Contrasting Effects of Adolescent and Early-Adult Ethanol Exposure on Prelimbic Cortical Pyramidal Neurons

dc.contributor.authorGalaj, Ewa
dc.contributor.authorGuo, Changyong
dc.contributor.authorHuang, Donald
dc.contributor.authorRanaldi, Robert
dc.contributor.authorMa, Yao-Ying
dc.contributor.departmentPharmacology and Toxicology, School of Medicineen_US
dc.date.accessioned2023-03-30T09:54:47Z
dc.date.available2023-03-30T09:54:47Z
dc.date.issued2020
dc.description.abstractBackground: Adolescence and early-adulthood are vulnerable developmental periods during which binge drinking can have long-lasting effects on brain function. However, little is known about the effects of binge drinking on the pyramidal cells of the prelimbic cortex (PrL) during early and protracted withdrawal periods. Methods: In the present study, we performed whole-cell patch clamp recordings and dendritic spine staining to examine the intrinsic excitability, spontaneous excitatory post-synaptic currents (sEPSCs), and spine morphology of pyramidal cells in the PrL from rats exposed to chronic intermittent ethanol (CIE) during adolescence or early-adulthood. Results: Compared to chronic intermittent water (CIW)-treated controls, the excitability of PrL-L5 pyramidal neurons was significantly increased 21 days after adolescent CIE but decreased 21 days after early-adult CIE. No changes of excitability in PrL Layer (L) 5 were detected 2 days after either adolescent or early-adulthood CIE. Interestingly, decreases in sEPSC amplitude and increases in thin spines ratio were detected 2 days after adolescent CIE. Furthermore, decreased frequency and amplitude of sEPSCs, accompanied by a decrease in the density of total spines and non-thin spines were observed 21 days after adolescent CIE. In contrast, increased frequency and amplitude of sEPSCs, accompanied by increased densities of total spines and non-thin spines were found 21 days after early adult CIE. Conclusion: CIE produced prolonged neuronal and synaptic alterations in PrL-L5, and the developmental stage, i.e., adolescence vs. early-adulthood when subjects receive CIE, is a key factor in determining the direction of these changes.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationGalaj E, Guo C, Huang D, Ranaldi R, Ma YY. Contrasting effects of adolescent and early-adult ethanol exposure on prelimbic cortical pyramidal neurons. Drug Alcohol Depend. 2020;216:108309. doi:10.1016/j.drugalcdep.2020.108309en_US
dc.identifier.urihttps://hdl.handle.net/1805/32120
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.drugalcdep.2020.108309en_US
dc.relation.journalDrug and Alcohol Dependenceen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectAdolescenceen_US
dc.subjectEarly-adulthooden_US
dc.subjectChronic intermittent ethanolen_US
dc.subjectDendritic spineen_US
dc.subjectIntrinsic excitabilityen_US
dc.subjectExcitatory post-synaptic currenten_US
dc.subjectPrelimbic cortexen_US
dc.titleContrasting Effects of Adolescent and Early-Adult Ethanol Exposure on Prelimbic Cortical Pyramidal Neuronsen_US
dc.typeArticleen_US
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