左旋多巴可获得最佳效果。不幸的是,只有约50%的患者能耐受长期溴隐亭治疗,但所有不良反应均与剂量相关且可逆。