甲基苯丙胺诱导的斑马鱼条件位置偏好的灭绝和恢复

IF 3.1 3区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Liao-Chen Chen, Ming-Huan Chan, Hwei-Hsien Chen
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引用次数: 0

摘要

斑马鱼的条件位置偏好(CPP)范式已被用于测量药物奖励,但关于CPP恢复以确定复发脆弱性的研究有限。本研究旨在探讨甲基苯丙胺(MA)诱导的斑马鱼CPP的消失和恢复,并评估该模型的预测有效性。斑马鱼在CPP训练期间接受不同剂量的MA (0-60 mg/kg)。优选剂量为40 mg/kg的MA可通过密闭或非密闭程序消除。通过给药剂量MA (20 mg/kg)或各种应激源恢复被熄灭的CPP。为了评估持续恢复的易感性,在禁欲14天后重新测试MA CPP和恢复。此外,我们还监测了SCH23390、纳曲酮和可乐定对MA CPP在获得期、表达期和恢复期的影响。MA诱导CPP呈剂量依赖性。非受限和受限消光过程都减少了在ma配对侧花费的时间。MA、追逐应激或育亨宾的启动剂量恢复了消失的CPP。戒断14 d后,MA CPP仍处于熄灭状态,并在MA启动或追逐应激下显著恢复。与在啮齿类动物中的观察结果相似,SCH23390抑制MA CPP的获得,纳曲酮降低表达和MA启动诱导的恢复,而可乐定阻止应激诱导的MA CPP恢复。这项工作扩展了斑马鱼CPP模式,包括灭绝和恢复阶段,证明了预测的有效性,并强调了其作为探索药物复发的有价值工具的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Extinction and reinstatement of methamphetamine-induced conditioned place preference in zebrafish

Extinction and reinstatement of methamphetamine-induced conditioned place preference in zebrafish

Conditioned place preference (CPP) paradigm in zebrafish has been used to measure drug reward, but there is limited research on CPP reinstatement to determine relapse vulnerability. The present study aimed to investigate extinction and reinstatement of methamphetamine (MA)-induced CPP in zebrafish and evaluate the model's predictive validity. Zebrafish received different doses of MA (0–60 mg/kg) during CPP training. The preferred dose of MA at 40 mg/kg was used for extinction via either confined or nonconfined procedures. The extinguished CPP was reinstated by administering a priming dose of MA (20 mg/kg) or various stressors. To assess persistent susceptibility to reinstatement, MA CPP and reinstatement were retested following 14 days of abstinence. In addition, the effects of SCH23390, naltrexone, and clonidine on MA CPP during acquisition, expression, or reinstatement phases were monitored. MA induced CPP in a dose-dependent manner. Both nonconfined and confined extinction procedures time-dependently reduced the time spent on the MA-paired side. A priming dose of MA, chasing stress, or yohimbine reinstated the extinguished CPP. After 14 days of abstinence, the MA CPP remained extinguished and was significantly reinstated by MA priming or chasing stress. Similar to the observations in rodents, SCH23390 suppressed the acquisition of MA CPP, naltrexone reduced the expression and MA priming-induced reinstatement, while clonidine prevented stress-induced reinstatement of MA CPP. This work expanded the zebrafish CPP paradigm to include extinction and reinstatement phases, demonstrating predictive validity and highlighting its potential as a valuable tool for exploring drug relapse.

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来源期刊
Addiction Biology
Addiction Biology 生物-生化与分子生物学
CiteScore
8.10
自引率
2.90%
发文量
118
审稿时长
6-12 weeks
期刊介绍: Addiction Biology is focused on neuroscience contributions and it aims to advance our understanding of the action of drugs of abuse and addictive processes. Papers are accepted in both animal experimentation or clinical research. The content is geared towards behavioral, molecular, genetic, biochemical, neuro-biological and pharmacology aspects of these fields. Addiction Biology includes peer-reviewed original research reports and reviews. Addiction Biology is published on behalf of the Society for the Study of Addiction to Alcohol and other Drugs (SSA). Members of the Society for the Study of Addiction receive the Journal as part of their annual membership subscription.
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