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可卡因自我给药和戒断调节大鼠伏隔核 NMDA 受体亚单位和活性区蛋白。

Cocaine Self-Administration and Abstinence Modulate NMDA Receptor Subunits and Active Zone Proteins in the Rat Nucleus Accumbens.

机构信息

Maj Institute of Pharmacology Polish Academy of Sciences, Department of Drug Addiction Pharmacology, Smętna 12, PL 31-343 Kraków, Poland.

Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Via Balzaretti 9, 20133 Milano, Italy.

出版信息

Molecules. 2020 Jul 31;25(15):3480. doi: 10.3390/molecules25153480.

Abstract

Cocaine-induced plasticity in the glutamatergic transmission and its -methyl-d-aspartate (NMDA) receptors are critically involved in the development of substance use disorder. The presynaptic active zone proteins control structural synaptic plasticity; however, we are still far from understanding the molecular determinants important for cocaine seeking behavior. The aim of this study was to investigate the effect of cocaine self-administration and different conditions of cocaine forced abstinence on the composition of the NMDA receptor subunits and on the levels of active zone proteins, i.e., Ras-related protein 3A (Rab3A), Rab3 interacting molecules 1 (RIM1) and mammalian uncoordinated protein 13 (Munc13) in the rat nucleus accumbens. We found an up-regulation of the accumbal levels of GluN1 and GluN2A following cocaine self-administration that was paralleled by an increase of Munc13 and RIM1 levels. At the same time, we also demonstrated that different conditions of cocaine abstinence abolished changes in NMDA receptor subunits (except for higher GluN1 levels after cocaine abstinence with extinction training), while an increase in the Munc13 concentration was shown in rats housed in an enriched environment. In conclusion, cocaine self-administration is associated with the specific up-regulation of the NMDA receptor subunit composition and is related with new presynaptic targets controlling neurotransmitter release. Moreover, changes observed in cocaine abstinence with extinction training and in an enriched environment in the levels of NMDA receptor subunit and in the active zone protein, respectively, may represent a potential regulatory step in cocaine-seeking behavior.

摘要

可卡因诱导的谷氨酸能传递和 -甲基-D-天冬氨酸(NMDA)受体的可塑性在物质使用障碍的发展中起着关键作用。突触前活性区蛋白控制结构突触可塑性;然而,我们仍然远未了解对可卡因寻求行为重要的分子决定因素。本研究旨在探讨可卡因自我给药和不同可卡因强制戒断条件对 NMDA 受体亚基组成以及活性区蛋白水平(即 Ras 相关蛋白 3A(Rab3A)、Rab3 相互作用分子 1(RIM1)和哺乳动物不协调蛋白 13(Munc13))的影响在大鼠伏隔核中。我们发现可卡因自我给药后,伏隔核中 GluN1 和 GluN2A 的水平上调,同时 Munc13 和 RIM1 的水平也增加。与此同时,我们还证明,不同的可卡因戒断条件消除了 NMDA 受体亚基的变化(除了可卡因戒断后伴有消退训练时 GluN1 水平升高),而在丰富环境中饲养的大鼠中,Munc13 浓度增加。总之,可卡因自我给药与 NMDA 受体亚基组成的特异性上调有关,与控制神经递质释放的新的突触前靶点有关。此外,分别在可卡因戒断伴消退训练和丰富环境中观察到的 NMDA 受体亚基和活性区蛋白水平的变化,可能代表可卡因寻求行为的潜在调节步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e09/7436251/9161c38b2131/molecules-25-03480-g001.jpg

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