Literature DB >> 9856954

Regulation of cocaine reward by CREB.

W A Carlezon1, J Thome, V G Olson, S B Lane-Ladd, E S Brodkin, N Hiroi, R S Duman, R L Neve, E J Nestler.   

Abstract

Cocaine regulates the transcription factor CREB (adenosine 3', 5'-monophosphate response element binding protein) in rat nucleus accumbens, a brain region that is important for addiction. Overexpression of CREB in this region decreases the rewarding effects of cocaine and makes low doses of the drug aversive. Conversely, overexpression of a dominant-negative mutant CREB increases the rewarding effects of cocaine. Altered transcription of dynorphin likely contributes to these effects: Its expression is increased by overexpression of CREB and decreased by overexpression of mutant CREB. Moreover, blockade of kappa opioid receptors (on which dynorphin acts) antagonizes the negative effect of CREB on cocaine reward. These results identify an intracellular cascade-culminating in gene expression-through which exposure to cocaine modifies subsequent responsiveness to the drug.

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Year:  1998        PMID: 9856954     DOI: 10.1126/science.282.5397.2272

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  292 in total

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7.  Effects of A-CREB, a dominant negative inhibitor of CREB, on the expression of c-fos and other immediate early genes in the rat SON during hyperosmotic stimulation in vivo.

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9.  Overexpression of the Histone Dimethyltransferase G9a in Nucleus Accumbens Shell Increases Cocaine Self-Administration, Stress-Induced Reinstatement, and Anxiety.

Authors:  Ethan M Anderson; Erin B Larson; Daniel Guzman; Anne Marie Wissman; Rachael L Neve; Eric J Nestler; David W Self
Journal:  J Neurosci       Date:  2017-12-07       Impact factor: 6.167

10.  The glycosyltransferase involved in thurandacin biosynthesis catalyzes both O- and S-glycosylation.

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