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腹侧 CA1 区谷氨酸能投射至边缘下皮层在情境诱导海洛因觅药行为复发中的作用

Role of Glutamatergic Projections from the Ventral CA1 to Infralimbic Cortex in Context-Induced Reinstatement of Heroin Seeking.

机构信息

Department of Neurobiology, School of Basic Medical Sciences, Key Laboratory for Neuroscience of the Ministry of Education and National Health and Family Planning Commission, Neuroscience Research Institute, Peking University, Beijing, China.

出版信息

Neuropsychopharmacology. 2018 May;43(6):1373-1384. doi: 10.1038/npp.2017.279. Epub 2017 Nov 14.

Abstract

The prelimbic cortex (PL) and infralimbic cortex (IL) play a role in context-induced reinstatement of heroin seeking in an animal model of drug relapse. Both the PL and IL receive direct glutamatergic projections from the ventral CA1 (vCA1), which is also involved in context-induced reinstatement of cocaine and heroin seeking. Here we studied the role of vCA1-PL and vCA1-IL projections in context-induced reinstatement of heroin seeking by using electrophysiological, neuropharmacological, chemogenetic, and molecular methods. We showed that context-induced reinstatement of heroin seeking caused selective activation of the vCA1-IL but not vCA1-PL glutamatergic projections, decreased synaptosomal GluA2 expression in the IL, impaired basal synaptic transmission, and facilitation of long-term depression (LTD) in the vCA1-IL pathway. Additionally, chemogenetic inactivation of the vCA1-IL but not vCA1-PL pathway decreased context-induced reinstatement of heroin seeking. Inactivation of the vCA1-IL pathway also reversed synaptosomal GluA2 downregulation and basal transmission reduction, and blocked LTD induction. Taken together, our results demonstrate a critical role of the vCA1-IL glutamatergic projection in context-induced reinstatement of heroin seeking in a rat model of drug relapse.

摘要

前额皮质(PL)和下边缘皮质(IL)在动物药物复吸模型中发挥作用,可引发情境诱导的海洛因觅药行为重现。PL 和 IL 均接收来自腹侧 CA1(vCA1)的直接谷氨酸能投射,vCA1 也参与可卡因和海洛因觅药的情境诱导重现。在此,我们使用电生理学、神经药理学、化学遗传学和分子方法研究了 vCA1-PL 和 vCA1-IL 投射在海洛因觅药情境诱导重现中的作用。结果表明,海洛因觅药情境诱导重现选择性激活 vCA1-IL 但不激活 vCA1-PL 谷氨酸能投射,降低 IL 中突触体 GluA2 的表达,损害 IL 中的基础突触传递,并促进 vCA1-IL 通路中的长时程抑制(LTD)。此外,vCA1-IL 通路的化学遗传失活降低了海洛因觅药的情境诱导重现。vCA1-IL 通路的失活还逆转了突触体 GluA2 下调和基础传递减少,并阻断了 LTD 的诱导。总之,我们的研究结果表明,vCA1-IL 谷氨酸能投射在大鼠药物复吸模型中海洛因觅药的情境诱导重现中起关键作用。

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