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大鼠伏隔核中ASIC1A的过表达增强了觅可卡因行为。

Overexpression of ASIC1A in the nucleus accumbens of rats potentiates cocaine-seeking behavior.

作者信息

Gutman Andrea L, Cosme Caitlin V, Noterman Maria F, Worth Wensday R, Wemmie John A, LaLumiere Ryan T

机构信息

Department of Psychological and Brain Sciences, University of Iowa, Iowa City, IA, USA.

Interdisciplinary Graduate Program in Neuroscience, University of Iowa, Iowa City, IA, USA.

出版信息

Addict Biol. 2020 Mar;25(2):e12690. doi: 10.1111/adb.12690. Epub 2018 Nov 6.

DOI:10.1111/adb.12690
PMID:30397978
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9092352/
Abstract

Acid-sensing ion channels (ASICs) are abundantly expressed in the nucleus accumbens core (NAcore), a region of the mesolimbocortical system that has an established role in regulating drug-seeking behavior. Previous work shows that a single dose of cocaine reduced the AMPA-to-NMDA ratio in Asic1a mice, an effect observed after withdrawal in wild-type mice, whereas ASIC1A overexpression in the NAcore of rats decreases cocaine self-administration. However, whether ASIC1A overexpression in the NAcore alters measures of drug-seeking behavior after the self-administration period is unknown. To examine this issue, the ASIC1A subunit was overexpressed in male Sprague-Dawley rats by injecting them with adeno-associated virus, targeted at the NAcore, after completion of 2 weeks of cocaine or food self-administration. After 21 days of homecage abstinence, rats underwent a cue-/context-driven drug/food-seeking test, followed by extinction training and then drug/food-primed, cued, and cued + drug/food-primed reinstatement tests. The results indicate that ASIC1A overexpression in the NAcore enhanced cue-/context-driven cocaine seeking, cocaine-primed reinstatement, and cued + cocaine-primed reinstatement but had no effect on food-seeking behavior, indicating a selective effect for ASIC1A in the processes underlying extinction and cocaine-seeking behavior.

摘要

酸敏感离子通道(ASICs)在伏隔核核心区(NAcore)大量表达,伏隔核核心区是中脑边缘皮质系统的一个区域,在调节觅药行为方面具有既定作用。先前的研究表明,单剂量可卡因降低了Asic1a小鼠中的AMPA与NMDA的比率,这种效应在野生型小鼠戒断后也能观察到,而在大鼠伏隔核核心区过表达ASIC1A会减少可卡因的自我给药。然而,伏隔核核心区过表达ASIC1A是否会改变自我给药期后觅药行为的指标尚不清楚。为了研究这个问题,在雄性Sprague-Dawley大鼠完成2周的可卡因或食物自我给药后,通过向其注射靶向伏隔核核心区的腺相关病毒,使ASIC1A亚基过表达。在21天的笼内戒断后,大鼠接受线索/情境驱动的药物/食物觅求测试,随后进行消退训练,然后进行药物/食物启动、线索和线索+药物/食物启动的复吸测试。结果表明,伏隔核核心区ASIC1A过表达增强了线索/情境驱动的可卡因觅求、可卡因启动的复吸以及线索+可卡因启动的复吸,但对食物觅求行为没有影响,表明ASIC1A在消退和可卡因觅求行为背后的过程中具有选择性作用。

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