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伏隔核内食欲素-1和-2受体在大鼠吗啡敏化形成中的作用

Role of orexin-1 and -2 receptors within the nucleus accumbens in the acquisition of sensitization to morphine in rats.

作者信息

Assar Nasim, Mahmoudi Dorna, Mousavi Zahra, Zarrabian Shahram, Haghparast Abbas

机构信息

Neuroscience Research Center, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Department of Pharmacology & Toxicology, Faculty of Pharmacy, Pharmaceutical Sciences Branch, Islamic Azad University, Tehran, Iran.

出版信息

Behav Brain Res. 2019 Nov 5;373:112090. doi: 10.1016/j.bbr.2019.112090. Epub 2019 Jul 17.

Abstract

It has been reported that orexins A and B are involved in the mediation of drug reward. In addition, the nucleus accumbens (NAc) has an important role in the development of morphine-conditioned place preference (CPP) and morphine sensitization. In the present study, we aimed to evaluate the role of orexin receptors within the NAc in morphine sensitization using CPP paradigm. Adult male Wistar rats were used and were bilaterally implanted by two cannulae in the NAc. The animals received intra-accumbal administration of OX1 or OX2 receptor antagonists, SB-334867 (0.1, 1, and 10 nM/side) or TCS OX2 29 (2, 10, and 20 nM/side), 10 min before morphine injection during the sensitization period, during which the animals received repeated administration of morphine (5 mg/kg; s.c.) once daily for three days followed by 5 morphine injection-free days. Then the CPP paradigm was conducted for the evaluation of morphine rewarding properties by injecting a sub-threshold dose of morphine (0.5 mg/kg; s.c.). The results showed that bilateral administration of OX1 receptor antagonist into the NAc reduced acquisition of morphine sensitization in a dose-dependent manner, but OX2 receptor antagonist produced similar effect only at its highest dose, indicating that OX1 and OX2 receptors within the NAc are involved in the acquisition of morphine sensitization.

摘要

据报道,食欲素A和B参与药物奖赏的介导。此外,伏隔核(NAc)在吗啡条件性位置偏爱(CPP)和吗啡敏化的形成中起重要作用。在本研究中,我们旨在使用CPP范式评估NAc内食欲素受体在吗啡敏化中的作用。使用成年雄性Wistar大鼠,通过双侧套管将其植入NAc。在敏化期,动物在注射吗啡前10分钟接受伏隔核内注射OX1或OX2受体拮抗剂,SB-334867(0.1、1和10 nM/侧)或TCS OX2 29(2、10和20 nM/侧),在此期间动物每天一次重复注射吗啡(5 mg/kg;皮下注射),持续三天,随后有5天不注射吗啡。然后通过注射阈下剂量的吗啡(0.5 mg/kg;皮下注射)进行CPP范式,以评估吗啡的奖赏特性。结果表明,向NAc双侧注射OX1受体拮抗剂以剂量依赖性方式降低了吗啡敏化的获得,但OX2受体拮抗剂仅在其最高剂量时产生类似效果,表明NAc内的OX1和OX2受体参与了吗啡敏化的获得。

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