Pazo J H, Levi de Stein M, Jerusalinsky D, Novas M L, Raskovsky S, Tumilasci O R, Medina J H, De Robertis E
Brain Res. 1987 Jun 30;414(2):405-8. doi: 10.1016/0006-8993(87)90025-4.
The effect of chronic administration of haloperidol on alpha 1-, alpha 2-, and beta-adrenoceptors, cholinergic muscarinic, GABAA and benzodiazepine receptors in the cerebral cortex of the rat was investigated. Doses of 0.3 and 2 mg/kg of haloperidol during 7 days increased markedly the density of alpha 1-adrenoceptors without changes in affinity. The alpha 2- and beta-adrenoceptors were not modified after neuroleptic administration. The number of muscarinic receptors were also increased after haloperidol treatment (2 mg/kg/day). However, the GABAA and benzodiazepine binding sites remained unchanged. In the brainstem an increment in the alpha 1-, but not the beta-adrenoceptors was observed. The well known increase in the dopamine receptors in the striatum was confirmed. These observations demonstrate a multireceptor effect of haloperidol in the cerebral cortex.
研究了长期给予氟哌啶醇对大鼠大脑皮质α1、α2和β肾上腺素能受体、胆碱能毒蕈碱受体、GABAA和苯二氮䓬受体的影响。连续7天给予0.3和2mg/kg剂量的氟哌啶醇可显著增加α1肾上腺素能受体的密度,而亲和力不变。给予抗精神病药物后,α2和β肾上腺素能受体未发生改变。氟哌啶醇治疗(2mg/kg/天)后,毒蕈碱受体数量也增加。然而,GABAA和苯二氮䓬结合位点保持不变。在脑干中,观察到α1肾上腺素能受体增加,而β肾上腺素能受体未增加。纹状体中多巴胺受体的众所周知的增加得到了证实。这些观察结果表明氟哌啶醇在大脑皮质具有多受体效应。