4.6 Article

Chronic alcohol consumption shifts learning strategies and synaptic plasticity from hippocampus to striatum-dependent pathways

Journal

FRONTIERS IN PSYCHIATRY
Volume 14, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fpsyt.2023.1129030

Keywords

alcohol; learning strategies; memory systems; hippocampus (CA1); dorsal striatum; synaptic plasticity; addiction; amygdala

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This study found that chronic alcohol consumption and alcohol withdrawal modulate the use of spatial and single cue-based learning strategies, and enhance the association between addictive substances and the reward system through the activation of the amygdala. This cognitive imbalance could contribute to maintain addictive behaviors and increase the risk of relapse.
IntroductionThe hippocampus and striatum have dissociable roles in memory and are necessary for spatial and procedural/cued learning, respectively. Emotionally charged, stressful events promote the use of striatal- over hippocampus-dependent learning through the activation of the amygdala. An emerging hypothesis suggests that chronic consumption of addictive drugs similarly disrupt spatial/declarative memory while facilitating striatum-dependent associative learning. This cognitive imbalance could contribute to maintain addictive behaviors and increase the risk of relapse. MethodsWe first examined, in C57BL/6 J male mice, whether chronic alcohol consumption (CAC) and alcohol withdrawal (AW) might modulate the respective use of spatial vs. single cue-based learning strategies, using a competition protocol in the Barnes maze task. We then performed in vivo electrophysiological studies in freely moving mice to assess learning-induced synaptic plasticity in both the basolateral amygdala (BLA) to dorsal hippocampus (dCA1) and BLA to dorsolateral striatum (DLS) pathways. ResultsWe found that both CAC and early AW promote the use of cue-dependent learning strategies, and potentiate plasticity in the BLA -> DLS pathway while reducing the use of spatial memory and depressing BLA -> dCA1 neurotransmission. DiscussionThese results support the view that CAC disrupt normal hippocampo-striatal interactions, and suggest that targeting this cognitive imbalance through spatial/declarative task training could be of great help to maintain protracted abstinence in alcoholic patients.

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