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Stress vulnerability promotes an alcohol-prone phenotype in a preclinical model of sustained depression.

Authors
  • Riga, Danai1
  • Schmitz, Leanne J M1
  • van Mourik, Yvar2
  • Hoogendijk, Witte J G3
  • De Vries, Taco J1, 2
  • Smit, August B1
  • Spijker, Sabine1
  • 1 Department of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, Vrije Universiteit, Amsterdam, The Netherlands. , (Netherlands)
  • 2 Department of Anatomy and Neurosciences, Amsterdam Neuroscience, Vrije Universiteit Medical Center, Amsterdam, The Netherlands. , (Netherlands)
  • 3 Department of Psychiatry, Erasmus University Medical Center, Rotterdam, The Netherlands. , (Netherlands)
Type
Published Article
Journal
Addiction Biology
Publisher
Wiley (Blackwell Publishing)
Publication Date
Jan 01, 2020
Volume
25
Issue
1
Identifiers
DOI: 10.1111/adb.12701
PMID: 30561063
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

Major depression and alcohol-related disorders frequently co-occur. Depression severity weighs on the magnitude and persistence of comorbid alcohol use disorder (AUD), with severe implications for disease prognosis. Here, we investigated whether depression vulnerability drives propensity to AUD at the preclinical level. We used the social defeat-induced persistent stress (SDPS) model of chronic depression in combination with operant alcohol self-administration (SA). Male Wistar rats were subjected to social defeat (five episodes) and prolonged social isolation (~12 weeks) and subsequently classified as SDPS-prone or SDPS-resilient based on their affective and cognitive performance. Using an operant alcohol SA paradigm, acquisition, motivation, extinction, and cue-induced reinstatement of alcohol seeking were examined in the two subpopulations. SDPS-prone animals showed increased alcohol SA, heightened motivation to acquire alcohol, persistent alcohol seeking despite alcohol unavailability, signs of extinction resistance, and increased cue-induced relapse; the latter could be blocked by the α2 adrenoreceptor agonist guanfacine. In SDPS-resilient rats, prior exposure to social defeat increased alcohol SA without affecting any other measures of alcohol seeking and alcohol taking. Our data revealed that depression proneness confers vulnerability to alcohol, emulating patterns of alcohol dependence seen in human addicts, and that depression resilience to a large extent protects from the development of AUD-like phenotypes. Furthermore, our data suggest that stress exposure alone, independently of depressive symptoms, alters alcohol intake in the long-term. © 2018 The Authors. Addiction Biology published by John Wiley & Sons Ltd on behalf of Society for the Study of Addiction.

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