| Literature DB >> 31821832 |
Corey B Puryear1, Julie Brooks1, Laura Tan1, Karen Smith1, Yan Li1, Jacobi Cunningham1, Mark S Todtenkopf1, Reginald L Dean1, Connie Sanchez2.
Abstract
Major depressive disorder (MDD) is a heterogeneous clinical syndrome involving distinct pathological processes. Core features of MDD include anhedonia, reduced motivation, increased anxiety, negative affective bias, cognitive impairments, and dysregulated neuroplasticity mechanisms. There are multiple biological hypotheses related to MDD, including dysfunction of the opioid system. Although opium was abandoned as an antidepressant after the introduction of monoaminergic drugs, there has been renewed interest in targeting the opioid system for MDD. In this review, we discuss the preclinical support of this idea using a neurocircuitry- and molecular neuroplasticity-based approach. This article highlights how the opioid system potently modulates mesolimbic circuitry underlying motivation and reward processing, limbic circuitry underlying fear and anxiety responses, cortical and hippocampal circuitry underlying a variety of cognitive functions, as well as broad functional and structural plasticity mechanisms. Ultimately, a more thorough understanding of how the opioid system modulates these core functional domains may lead to novel treatment strategies and molecular targets in the treatment of MDD.Entities:
Keywords: Cognition; Major depressive disorder; Negative valence; Neural circuits; Neuroplasticity; Opioid receptors; Opioid system; Positive valence; Research domain criterion (RDoC)
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Year: 2019 PMID: 31821832 DOI: 10.1016/j.neubiorev.2019.12.007
Source DB: PubMed Journal: Neurosci Biobehav Rev ISSN: 0149-7634 Impact factor: 8.989