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Chronic poly-drug administration damages adult mouse brain neural stem cells.
McGrath, Erica L; Schlagal, Caitlin R; Cortez, Ibdanelo; Dunn, Tiffany J; Gao, Junling; Fox, Robert G; Stutz, Sonja J; Kuo, Yong-Fang; Hommel, Jonathan D; Dineley, Kelly T; Cunningham, Kathryn A; Kaphalia, Bhupendra S; Wu, Ping.
Afiliação
  • McGrath EL; Department of Neuroscience, Cell Biology and Anatomy, University of Texas Medical Branch, Galveston, TX 77555, USA; Institute for Translational Sciences, University of Texas Medical Branch, Galveston, TX 77555, USA; Center for Addiction Research, University of Texas Medical Branch, Galveston, TX 775
  • Schlagal CR; Department of Neuroscience, Cell Biology and Anatomy, University of Texas Medical Branch, Galveston, TX 77555, USA; Center for Addiction Research, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Cortez I; Department of Neurology, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Dunn TJ; Department of Neuroscience, Cell Biology and Anatomy, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Gao J; Department of Neuroscience, Cell Biology and Anatomy, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Fox RG; Center for Addiction Research, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Stutz SJ; Center for Addiction Research, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Kuo YF; Department of Preventive Medicine and Community Health, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Hommel JD; Institute for Translational Sciences, University of Texas Medical Branch, Galveston, TX 77555, USA; Center for Addiction Research, University of Texas Medical Branch, Galveston, TX 77555, USA; Department of Pharmacology and Toxicology, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Dineley KT; Center for Addiction Research, University of Texas Medical Branch, Galveston, TX 77555, USA; Department of Neurology, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Cunningham KA; Institute for Translational Sciences, University of Texas Medical Branch, Galveston, TX 77555, USA; Center for Addiction Research, University of Texas Medical Branch, Galveston, TX 77555, USA; Department of Pharmacology and Toxicology, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Kaphalia BS; Department of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Wu P; Department of Neuroscience, Cell Biology and Anatomy, University of Texas Medical Branch, Galveston, TX 77555, USA; Center for Addiction Research, University of Texas Medical Branch, Galveston, TX 77555, USA. Electronic address: piwu@utmb.edu.
Brain Res ; 1723: 146425, 2019 11 15.
Article em En | MEDLINE | ID: mdl-31473223
ABSTRACT
Cocaine and ethanol are two commonly co-abused substances; however, the neuropathology following chronic dual consumption is poorly understood. Neural stem cells (NSCs) are a subpopulation of cells within the adult brain that are integral to brain maintenance and repair making them an appealing target to reverse neurodegeneration associated with abused substances. Yet, knowledge about NSC response to chronic poly-drug administration of ethanol and cocaine is minimal. Here, we developed a novel chronic poly-drug administration paradigm of ethanol and cocaine using a transgenic mouse model to trace endogenous NSC survival and differentiation in three brain regions from both male and female mice. We report significant and distinct patterns of NSC survival and differentiation among brain regions, as well as between sexes. Additionally, poly-drug administration had synergistic effects on NSC survival. Altered cognitive and hedonic behaviors were also observed, however the extent of these behavioral changes was not proportional to the NSC changes. With this mouse model we can effectively examine cognitive and behavioral changes and correlate them with pathological changes in the brain in response to chronic poly-drug administration, which is of great value in understanding the progression of neurodegeneration in polysubstance use disorders and evaluation potential therapeutics on neuroregeneration.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cocaína / Etanol / Células-Tronco Neurais Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cocaína / Etanol / Células-Tronco Neurais Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article