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齿状回中D1样多巴胺受体介导大麻二酚促进消退以及预防甲基苯丙胺诱导的条件性位置偏爱中的复吸。

D1-like dopamine receptors in the dentate gyrus mediate cannabidiol's facilitation of extinction and prevention of reinstatement in methamphetamine-induced conditioned place preference.

作者信息

Danesh Elaheh, Saghafi Mohammad, Mozafari Roghayeh, Mesgar Somaye, Haghparast Abbas

机构信息

Neuroscience Research Center, Institute of Neuroscience and Cognition, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Pharmacology and Toxicology Department, Faculty of Pharmacy and Pharmaceutical Sciences, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.

出版信息

Pharmacol Biochem Behav. 2025 Nov;256:174094. doi: 10.1016/j.pbb.2025.174094. Epub 2025 Sep 4.

Abstract

Methamphetamine (METH) is a highly addictive psychostimulant, and despite its widespread abuse, there are no FDA-approved treatments for METH use disorder (MUD). Cannabidiol (CBD), a non-psychoactive cannabinoid, has shown promise in reducing behaviors linked to psychostimulant use, including METH. However, the underlying neurobiological mechanisms remain unclear. Emerging evidence suggests that CBD may act on the dopamine system to influence drug-seeking behavior. D1-like dopamine receptors (D1Rs) in the hippocampus (HPC) are involved in memory processes related to rewards, which may contribute to CBD's effects. This study examined whether D1Rs in the dentate gyrus (DG) region of the HPC play a role in CBD's modulation of METH-induced conditioned place preference (CPP) during extinction and reinstatement. Adult male Wistar rats received the D1Rs antagonist SCH23390 (0.25, 1, and 4 μg/0.5 μl saline) into the DG region before intracerebroventricular injection of CBD (10 and 50 μg/5 μl of 12 % DMSO). Results show that the highest dose of SCH23390 (4 μg) significantly blocked CBD's ability to enhance extinction of METH-CPP. Moreover, SCH23390 (1 and 4 μg) reversed CBD's prevention of reinstatement of METH-CPP. These findings suggest that D1Rs in the DG region are involved in mediating CBD's effects and offer insights into its therapeutic potential for MUD.

摘要

甲基苯丙胺(METH)是一种极易成瘾的精神兴奋剂,尽管其滥用现象普遍,但美国食品药品监督管理局(FDA)尚未批准用于治疗甲基苯丙胺使用障碍(MUD)的药物。大麻二酚(CBD)是一种无精神活性的大麻素,已显示出在减少与精神兴奋剂使用相关行为(包括甲基苯丙胺)方面的前景。然而,其潜在的神经生物学机制仍不清楚。新出现的证据表明,CBD可能作用于多巴胺系统以影响觅药行为。海马体(HPC)中的D1样多巴胺受体(D1Rs)参与与奖励相关的记忆过程,这可能有助于CBD发挥作用。本研究探讨了海马体齿状回(DG)区域中的D1Rs在消退和恢复过程中是否参与CBD对甲基苯丙胺诱导的条件性位置偏爱(CPP)的调节作用。成年雄性Wistar大鼠在脑室内注射CBD(10和50μg/5μl的12%二甲基亚砜)之前,将D1Rs拮抗剂SCH23390(0.25、1和4μg/0.5μl生理盐水)注射到DG区域。结果表明,SCH23390的最高剂量(4μg)显著阻断了CBD增强甲基苯丙胺-CPP消退的能力。此外,SCH23390(1和4μg)逆转了CBD对甲基苯丙胺-CPP恢复的预防作用。这些发现表明,DG区域中的D1Rs参与介导CBD的作用,并为其对MUD的治疗潜力提供了见解。

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