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Neurobiology of learning and memory v.145, 2017년, pp.151 - 164   SCI SCIE SSCI
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Linking muscarinic receptor activation to UPS-mediated object memory destabilization: Implications for long-term memory modification and storage

Stiver, Mikaela L.    (Department of Psychology and Collaborative Neuroscience Program, University of Guelph, Guelph, Ontario, Canada   ); Cloke, Jacob M.    (Department of Psychology and Collaborative Neuroscience Program, University of Guelph, Guelph, Ontario, Canada   ); Nightingale, Natalie    (Department of Psychology and Collaborative Neuroscience Program, University of Guelph, Guelph, Ontario, Canada   ); Rizos, Julian    (Department of Psychology and Collaborative Neuroscience Program, University of Guelph, Guelph, Ontario, Canada   ); Messer Jr., William S.    (Departments of Pharmacology and Experimental Therapeutics and Medicinal and Biological Chemistry, College of Pharmacy and Pharmaceutical Sciences, University of Toledo, Toledo, OH, USA   ); Winters Jr., Boyer D.    (Department of Psychology and Collaborative Neuroscience Program, University of Guelph, Guelph, Ontario, Canada  );
  • 초록  

    Abstract Consolidated memories can become destabilized during reactivation, resulting in a transient state of instability, a process that has been hypothesized to underlie long-term memory updating. Consistent with this notion, relatively remote memories, which are resistant to standard destabilization procedures, are reliably destabilized when novel information (i.e., the opportunity for memory updating) is present during reactivation. We have also shown that cholinergic muscarinic receptor (mAChR) activation can similarly destabilize consolidated object memories. Synaptic protein degradation via the ubiquitin proteasome system (UPS) has previously been linked to destabilization of fear and object-location memories. Given the role of calcium in regulating proteasome activity, we hypothesized that activation of cholinergic receptors, specifically M 1 mAChRs, stimulates the UPS via inositol triphosphate receptor (IP 3 R)-mediated release of intracellular calcium stores to facilitate object memory destabilization. We present converging evidence for this hypothesis, which we tested using a modified spontaneous object recognition task for rats and microinfusions into perirhinal cortex (PRh), a brain region strongly implicated in object memory. We extend our previous findings by demonstrating that M 1 mAChRs are necessary for novelty-induced object memory destabilization. We also show that proteasome inhibition or IP 3 R antagonism in PRh prevents object memory destabilization induced by novelty or M 1 mAChR stimulation. These results establish an intracellular pathway linking M 1 receptors, IP 3 Rs, and UPS activity to object memory destabilization and suggest a previously unacknowledged role for cholinergic signaling in long-term memory modification and storage. Highlights Muscarinic receptor (mAChR) activation promotes object memory destabilization. The ubiquitin proteasome system (UPS) destabilizes synaptic proteins and memories. M 1 mAChR activation underlies the muscarinic effects on object memories. UPS inhibition prevents memory destabilization prompted by M 1 activation. M 1 mAChRs might stimulate the UPS via IP 3 receptor-induced calcium release.


  • 주제어

    Acetylcholine .   Labile .   Prediction error .   Recognition .   Reconsolidation .   Ubiquitin proteasome system.  

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