Abstract

The hippocampus and striatum guide place-strategy and response-strategy learning, respectively, and they have dissociable roles in memory systems, which could compensate in case of temporary or permanent damage. Although acute alcohol (AA) treatment had been shown to have adverse effects on hippocampal function, whether it causes the functional compensation and the underlying mechanisms is unknown. In this study, rats treated with a low dose of AA avoided a hippocampus-dependent spatial strategy, instead preferring a striatum-dependent response strategy. Consistently, the learning-induced increase in hippocampal, but not striatal, pCREB was rendered less pronounced due to diminished activity of pPKA, but not pERK or pCaMKII. As rats approached the turn-decision area, Sp-cAMP, a PKA activator, was found to mitigate the inhibitory effect of AA on intra- and cross-structure synchronized neuronal oscillations, and rescue response-strategy bias and spatial learning deficits. Our study provides strong evidence of the critical link between neural couplings and strategy selection. Moreover, the PKA/CREB-signaling pathway is involved in the suppressive effect of AA on neural correlates of place-learning strategy. The novel important evidence provided here shows the functional couplings between the hippocampus and striatum in spatial learning processing and suggests possible avenues for therapeutic intervention.

Highlights

  • Our memory is composed of multiple anatomically and functionally distinct systems (Squire and Zola, 1996)

  • Acute alcohol was i.p. injected to well-trained rats at either 1.0 g/kg (AA-1.0) or 2.0 g/kg (AA-2.0) dose 30 min before behavioral task

  • Our behavioral experiment demonstrates that acute alcohol (AA) exposure before the learning session attenuates the use of the HPC-dependent spatial strategy and causes a switch to a response strategy that relies on the dorsal striatum (DS) to locate the food reward in the T-maze task

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Summary

Introduction

Our memory is composed of multiple anatomically and functionally distinct systems (Squire and Zola, 1996). Previous studies with animal models have provided compelling evidence that alcohol can attenuate spatial memory mediated by the hippocampus with much greater potency than it attenuates learning, which is known to be mediated by other neural systems. Ethanol produces a shift in bias from the use of spatial information to non-spatial information to solve learning and memory tasks (Matthews et al, 1999). These findings clearly indicate that alcohol can disturb hippocampus-dependent “place” strategies but not “response” strategies. The neural mechanism underlying this alcohol-induced modification of multiple memory systems, remains elusive

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