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氯氮平的行为效应:与硫利达嗪、氯丙嗪、氟哌啶醇及氯氮䓬在松鼠猴中的比较

Behavioral effects of clozapine: comparison with thioridazine, chlorpromazine, haloperidol and chlordiazepoxide in squirrel monkeys.

作者信息

Spealman R D, Kelleher R T, Goldberg S R, DeWeese J, Goldberg D M

出版信息

J Pharmacol Exp Ther. 1983 Jan;224(1):127-34.

PMID:6848739
Abstract

The behavioral effects of the antipsychotic drug, clozapine, were compared with those of thioridazine, chlorpromazine, haloperidol and chlordiazepoxide. Behavior of squirrel monkeys was controlled by different consequences of a lever-pressing response (presentation of food, presentation of electric shock or termination of a stimulus associated with electric shock) under different schedules of reinforcement (a fixed-interval schedule or a multiple schedule with alternating fixed-ratio and fixed-interval components). The effects of thioridazine (0.2-24.6 mumol/kg), chlorpromazine (0.03-2.8 mumol/kg) and haloperidol (0.001-0.08 mumol/kg) were largely independent of the type of schedule or the type of consequent event that maintained responding: each drug produced dose-related decreases in responding under all conditions in which they were studied. Clozapine (0.1-9.2 mumol/kg) and chlordiazepoxide (0.9-167.4 mumol/kg) also only decreased responding under most schedule conditions; however, intermediate doses of either drug markedly increased responding maintained by presentation of food under the fixed-interval schedule (whether programmed singly or as a component of the multiple schedule). Only clozapine increased responding maintained by presentation of electric shock under the fixed-interval schedule. Thus, the behavioral effects of clozapine differed qualitatively from those of representative antipsychotic and antianxiety drugs.

摘要

将抗精神病药物氯氮平的行为效应与硫利达嗪、氯丙嗪、氟哌啶醇和氯氮卓的行为效应进行了比较。松鼠猴的行为通过不同强化程序(固定间隔程序或具有交替固定比率和固定间隔成分的多重程序)下杠杆按压反应的不同后果(给予食物、给予电击或终止与电击相关的刺激)来控制。硫利达嗪(0.2 - 24.6 μmol/kg)、氯丙嗪(0.03 - 2.8 μmol/kg)和氟哌啶醇(0.001 - 0.08 μmol/kg)的效应在很大程度上与维持反应的程序类型或后续事件类型无关:在研究它们的所有条件下,每种药物都产生与剂量相关的反应减少。氯氮平(0.1 - 9.2 μmol/kg)和氯氮卓(0.9 - 167.4 μmol/kg)在大多数程序条件下也仅减少反应;然而,这两种药物的中等剂量在固定间隔程序(无论是单独编程还是作为多重程序的一个成分)下由给予食物维持的反应中显著增加。只有氯氮平在固定间隔程序下由给予电击维持的反应中增加反应。因此,氯氮平的行为效应在质量上与代表性的抗精神病药物和抗焦虑药物不同。

相似文献

1
Behavioral effects of clozapine: comparison with thioridazine, chlorpromazine, haloperidol and chlordiazepoxide in squirrel monkeys.氯氮平的行为效应:与硫利达嗪、氯丙嗪、氟哌啶醇及氯氮䓬在松鼠猴中的比较
J Pharmacol Exp Ther. 1983 Jan;224(1):127-34.
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引用本文的文献

1
Avoidance disruptive effect of clozapine and olanzapine is potentiated by increasing the test trials: further test of the motivational salience hypothesis.避免氯氮平和奥氮平的破坏效应可以通过增加测试试验来增强:动机显著性假设的进一步检验。
Pharmacol Biochem Behav. 2013 Jan;103(3):467-73. doi: 10.1016/j.pbb.2012.09.013. Epub 2012 Sep 28.
2
Clozapine, but not olanzapine, disrupts conditioned avoidance response in rats by antagonizing 5-HT2A/2C receptors.氯氮平而非奥氮平通过拮抗 5-HT2A/2C 受体破坏大鼠的条件性回避反应。
J Neural Transm (Vienna). 2012 Apr;119(4):497-505. doi: 10.1007/s00702-011-0722-6. Epub 2011 Oct 11.
3
Olanzapine and risperidone disrupt conditioned avoidance responding by selectively weakening motivational salience of conditioned stimulus: further evidence.
奥氮平与利培酮通过选择性削弱条件刺激的动机显著性而破坏条件回避反应:进一步的证据。
Pharmacol Biochem Behav. 2011 Mar;98(1):155-60. doi: 10.1016/j.pbb.2010.12.018. Epub 2010 Dec 29.
4
Olanzapine and risperidone disrupt conditioned avoidance responding in phencyclidine-pretreated or amphetamine-pretreated rats by selectively weakening motivational salience of conditioned stimulus.奥氮平和利培酮通过选择性削弱条件刺激的动机显著性,破坏苯环利定预处理或苯丙胺预处理大鼠的条件性回避反应。
Behav Pharmacol. 2009 Feb;20(1):84-98. doi: 10.1097/FBP.0b013e3283243008.
5
Response decrement patterns after neuroleptic and non-neuroleptic drugs.
Psychopharmacology (Berl). 1986;89(1):98-104. doi: 10.1007/BF00175198.
6
Effects of some dibenzo-azepines on suppressed and nonsuppressed behavior of squirrel monkeys.某些二苯并氮杂䓬对松鼠猴抑制和非抑制行为的影响。
Psychopharmacology (Berl). 1985;85(2):129-32. doi: 10.1007/BF00428400.
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Clozapine. A review of its pharmacological properties, and therapeutic use in schizophrenia.氯氮平:其药理特性及在精神分裂症治疗中的应用综述
Drugs. 1990 Nov;40(5):722-47. doi: 10.2165/00003495-199040050-00007.