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Stress augments the rewarding memory of cocaine via the activation of brainstem-reward circuitry
https://doi.org/10.24517/00050519
https://doi.org/10.24517/00050519be0933ff-0197-4693-b69a-0f6a9d25a8a6
名前 / ファイル | ライセンス | アクション |
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Item type | 学術雑誌論文 / Journal Article(1) | |||||||
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公開日 | 2019-05-10 | |||||||
タイトル | ||||||||
タイトル | Stress augments the rewarding memory of cocaine via the activation of brainstem-reward circuitry | |||||||
言語 | ||||||||
言語 | eng | |||||||
資源タイプ | ||||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||||
資源タイプ | journal article | |||||||
ID登録 | ||||||||
ID登録 | 10.24517/00050519 | |||||||
ID登録タイプ | JaLC | |||||||
著者 |
Shinohara, Fumiya
× Shinohara, Fumiya× Asaoka, Yuta× Kamii, Hironori× Minami, Masabumi× Kaneda, Katsuyuki |
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著者別表示 |
金田, 勝幸
× 金田, 勝幸
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提供者所属 | ||||||||
内容記述タイプ | Other | |||||||
内容記述 | 金沢大学医薬保健研究域薬学系 | |||||||
書誌情報 |
Addiction Biology 巻 24, 号 3, p. 509-521, 発行日 2019-05-01 |
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ISSN | ||||||||
収録物識別子タイプ | ISSN | |||||||
収録物識別子 | 1355-6215 | |||||||
NCID | ||||||||
収録物識別子タイプ | NCID | |||||||
収録物識別子 | AA11053387 | |||||||
DOI | ||||||||
関連タイプ | isVersionOf | |||||||
識別子タイプ | DOI | |||||||
関連識別子 | 10.1111/adb.12617 | |||||||
出版者 | ||||||||
出版者 | Blackwell Publishing Ltd | |||||||
抄録 | ||||||||
内容記述タイプ | Abstract | |||||||
内容記述 | Effects of stress on the reward system are well established in the literature. Although previous studies have revealed that stress can reinstate extinguished addictive behaviors related to cocaine, the effects of stress on the rewarding memory of cocaine are not fully understood. Here, we provide evidence that stress potentiates the expression of rewarding memory of cocaine via the activation of brainstem-reward circuitry using a cocaine-induced conditioned place preference (CPP) paradigm combined with restraint stress in rats. The rats exposed to 30-minute restraint stress immediately before posttest exhibited significantly larger CPP scores compared with non-stressed rats. Intra-laterodorsal tegmental nucleus (LDT) microinjection of a β or α2 adrenoceptor antagonist attenuated the stress-induced enhancement of cocaine CPP. Consistent with this observation, intra-LDT microinjection of a β or α2 adrenoceptor agonist before posttest increased cocaine CPP. Additionally, intra-ventral tegmental area (VTA) microinjection of antagonists for the muscarinic acetylcholine, nicotinic acetylcholine or glutamate receptors attenuated the stress-induced enhancement of cocaine CPP. Finally, intra-medial prefrontal cortex (mPFC) microinjection of a D1 receptor antagonist also reduced the stress-induced enhancement of cocaine CPP. These findings suggest a mechanism wherein the LDT is activated by noradrenergic input from the locus coeruleus, leading to the activation of VTA dopamine neurons via both cholinergic and glutamatergic transmission and the subsequent excitation of the mPFC to enhance the memory of cocaine-induced reward value. © 2018 Society for the Study of Addiction. | |||||||
内容記述 | ||||||||
内容記述タイプ | Other | |||||||
内容記述 | Embargo Period 12 months | |||||||
権利 | ||||||||
権利情報 | Copyright © 2018 Society for the Study of Addiction | |||||||
著者版フラグ | ||||||||
出版タイプ | AM | |||||||
出版タイプResource | http://purl.org/coar/version/c_ab4af688f83e57aa |