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亚甲二氧基吡咯戊酮(MDPV)损害工作记忆,并改变中脑边缘多巴胺信号传递模式。

Methylenedioxypyrovalerone (MDPV) impairs working memory and alters patterns of dopamine signaling in mesocorticolimbic substrates.

机构信息

Department of Pathology and Laboratory Medicine, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.

Center for Substance Abuse Research, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.

出版信息

Neurosci Res. 2020 Jun;155:56-62. doi: 10.1016/j.neures.2019.07.003. Epub 2019 Jul 11.

Abstract

Knowledge remains limited about how chronic cathinone exposure impacts dopamine systems in brain reward circuits. In the present study, a binge-like MDPV exposure that impaired novel object recognition (NOR) dysregulated dopamine markers in mesocorticolimbic substrates of rats, with especially profound effects on D1 and D2 receptor's and VMAT gene expression. Our data suggested that dopamine receptivity was reduced in the NAc but increased in the PFC and dopamine-producing VTA. The MDPV-induced impairment of NOR was prevented by a D1 receptor antagonist, suggesting that chronic MDPV exposure produces site-specific dysregulation of dopamine markers in the mesocorticolimbic circuit and memory deficits in the NOR test that are influenced by D1 receptors.

摘要

关于慢性去甲伪麻黄碱暴露如何影响大脑奖励回路中的多巴胺系统,人们的了解仍然有限。在本研究中,类似狂欢的 MDPV 暴露会损害大鼠中边缘皮质奖赏回路中的新物体识别(NOR),从而使多巴胺标记物失调,对 D1 和 D2 受体和 VMAT 基因表达的影响尤其明显。我们的数据表明,NAc 中的多巴胺受体反应性降低,但 PFC 和产生多巴胺的 VTA 中的多巴胺受体反应性增加。D1 受体拮抗剂可预防 MDPV 诱导的 NOR 损伤,这表明慢性 MDPV 暴露会导致中边缘皮质奖赏回路中多巴胺标记物的特定部位失调,并导致 NOR 测试中的记忆缺陷,而 D1 受体对这些缺陷有影响。

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