Abstract

Despite vast literature on catecholaminergic neuromodulation of auditory cortex functioning in general, knowledge about its role for long‐term memory formation is scarce. Our previous pharmacological studies on cortex‐dependent frequency‐modulated tone‐sweep discrimination learning of Mongolian gerbils showed that auditory‐cortical D1/5‐dopamine receptor activity facilitates memory consolidation and anterograde memory formation. Considering overlapping functions of D1/5‐dopamine receptors and β‐adrenoceptors, we hypothesised a role of β‐adrenergic signalling in the auditory cortex for sweep discrimination learning and memory. Supporting this hypothesis, the β1/2‐adrenoceptor antagonist propranolol bilaterally applied to the gerbil auditory cortex after task acquisition prevented the discrimination increment that was normally monitored 1 day later. The increment in the total number of hurdle crossings performed in response to the sweeps per se was normal. Propranolol infusion after the seventh training session suppressed the previously established sweep discrimination. The suppressive effect required antagonist injection in a narrow post‐session time window. When applied to the auditory cortex 1 day before initial conditioning, β1‐adrenoceptor‐antagonising and β1‐adrenoceptor‐stimulating agents retarded and facilitated, respectively, sweep discrimination learning, whereas β2‐selective drugs were ineffective. In contrast, single‐sweep detection learning was normal after propranolol infusion. By immunohistochemistry, β1‐ and β2‐adrenoceptors were identified on the neuropil and somata of pyramidal and non‐pyramidal neurons of the gerbil auditory cortex. The present findings suggest that β‐adrenergic signalling in the auditory cortex has task‐related importance for discrimination learning of complex sounds: as previously shown for D1/5‐dopamine receptor signalling, β‐adrenoceptor activity supports long‐term memory consolidation and reconsolidation; additionally, tonic input through β1‐adrenoceptors may control mechanisms permissive for memory acquisition.

Highlights

  • The β1/2‐adrenoceptor antagonist propranolol locally applied shortly after task acquisition impaired the discrimination 1 day later compared to vehicle controls

  • frequency‐modulated tone (FM) detection‐conditioned active avoidance learning was normal after propranolol infusion

  • The discrimination rate of the antagonist‐treated group decreased on average between the last trial block of session 1 and the first trial block of session 2, while that of the control group increased. These findings strongly suggest that propranolol applied to the auditory cortex during the post‐acquisition phase antagonises actions of endogenous noradrenaline released in response to learning to enable memory storage and improvement over time, that is, memory consolidation (McGaugh, 2000)

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Summary

| INTRODUCTION

Post‐acquisition consolidation processes are relevant for the stabilisation and subsequent retrieval of long‐term memory (Dudai, Karni, & Born, 2015; Izquierdo et al, 2006; Kandel, Dudai, & Mayford, 2014; Korte & Schmitz, 2016; Matthies, 1989; McGaugh, 2000; Morris, 2006; Poo et al, 2016; Sara, 2017; Squire, Genzel, Wixted, & Morris, 2015). As recently shown for several learning tasks involving hippocampal and cortical brain regions, dopamine signalling by D1/5‐receptors and noradrenaline signalling by β‐receptors may independently modulate memory consolidation (Cavalcante et al, 2017; Moncada, 2017; Moncada et al, 2011; Ouyang, Young, Lestini, Schutsky, & Thomas, 2012). Based on these considerations, we hypothesised a.

| MATERIALS AND METHODS
| RESULTS
| DISCUSSION
Findings
DATA ACCESSIBILITY

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