Brambilla F, Scarone S, Pugnetti L, Massironi R, Penati G, Nobile P
Psychiatry Res. 1983 Mar;8(3):159-69. doi: 10.1016/0165-1781(83)90059-8.
Ten chronic schizophrenic patients were given bromocriptine in doses increasing from 1.25 to 5 mg over 6 days (the low-dose therapy) and then up to 40 mg over 15 days (the high-dose therapy). Psychopathological status was assessed using the Brief Psychiatric Rating Scale, twice daily the first 6 days, and every 2 days thereafter. The prolactin (PRL) response to haloperidol stimulation (1 mg i.v.) was measured in five cases before and 3 days after the end of high-dose therapy, and in one patient before and 3 days after the end of low-dose therapy. Electroencephalographic sleep studies were carried out before therapy and every 2 nights during low-dose therapy in five patients, and in two cases during high-dose therapy. Bromocriptine therapy modified neither clinical symptomatology nor sleep patterns. The PRL response to haloperidol after therapy was markedly lower than that before therapy in the five patients treated with high doses, and markedly higher in the single patient tested who was treated only with low-dose therapy.
10名慢性精神分裂症患者接受了溴隐亭治疗,剂量在6天内从1.25毫克增加至5毫克(低剂量治疗),然后在15天内增加至40毫克(高剂量治疗)。使用简明精神病评定量表评估精神病理状态,最初6天每天评估两次,此后每2天评估一次。在高剂量治疗结束前及结束后3天,对5例患者测量了催乳素(PRL)对氟哌啶醇刺激(静脉注射1毫克)的反应;在低剂量治疗结束前及结束后3天,对1例患者进行了测量。在5例患者治疗前及低剂量治疗期间每2晚进行一次脑电图睡眠研究,在2例患者高剂量治疗期间进行了研究。溴隐亭治疗既未改变临床症状,也未改变睡眠模式。在接受高剂量治疗的5例患者中,治疗后PRL对氟哌啶醇的反应明显低于治疗前;在仅接受低剂量治疗的1例受试患者中,PRL反应明显高于治疗前。