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大麻二酚可减弱甲基苯丙胺诱导的条件性位置偏爱消退后的维持和复燃。

Cannabidiol attenuated the maintenance and reinstatement of extinguished methylphenidate-induced conditioned place preference in rats.

机构信息

Laboratory of Neuroscience and Behavior, Department of Physiological Sciences, University of Brasilia, Brasília, Brazil; Neuroscience Research Center, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran; Research Center of Physiology, Semnan University of Medical Sciences, Semnan, Iran.

Laboratory of Neuroscience and Behavior, University CEUMA, São Luís, Maranhão, Brazil.

出版信息

Brain Res Bull. 2021 Jan;166:118-127. doi: 10.1016/j.brainresbull.2020.11.021. Epub 2020 Nov 29.

Abstract

Methylphenidate (MPH) is a mild CNS stimulant that has been used in hyperactive children, and patients with neurodegenerative and major depressive disorders. Exposure to MPH-associated cues enhances craving and arousal in drug users. On the other hand, cannabidiol (CBD) has antipsychotic potential that might be useful in alleviating symptoms of drug addiction. The aim of this study was to investigate the effect of CBD administration on extinction and reinstatement of MPH-induced conditioning place preference (CPP) in rats. Male rats received MPH (1, 2.5 or 5 mg/kg, i.p) or morphine (5 or 10 mg/kg, s.c.) during the conditioning phase. Following the establishment of CPP, during extinction training, 60 min prior to every CPP session, animals were given daily ICV CBD (10 or 50 μg/5 μL), vehicle alone (DMSO) 10 % or were treatment-naïve. On the reinstatement day animals after receiving the initial dose of MPH, 0.5 mg/kg, and were placed into the CPP box to evaluate the CPP scoring for 10-min. Our findings indicated that morphine (5 and 10 mg/kg; s.c.) and MPH (1 and 2.5 mg/kg; i.p.) induced a CPP. The ICV administration of both doses of CBD (10 and 50 μg/5 μL) prevented the reinstatement of MPH-induced CPP, which displayed shorter extinction latency compared to treatment-naïve or DMSO 10 % groups. Therefore, CBD's site of action is a potential target for reducing the risk of MPH relapse; however, more investigation is required.

摘要

哌醋甲酯(MPH)是一种温和的中枢神经系统兴奋剂,已被用于治疗多动症儿童和神经退行性疾病和重度抑郁症患者。接触与 MPH 相关的线索会增强药物使用者的渴望和觉醒。另一方面,大麻二酚(CBD)具有抗精神病作用,可能有助于缓解药物成瘾症状。本研究旨在探讨 CBD 给药对大鼠 MPH 诱导的条件性位置偏爱(CPP)的消退和复燃的影响。雄性大鼠在条件作用阶段接受 MPH(1、2.5 或 5mg/kg,ip)或吗啡(5 或 10mg/kg,sc)。在 CPP 建立后,在消退训练期间,每节 CPP 课前 60 分钟,动物接受每日 ICV CBD(10 或 50μg/5μL)、载体(DMSO)10%或治疗前。在复燃日,动物在接受初始 MPH 剂量(0.5mg/kg)后被放入 CPP 箱,以评估 10 分钟的 CPP 评分。我们的研究结果表明,吗啡(5 和 10mg/kg;sc)和 MPH(1 和 2.5mg/kg;ip)诱导 CPP。两种剂量的 CBD(10 和 50μg/5μL)的 ICV 给药可预防 MPH 诱导的 CPP 复燃,与治疗前或 DMSO 10%组相比,CPP 消退潜伏期更短。因此,CBD 的作用部位可能是降低 MPH 复发风险的潜在靶点;然而,还需要进一步的研究。

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