Pharmacological inhibition of glycogen synthase kinase 3 increases operant alcohol self-administration in a manner associated with altered pGSK-3β, protein interacting with C kinase and GluA2 protein expression in the reward pathway of male C57BL/6J mice.

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Bibliographic Details
Title: Pharmacological inhibition of glycogen synthase kinase 3 increases operant alcohol self-administration in a manner associated with altered pGSK-3β, protein interacting with C kinase and GluA2 protein expression in the reward pathway of male C57BL/6J mice.
Authors: Faccidomo S; Bowles Center for Alcohol Studies., Holstein SE; Bowles Center for Alcohol Studies., Santanam TS; Bowles Center for Alcohol Studies., Saunders BL; Bowles Center for Alcohol Studies., Swaim KS; Bowles Center for Alcohol Studies., Reid GT; Bowles Center for Alcohol Studies., O'Neill C; Bowles Center for Alcohol Studies., Eastman VR; Bowles Center for Alcohol Studies., Hodge CW; Bowles Center for Alcohol Studies.; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Source: Behavioural pharmacology [Behav Pharmacol] 2020 Feb; Vol. 31 (1), pp. 15-26.
Publication Type: Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: Lippincott Williams and Wilkins Country of Publication: England NLM ID: 9013016 Publication Model: Print Cited Medium: Internet ISSN: 1473-5849 (Electronic) Linking ISSN: 09558810 NLM ISO Abbreviation: Behav Pharmacol Subsets: MEDLINE
Database: MEDLINE Ultimate
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