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J Neurosci. 2017 Nov 8;37(45):10867-10876. doi: 10.1523/JNEUROSCI.1821-17.2017.

Circuit and Synaptic Plasticity Mechanisms of Drug Relapse.

Author information

1
Department of Neuroscience, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, yandong@pitt.edu yavin.shaham@nih.gov.
2
Department of Psychiatry, Yale School of Medicine, Yale University, New Haven, Connecticut 06511.
3
Department of Neuroscience, Chicago Medical School, Rosalind Franklin University of Medicine and Science, Chicago, Illinois 60064, and.
4
Behavioral Neuroscience Branch, Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Bethesda, Maryland 20892 yandong@pitt.edu yavin.shaham@nih.gov.

Abstract

High rates of relapse to drug use during abstinence is a defining feature of human drug addiction. This clinical scenario has been studied at the preclinical level using different animal models in which relapse to drug seeking is assessed after cessation of operant drug self-administration in rodents and monkeys. In our Society for Neuroscience (SFN) session entitled "Circuit and Synaptic Plasticity Mechanisms of Drug Relapse," we will discuss new developments of our understanding of circuits and synaptic plasticity mechanisms of drug relapse from studies combining established and novel animal models with state-of-the-art cellular, electrophysiology, anatomical, chemogenetic, and optogenetic methods. We will also discuss the translational implications of these new developments. In the mini-review that introduces our SFN session, we summarize results from our laboratories on behavioral, cellular, and circuit mechanisms of drug relapse within the context of our session.

KEYWORDS:

CP-AMPARs; Daun02 inactivation; alcohol; circuit ablation; cocaine; diphtheria toxin receptors; drug cues; homeostatic plasticity; incubation of drug craving; reinstatement; relapse; silent synapse

PMID:
29118216
PMCID:
PMC5678019
DOI:
10.1523/JNEUROSCI.1821-17.2017
[Indexed for MEDLINE]
Free PMC Article

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