Regulation of alcohol drinking by ventral striatum and extended amygdala circuitry.

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  • Author(s): Borrego MB;Borrego MB;Borrego MB; Chan AE; Chan AE; Chan AE; Ozburn AR; Ozburn AR; Ozburn AR
  • Source:
    Neuropharmacology [Neuropharmacology] 2022 Jul 01; Vol. 212, pp. 109074. Date of Electronic Publication: 2022 Apr 26.
  • Publication Type:
    Journal Article; Review; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • Language:
    English
  • Additional Information
    • Source:
      Publisher: Pergamon Press Country of Publication: England NLM ID: 0236217 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-7064 (Electronic) Linking ISSN: 00283908 NLM ISO Abbreviation: Neuropharmacology Subsets: MEDLINE
    • Publication Information:
      Publication: Oxford : Pergamon Press
      Original Publication: Oxford, New York, Pergamon.
    • Subject Terms:
    • Abstract:
      Alcohol use disorder is a complex psychiatric disorder that can be modeled in rodents using a number of drinking paradigms. Drinking-in-the-dark (DID) is widely used to model the binge/intoxication stage of addiction, and chronic intermittent ethanol vapor procedures (CIE) are used to induce dependence and model withdrawal/negative affect induced escalation of drinking. We discuss experiments showing the ventral striatum (vStr) and extended amygdala (EA) are engaged in response to ethanol in rodents through c-Fos/Fos immunoreactivity studies. We also discuss experiments in rodents that span a wide variety of techniques where the function of vStr and EA structures are changed following DID or CIE, and the role of neurotransmitter and neuropeptide systems studies in these ethanol-related outcomes. We note where signaling systems converge across regions and paradigms and where there are still gaps in the literature. Dynorphin/κ-opioid receptor (KOR) signaling, as well as corticotropin releasing factor (CRF)/CRF receptor signaling were found to be important regulators of drinking behaviors across brain regions and drinking paradigms. Future research will require that females and a variety of rodent strains are used in preclinical experiments in order to strengthen the generalizability of findings and improve the likelihood of success for testing potential therapeutics in human laboratory studies.
      (Published by Elsevier Ltd.)
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    • Grant Information:
      IK2 BX002488 United States BX BLRD VA; T32 AA007468 United States AA NIAAA NIH HHS; U01 AA013519 United States AA NIAAA NIH HHS; I01 BX004699 United States BX BLRD VA; P60 AA010760 United States AA NIAAA NIH HHS
    • Contributed Indexing:
      Keywords: Alcohol; Chronic intermittent ethanol; Drinking-in-the-dark; Extended amygdala; Ventral striatum
    • Accession Number:
      0 (Receptors, Corticotropin-Releasing Hormone)
      3K9958V90M (Ethanol)
      9015-71-8 (Corticotropin-Releasing Hormone)
    • Publication Date:
      Date Created: 20220429 Date Completed: 20220519 Latest Revision: 20221123
    • Publication Date:
      20240105
    • Accession Number:
      PMC9677601
    • Accession Number:
      10.1016/j.neuropharm.2022.109074
    • Accession Number:
      35487273