Liao R M, Ko M C
Department of Psychology, National Cheng-Chi University, Taipei, Taiwan.
Chin J Physiol. 1995;38(2):65-73.
Behavioral effects under chronic treatment of haloperidol and SCH23390 were examined for 18 days. Water deprived rats were trained either to perform an operant response on a fixed ratio 20 (FR20) schedule of reinforcement or to lick from a tube in a separate test. Both drugs completely impaired operant responding over all chronic administration days. Whether the lick performance was significantly affected differed depending upon the variable measured in that task. In contrast to the operant results, analysis of the microstructure of licking revealed very distinctive profiles of licking for each drug. Although the lick volume was consistantly reduced by both drugs across days, the decreased numbers of licks first observed were subsequently reversed back to the control level. However, the time courses and the reversal patterns were different for each drug. Haloperidol persistantly reduced the burst size for licking, whereas SCH23390 gradually enlarged it. For interlick interval (ILI) data, haloperidol had more impact on licks with longer ILI without influencing licks of shorter ILI. Contrarily, SCH23390 tended to lengthen the licks with shorter ILI without prolonging them enough to be classified as longer ILI licks. The dissociation of behavioral effects induced by chronic treatment of haloperidol and SCH23390 can be attributed to the drugs' blockade of different DA receptor subtypes. Also, the present study illustrates that using multiple behavioral tasks can be helpful to differentiate the subtle drug actions induced by DA receptor antagonists.
在为期18天的时间里,研究了氟哌啶醇和SCH23390长期治疗下的行为效应。对禁水大鼠进行训练,使其要么按照固定比率20(FR20)强化程序做出操作性反应,要么在单独的测试中从管子中舔舐。在整个长期给药期间,两种药物均完全损害了操作性反应。舔舐表现是否受到显著影响取决于该任务中所测量的变量。与操作性结果相反,对舔舐微观结构的分析显示,每种药物的舔舐情况都非常独特。尽管两种药物在各天中均持续减少了舔舐量,但最初观察到的舔舐次数减少随后又恢复到了对照水平。然而,每种药物的时间进程和恢复模式有所不同。氟哌啶醇持续降低舔舐的爆发大小,而SCH23390则逐渐增大。对于舔舐间隔时间(ILI)数据,氟哌啶醇对ILI较长的舔舐影响更大,而对ILI较短的舔舐没有影响。相反,SCH23390倾向于延长ILI较短的舔舐时间,但延长幅度不足以使其被归类为ILI较长的舔舐。氟哌啶醇和SCH23390长期治疗所诱导的行为效应的分离可归因于药物对不同多巴胺受体亚型的阻断。此外,本研究表明,使用多种行为任务有助于区分多巴胺受体拮抗剂所诱导的细微药物作用。