Murugaiah K, Fleminger S, Theodorou A, Jenner P, Marsden C D
Biochem Pharmacol. 1983 Sep 1;32(17):2495-9. doi: 10.1016/0006-2952(83)90008-4.
Administration of cis-flupenthixol to rats for 18 months enhanced apomorphine-induced stereotyped behaviour, increased the number of specific [3H]spiperone binding sites in striatum and potentiated striatal dopamine stimulated cyclic AMP formation, but did not alter specific [3H]piflutixol binding. Following withdrawal of cis-flupenthixol intake, apomorphine-induced stereotypy returned to control values after 1 month and Bmax for [3H]spiperone binding returned to normal after 3 months. In contrast, the increased dopamine stimulated adenylate cyclase activity remained elevated 6 months after drug removal, but was normal 1 year after drug withdrawal.
给大鼠服用顺式氟哌噻吨18个月,增强了阿扑吗啡诱导的刻板行为,增加了纹状体中特异性[3H]螺哌隆结合位点的数量,并增强了纹状体多巴胺刺激的环磷酸腺苷形成,但未改变特异性[3H]匹莫齐特结合。停止服用顺式氟哌噻吨后,阿扑吗啡诱导的刻板行为在1个月后恢复到对照值,[3H]螺哌隆结合的Bmax在3个月后恢复正常。相比之下,多巴胺刺激的腺苷酸环化酶活性增加在停药后6个月仍保持升高,但在停药1年后恢复正常。