Supra-normal stimulation of dopamine D1 receptors in the prelimbic cortex blocks behavioral expression of both aversive and rewarding associative memories through a cyclic-AMP-dependent signaling pathway

• Published in: Neuropharmacology 2013-04, Vol.67, p.104-114
• Main Authors: Lauzon, Nicole M., Bechard, Melanie, Ahmad, Tasha, Laviolette, Steven R.
• Format: Article
• Language: English
• Subjects: Animals; Association Learning - drug effects; Association Learning - physiology; Associative memory; Aversion; Avoidance Learning - drug effects; Avoidance Learning - physiology; Cortex (prefrontal); Cyclic AMP - metabolism; Dopamine; Dopamine Agonists - pharmacology; Limbic System - drug effects; Limbic System - metabolism; Male; Opiates; Prefrontal Cortex - drug effects; Prefrontal Cortex - metabolism; Prelimbic cortex; Rats; Rats, Sprague-Dawley; Receptors, Dopamine D1 - agonists; Receptors, Dopamine D1 - metabolism; Reward; Signal Transduction - drug effects; Signal Transduction - physiology
• ISSN: 0028-3908; 1873-7064
• DOI: 10.1016/j.neuropharm.2012.10.029

Dopamine (DA) receptor transmission through either D1 or D2-like subtypes is involved critically in the processing of emotional information within the medial prefrontal cortex (mPFC). However the functional role of specific DA D1-like receptor transmission in the expression of emotionally salient associative memories (either aversive or rewarding) is not currently understood. Here we demonstrate that specific activation of DA D1 receptors in the prelimbic (PLC) division of the mPFC causes a transient block in the behavioral expression of both aversive and rewarding associative memories. We report that intra-PLC microinfusions of a selective D1 receptor agonist block the spontaneous expression of an associative olfactory fear memory, without altering the stability of the original memory trace. Furthermore, using an unbiased place conditioning procedure (CPP), intra-PLC D1 receptor activation blocks the spontaneous expression of an associative morphine (5 mg/kg; i.p.) reward memory, while leaving morphine-primed memory expression intact. Interestingly, both intra-PLC D1-receptor mediated block of either fear-related or reward-related associative memories were dependent upon downstream cyclic-AMP (cAMP) signaling as both effects were rescued by co-administration of a cAMP signaling inhibitor. The blockade of both rewarding and aversive associative memories is mediated through a D1-specific signaling pathway, as neither forms of spontaneous memory expression were blocked by intra-PLC microinfusions of a D2-like receptor agonist. Our results demonstrate that the spontaneous expression of either rewarding or aversive emotionally salient memories shares a common, D1-receptor mediated substrate within the mPFC. ► D1 receptor activation in prelimbic cortex blocks aversive or reward memory recall. ► The original memory traces are left intact. ► Blockade of memory recall is mediated through a cyclic AMP dependent mechanism. ► D2-like receptor stimulation has no effect on memory recall.