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单次可卡因暴露通过增强小鼠直接纹状体通路神经元的活性来损害强化学习。

Single Exposure to Cocaine Impairs Reinforcement Learning by Potentiating the Activity of Neurons in the Direct Striatal Pathway in Mice.

机构信息

Key Laboratory of Modern Teaching Technology, Ministry of Education, Shaanxi Normal University, Xi'an, 710062, China.

College of Life Sciences, Shaanxi Normal University, Xi'an, 710119, China.

出版信息

Neurosci Bull. 2021 Aug;37(8):1119-1134. doi: 10.1007/s12264-021-00687-8. Epub 2021 Apr 27.

DOI:10.1007/s12264-021-00687-8
PMID:33905097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8353048/
Abstract

Plasticity in the glutamatergic synapses on striatal medium spiny neurons (MSNs) is not only essential for behavioral adaptation but also extremely vulnerable to drugs of abuse. Modulation on these synapses by even a single exposure to an addictive drug may interfere with the plasticity required by behavioral learning and thus produce impairment. In the present work, we found that the negative reinforcement learning, escaping mild foot-shocks by correct nose-poking, was impaired by a single in vivo exposure to 20 mg/kg cocaine 24 h before the learning in mice. Either a single exposure to cocaine or reinforcement learning potentiates the glutamatergic synapses on MSNs expressing the striatal dopamine 1 (D1) receptor (D1-MSNs). However, 24 h after the cocaine exposure, the potentiation required for reinforcement learning was disrupted. Specific manipulation of the activity of striatal D1-MSNs in D1-cre mice demonstrated that activation of these MSNs impaired reinforcement learning in normal D1-cre mice, but inhibition of these neurons reversed the reinforcement learning impairment induced by cocaine. The results suggest that cocaine potentiates the activity of direct pathway neurons in the dorsomedial striatum and this potentiation might disrupt the potentiation produced during and required for reinforcement learning.

摘要

纹状体中间神经元(MSNs)上谷氨酸能突触的可塑性不仅对行为适应至关重要,而且极易受到滥用药物的影响。即使是单次接触成瘾药物对这些突触的调制也可能干扰行为学习所需的可塑性,从而导致损伤。在本工作中,我们发现,在学习前 24 小时内,单次体内给予 20mg/kg 可卡因暴露,会损害表达纹状体多巴胺 1 受体(D1-MSNs)的 MSNs 上的负强化学习,即通过正确的鼻触逃避轻度足底电击。可卡因暴露或强化学习均可增强表达纹状体多巴胺 1 受体(D1-MSNs)的 MSNs 上的谷氨酸能突触。然而,在可卡因暴露 24 小时后,强化学习所需的增强作用被破坏。在 D1-cre 小鼠中对纹状体 D1-MSNs 活性的特定操纵表明,这些 MSNs 的激活会损害正常 D1-cre 小鼠的强化学习,但抑制这些神经元可逆转可卡因引起的强化学习损伤。结果表明,可卡因增强了背内侧纹状体中直接通路神经元的活性,这种增强可能会破坏强化学习过程中产生的增强作用。