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腹侧苍白球谷氨酸能厌恶网络编码对可卡因的戒断和再次接触。

A ventral pallidal glutamatergic aversive network encodes abstinence from and reexposure to cocaine.

作者信息

Levi Liran A, Inbar Kineret, Tseiger Esti, Kupchik Yonatan M

机构信息

Department of Medical Neurobiology, Institute for Medical Research Israel-Canada (IMRIC), Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.

IMRIC Center for Addiction Research (ICARe), The Hebrew University of Jerusalem, Jerusalem, Israel.

出版信息

Sci Adv. 2025 Jul 25;11(30):eadu6074. doi: 10.1126/sciadv.adu6074.

Abstract

Relapse to drugs of abuse can occur after long periods of abstinence. The ventral pallidum (VP) is central to drug addiction, and its glutamatergic neurons (VP), whose activation drives aversion, inhibit drug seeking. However, it remains unknown whether these neurons encode the abstinence from and relapse to drugs. We show here that VP projections specifically to the aversion-related lateral habenula (LHb) and ventral tegmental area gabaergic (VTA) neurons show plasticity induced by abstinence from and reexposure to cocaine or cocaine cues. Both these pathways potentiate during abstinence and restore baseline values upon drug reexposure but with different plasticity mechanisms. Last, inhibiting the VP → LHb pathway enhances cocaine preference after abstinence, while inhibiting the VP → VTA pathway shows variable effects. These findings establish an aversive circuit orchestrated by VP neurons encoding long-term abstinence-driven changes that may contribute to drug relapse.

摘要

长期禁欲后仍可能出现药物滥用复发的情况。腹侧苍白球(VP)在药物成瘾中起核心作用,其谷氨酸能神经元(VP)的激活会引发厌恶情绪,从而抑制觅药行为。然而,这些神经元是否编码对药物的禁欲和复发情况仍不清楚。我们在此表明,VP向与厌恶相关的外侧缰核(LHb)和腹侧被盖区γ-氨基丁酸能(VTA)神经元的特异性投射显示出因禁欲和重新接触可卡因或可卡因线索而诱导的可塑性。这两条通路在禁欲期间均增强,在重新接触药物后恢复到基线值,但可塑性机制不同。最后,抑制VP→LHb通路会增强禁欲后的可卡因偏好,而抑制VP→VTA通路则显示出不同的效果。这些发现建立了一个由VP神经元精心编排的厌恶回路,该回路编码长期禁欲驱动的变化,这可能导致药物复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a29e/12285697/6a49cd5480bc/sciadv.adu6074-f1.jpg

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