Exploring the effects of adolescent social isolation stress on the serotonin system and ethanol-motivated behaviors.

Rationale: Alcohol is one of the most frequently used drugs of abuse and has a major impact on human health worldwide. People assigned female at birth and those with adverse childhood experiences are stress-vulnerable and more likely to report drinking as a means of "self-medication." Prior studies...

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Publicado en:Psychopharmacology Vol. 242; no. 4; pp. 763 - 782
Autores principales: McElroy, Bryan D., Li, Chen, McCloskey, Nicholas S., Alberici, Amber R., Kirby, Lynn G.
Formato: Journal Article
Publicado: Springer Nature Apr2025
Acceso en línea:Ver este registro en EBSCOhost
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      pub: Springer Nature
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        10.1007/s00213-025-06749-3
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        atl: Exploring the effects of adolescent social isolation stress on the serotonin system and ethanol-motivated behaviors.
      aug:
        au:
          McElroy, Bryan D.
          Li, Chen
          McCloskey, Nicholas S.
          Alberici, Amber R.
          Kirby, Lynn G.
        affil: https://ror.org/00kx1jb78 Center for Substance Abuse Research, Lewis Katz School of Medicine at Temple University, 3500 N. Broad St, MERB Room 857, 19140, Philadelphia, PA, USA
      sug:
      ab: Rationale: Alcohol is one of the most frequently used drugs of abuse and has a major impact on human health worldwide. People assigned female at birth and those with adverse childhood experiences are stress-vulnerable and more likely to report drinking as a means of "self-medication." Prior studies in our laboratory showed that adolescent social isolation stress (SIS) increases vulnerability to ethanol (EtOH) intake and consumption despite negative consequences in female rats. Objectives: Here, we explored modulation of the dorsal raphe nucleus (DRN)-serotonin (5-HT) system, a sexually dimorphic neurotransmitter system involved in stress-reward interactions, to determine its contribution to EtOH-motivated behaviors in rats that have undergone SIS. Results: We employed electrophysiological and functional neuroanatomy strategies to show that both SIS and EtOH exposure induce persistent hypofunction of the DRN 5-HT system, particularly in females. Chemogenetic activation of DRN 5-HT neurons attenuated reward value for both EtOH and sucrose and elevated punished responding for EtOH in a stress-dependent manner. Conclusions: Our results highlight an inverse relationship between EtOH consumption and the 5-HT system, the sex- and stress-dependent nature of this relationship, and a connection between DRN 5-HT signaling and acute responding to rewards and punishment. These data support the DRN 5-HT system as a potential target to treat aberrant alcohol consumption and drinking despite negative consequences in stress-vulnerable populations.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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