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MODERATE ALCOHOL CONSUMPTION INDUCES LASTING IMPACTS ON PREFRONTAL CORTICAL SIGNALING IN MICE.
Smith, Grace C; Griffith, Keith R; Sicher, Avery R; Brockway, Dakota F; Proctor, Elizabeth A; Crowley, Nicole A.
Afiliación
  • Smith GC; Department of Biology, The Pennsylvania State University, University Park, PA, USA 16802.
  • Griffith KR; Department of Biomedical Engineering, The Pennsylvania State University, University Park, PA, USA 16802.
  • Sicher AR; Department of Biology, The Pennsylvania State University, University Park, PA, USA 16802.
  • Brockway DF; Department of Biology, The Pennsylvania State University, University Park, PA, USA 16802.
  • Proctor EA; Neuroscience Graduate Program, Huck Institute of the Life Sciences, The Pennsylvania State University, University Park, PA, USA 16802.
  • Crowley NA; Department of Biology, The Pennsylvania State University, University Park, PA, USA 16802.
bioRxiv ; 2024 Apr 05.
Article en En | MEDLINE | ID: mdl-38617243
ABSTRACT
Both alcohol use disorder (AUD) and Alzheimer's Disease and Related Dementias (ADRD) appear to include disruption in the balance of excitation and inhibition in the cortex, but their potential interactions are unclear. We examined the effect of moderate voluntary binge alcohol consumption on the aged, pre-disease neuronal environment by measuring intrinsic excitability and spontaneous neurotransmission on prefrontal cortical pyramidal (excitatory, glutamatergic) and non-pyramidal (inhibitory, GABAergic) neurons following a prolonged period of abstinence from alcohol in mice. Results highlight that binge alcohol consumption has lasting impacts on the electrophysiological properties of prefrontal cortical neurons. A profound increase in excitatory events onto layer 2/3 non-pyramidal neurons following alcohol consumption was seen, along with altered intrinsic excitability of pyramidal neurons, which could have a range of effects on Alzheimer's Disease progression in humans. These results indicate that moderate voluntary alcohol influences the pre-disease environment in aging and highlight the need for further mechanistic investigation into this risk factor.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article