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首页> 外文期刊>Journal of psychopharmacology >A drug-drug conditioning paradigm reveals multiple antipsychotic-nicotine interactions
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A drug-drug conditioning paradigm reveals multiple antipsychotic-nicotine interactions

机译:药物调理范式揭示了多种抗精神病尼古丁相互作用

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Clinical studies indicate a reciprocal impact between nicotine use and antipsychotic medications in patients with schizophrenia. The present study used a conditioned avoidance response (CAR) test (a behavioral test of antipsychotic effect) and examined the specific drug-drug interactions between nicotine and haloperidol or clozapine. Following acquisition of the avoidance response, rats were first tested under either vehicle, nicotine (0.2, 0.4 mg/kg, sc), haloperidol (0.025, 0.05 mg/kg, sc), clozapine (5.0, 10.0 mg/kg, sc), or a combination of nicotine and haloperidol or nicotine and clozapine for seven consecutive days. Afterward, they were challenged with nicotine (0.2 mg/kg), haloperidol (0.025 mg/kg), or clozapine (5.0 mg/kg) in the CAR to assess if haloperidol or clozapine affected the behavioral effect of nicotine on avoidance response and if nicotine altered the avoidance suppressive effect of haloperidol and clozapine. During the seven avoidance drug test days, nicotine did not alter the avoidance suppressive effect of haloperidol or clozapine. However, in the challenge test, prior nicotine treatment (0.2 mg/kg) attenuated haloperidol's (0.05 mg/kg) sensitized effect on avoidance response. On the other hand, prior haloperidol treatment increased nicotine's (0.2 mg/kg) avoidance disruptive effect, and even engendered nicotine 0.4 mg/kg to exhibit an acquired avoidance suppressive effect. The combined nicotine and clozapine treatment did not produce any detectable interactive effects on avoidance response and motor activity. These findings suggest that nicotine is capable of altering the long-term antipsychotic efficacy of haloperidol, while haloperidol can alter the behavioral effects of nicotine. Clozapine and nicotine are less likely to influence each other.
机译:临床研究表明尼古丁使用与精神分裂症患者抗精神病药物之间的互殖影响。本研究使用了条件避免响应(轿车)试验(抗精神病效应的行为试验),并检查了尼古丁和氟哌啶醇或氯氮平之间的特定药物 - 药物相互作用。在获取避免响应之后,首先在任一载体,尼古丁(0.2,0.4mg / kg,sc),氟哌啶醇(0.025,0.05mg / kg,sc),氯氮平(5.0,10.0mg / kg,sc)下测试大鼠或连续七天的尼古丁和氟哌啶醇或尼古丁和氯氮平的组合。之后,它们在汽车中挑战尼古丁(0.2mg / kg),氟哌啶醇(0.025mg / kg)或氯氮平(5.0mg / kg),以评估氟哌啶醇或氯氮平是否影响尼古丁对避免响应的行为效应,如果尼古丁改变了氟哌啶醇和氯氮平的避免抑制作用。在七次避免药物测试日内,尼古丁没有改变氟哌啶醇或氯氮平的避免抑制作用。然而,在挑战试验中,先前的尼古丁治疗(0.2mg / kg)减毒的氟哌啶醇(0.05mg / kg)对避免反应的敏化作用。另一方面,先前的氟哌啶醇治疗增加了尼古丁(0.2mg / kg)避免破坏性效果,甚至有发芽的尼古丁0.4mg / kg表现出获得的避税抑制效果。合并的尼古丁和氯氮平治疗没有对避免响应和运动活动产生任何可检测的互动效果。这些发现表明,尼古丁能够改变氟哌啶醇的长期抗精神病药物,而氟哌啶醇可以改变尼古丁的行为作用。氯氮平和尼古丁不太可能互相影响。

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