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氟哌啶醇可减弱哌醋甲酯和莫达非尼引起的行为敏化和认知增强。

Haloperidol attenuates Methylphenidate and Modafinil induced behavioural sensitization and cognitive enhancement.

机构信息

Department of Pharmacology, Faculty of Pharmacy, Federal Urdu University of Arts, Science and Technology , Karachi-75400, Karachi, Pakistan.

出版信息

Metab Brain Dis. 2018 Jun;33(3):893-906. doi: 10.1007/s11011-018-0190-x. Epub 2018 Feb 22.

Abstract

Previous studies have demonstrated that repeated psychostimulant administration produces behavioural sensitization and cognitive tolerance. Brain dopaminergic system and the involvement of dopamine D-receptors are considered to be important in psychostimulant-induced sensitization. Study designed to compared the motor activity by using familiar and novel enviroments and cognitive effects by water maze and passive avoidance test after long term administration of methylphenidate(at the dose 0.6 mg/kg/day, 2.5 mg/kg/day and 10 mg/kg/day) and modafinil (50 mg/kg/day, 64 mg/kg/day and 75 mg/kg/day) in rats. The effects of challenge dose of haloperidol (at the dose of 1 mg/kg i.p.) has monitored to visualize any subsensitization or supersensitization of D receptors. We found that motor activity and cognitive performance was increased in all doses and sensitization effect was more pronounced after 13 days of drug administration were greater at high than low and medium doses.Challenge dose of haloperidol attenuate motor activity in familiar and novel environment and impaired cognition in water maze and passive avoidance test in all treated rats. The effect of Haloperidol in high dose treated rats were however somewhat greater than low and medium dose treated rats following methylphenidate and modafinil administration. Increased response of haloperidol in methylphenidate treated rats can be explained in term of supersensitization of D receptors which is greater in high dose treated rats. The results show that the role of D receptors to develop side effects such as behavioural sensitization and cognitive tolerance by the long term administration of psychostimulants is of sufficient importance and helpful in understanding the mechanisms underlying the undesirable effects of psychostimulants.

摘要

先前的研究表明,重复给予精神兴奋剂会产生行为敏化和认知耐受。脑多巴胺能系统和多巴胺 D 受体的参与被认为在精神兴奋剂引起的敏化中很重要。本研究旨在比较长期给予哌甲酯(0.6mg/kg/天、2.5mg/kg/天和 10mg/kg/天)和莫达非尼(50mg/kg/天、64mg/kg/天和 75mg/kg/天)后,使用熟悉和新颖环境进行的运动活动以及水迷宫和被动回避测试的认知效应。监测了挑战剂量的氟哌啶醇(1mg/kg ip)的作用,以观察 D 受体的任何脱敏或超敏现象。我们发现,在所有剂量下,运动活动和认知表现均增加,并且在药物给药 13 天后,敏化效应更为明显,高剂量比低剂量和中剂量更为明显。在所有接受治疗的大鼠中,氟哌啶醇的挑战剂量会减弱在熟悉和新颖环境中的运动活动,并损害水迷宫和被动回避测试中的认知。然而,在接受哌甲酯和莫达非尼治疗后,高剂量治疗大鼠的氟哌啶醇的作用比低剂量和中剂量治疗大鼠的作用略大。在接受哌甲酯治疗的大鼠中,氟哌啶醇的反应增加可以用 D 受体的超敏现象来解释,在高剂量治疗大鼠中,这种超敏现象更为明显。研究结果表明,D 受体在长期给予精神兴奋剂后引起的副作用(如行为敏化和认知耐受)方面的作用非常重要,有助于理解精神兴奋剂不良作用的机制。

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