| Literature DB >> 26806779 |
Abstract
Opiate addiction, similarly to addiction to other psychoactive drugs, is chronic relapsing brain disease caused by drug-induced short-term and long-term neuroadaptations at the molecular, cellular, and behavioral levels. Preclinical research in laboratory animals has found important interactions between opiate exposure and stress-responsive systems. In this review, we will discuss the dysregulation of several stress-responsive systems in opiate addiction: vasopressin and its receptor system, endogenous opioid systems (including proopiomelanocortin/mu opioid receptor and dynorphin/kappa opioid receptor), orexin and its receptor system, and the hypothalamic-pituitary-adrenal axis. A more complete understanding of how opiates alter these stress systems, through further laboratory-based studies, is required to identify novel and effective pharmacological targets for the long-term treatment of heroin addiction.Entities:
Keywords: Dynorphin; HPA axis; Heroin addiction; Opioid receptor; Orexin; POMC; Stress; V1b receptor; Vasopressin
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Year: 2015 PMID: 26806779 DOI: 10.1016/bs.pbr.2015.09.001
Source DB: PubMed Journal: Prog Brain Res ISSN: 0079-6123 Impact factor: 2.453