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一种药物-药物条件反射范式揭示了多种抗精神病药物与尼古丁的相互作用。

A drug-drug conditioning paradigm reveals multiple antipsychotic-nicotine interactions.

作者信息

Feng Min, Sparkman Nathan L, Sui Nan, Li Ming

机构信息

1 Department of Viral Immunology, Institute of Medical Biology, Chinese Academy of Medical Sciences, Peking Union Medical College, Kunming, China.

2 Key Laboratory of Mental Health, Institute of Psychology, Chinese Academy of Sciences, Beijing, China.

出版信息

J Psychopharmacol. 2017 Apr;31(4):474-486. doi: 10.1177/0269881116681471. Epub 2016 Dec 14.

Abstract

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.

摘要

临床研究表明,精神分裂症患者使用尼古丁与抗精神病药物之间存在相互影响。本研究采用条件性回避反应(CAR)试验(一种抗精神病作用的行为试验),研究了尼古丁与氟哌啶醇或氯氮平之间的具体药物相互作用。在获得回避反应后,大鼠首先在溶剂、尼古丁(0.2、0.4毫克/千克,皮下注射)、氟哌啶醇(0.025、0.05毫克/千克,皮下注射)、氯氮平(5.0、10.0毫克/千克,皮下注射)或尼古丁与氟哌啶醇或尼古丁与氯氮平的组合下连续测试7天。之后,在CAR试验中用尼古丁(0.2毫克/千克)、氟哌啶醇(0.025毫克/千克)或氯氮平(5.0毫克/千克)对它们进行激发试验,以评估氟哌啶醇或氯氮平是否影响尼古丁对回避反应的行为效应,以及尼古丁是否改变氟哌啶醇和氯氮平的回避抑制效应。在七天的回避药物测试期间,尼古丁没有改变氟哌啶醇或氯氮平的回避抑制效应。然而,在激发试验中,预先给予尼古丁治疗(0.2毫克/千克)减弱了氟哌啶醇(0.05毫克/千克)对回避反应的致敏作用。另一方面,预先给予氟哌啶醇治疗增加了尼古丁(0.2毫克/千克)的回避干扰作用,甚至使0.4毫克/千克的尼古丁表现出“获得性”回避抑制效应。尼古丁与氯氮平联合治疗对回避反应和运动活动未产生任何可检测到的相互作用效应。这些发现表明,尼古丁能够改变氟哌啶醇的长期抗精神病疗效,而氟哌啶醇可以改变尼古丁的行为效应。氯氮平和尼古丁相互影响的可能性较小。

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