Suppr超能文献

托吡酯增强了可卡因对年轻成年小鼠的奖赏效应,限制了其临床应用价值。

Topiramate increases the rewarding properties of cocaine in young-adult mice limiting its clinical usefulness.

作者信息

Arenas M C, Mateos-García A, Manzanedo C, Rodríguez-Arias M, Aguilar M A, Navarrete F, Gutiérrez M S García, Manzanares J, Miñarro J

机构信息

Unidad de Investigación Psicobiología de las Drogodependencias, Departamento de Psicobiología, Facultad de Psicología, Universitat de València, Avda. Blasco Ibañez, 21, 46010, Valencia, Spain.

Red Temática de Investigación Cooperativa en Salud (RETICS-Trastornos Adictivos), Instituto de Salud Carlos III, MICINN and FEDER, Madrid, Spain.

出版信息

Psychopharmacology (Berl). 2016 Dec;233(23-24):3849-3859. doi: 10.1007/s00213-016-4409-4. Epub 2016 Sep 5.

Abstract

RATIONALE

Topiramate is an anticonvulsant drug which has been evaluated as a therapeutic option for the treatment of cocaine addiction during the last decade.

OBJECTIVES

The purpose of this study was to evaluate the effects of topiramate on the reinforcing actions of cocaine. To this aim, the topiramate-mediated regulation of acquisition and extinction phases of the cocaine conditioned place preference (CPP) was assessed in young-adult mice using three experimental designs.

METHODS

Topiramate (50 mg/kg, p.o.) was given as follows: (1) during cocaine (1 and 25 mg/kg, i.p.) conditioning sessions (4 days) and cocaine (25 mg/kg) post-conditioning session; (2) 2 weeks before and during cocaine conditioning (25 mg/kg); and (3) during extinction of CPP induced by cocaine (25 mg/kg). In the first experimental design, changes in tyrosine hydroxylase (TH) and dopamine transporter (DAT) gene expressions were measured in the ventral tegmental area (VTA).

RESULTS

Topiramate significantly increased cocaine-induced CPP and delayed or failed to produce extinction after the first cocaine reinstatement extinction in the first and second experiments. Furthermore, treatment with topiramate after place conditioning blocked the extinction of cocaine-induced CPP. TH and DAT gene expression in the VTA was significantly lower both with topiramate alone and in combination with cocaine compared with animals receiving only cocaine.

CONCLUSIONS

These findings suggest that topiramate increases the rewarding properties of cocaine, at least in part, by regulating dopaminergic signaling in the mesolimbic circuit. Consequently, the results of this study do not support the use of topiramate for the treatment of problems related to cocaine dependence.

HIGHLIGHTS

• Topiramate increases the rewarding properties of cocaine in CPP • Topiramate alters dopaminergic signaling in the mesolimbic circuit • Topiramate delays the extinction of cocaine-induced CPP • TH and DAT gene expression in the VTA decreases with topiramate and/or with cocaine • Results show that it should limit the use of topiramate in cocaine-dependent subjects.

摘要

原理

托吡酯是一种抗惊厥药物,在过去十年中已被评估为治疗可卡因成瘾的一种治疗选择。

目的

本研究的目的是评估托吡酯对可卡因强化作用的影响。为了实现这一目标,使用三种实验设计在年轻成年小鼠中评估了托吡酯介导的可卡因条件性位置偏爱(CPP)获得和消退阶段的调节。

方法

托吡酯(50mg/kg,口服)给药方式如下:(1)在可卡因(1和25mg/kg,腹腔注射)条件训练阶段(4天)和可卡因(25mg/kg)条件训练后阶段;(2)在可卡因(25mg/kg)条件训练前2周和训练期间;(3)在可卡因(25mg/kg)诱导的CPP消退期间。在第一个实验设计中,测量腹侧被盖区(VTA)中酪氨酸羟化酶(TH)和多巴胺转运体(DAT)基因表达的变化。

结果

在第一个和第二个实验中,托吡酯显著增加了可卡因诱导的CPP,并在首次可卡因复吸消退后延迟或未能产生消退。此外,位置条件训练后给予托吡酯治疗可阻断可卡因诱导的CPP的消退。与仅接受可卡因的动物相比,单独使用托吡酯以及与可卡因联合使用时,VTA中的TH和DAT基因表达均显著降低。

结论

这些发现表明,托吡酯至少部分地通过调节中脑边缘回路中的多巴胺能信号来增加可卡因的奖赏特性。因此,本研究结果不支持使用托吡酯治疗与可卡因依赖相关的问题。

要点

•托吡酯增加了CPP中可卡因的奖赏特性 •托吡酯改变了中脑边缘回路中的多巴胺能信号 •托吡酯延迟了可卡因诱导的CPP的消退 •托吡酯和/或可卡因使VTA中的TH和DAT基因表达降低 •结果表明应限制托吡酯在可卡因依赖者中的使用

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验