期刊
NEUROSCIENCE LETTERS
卷 349, 期 3, 页码 143-146出版社
ELSEVIER IRELAND LTD
DOI: 10.1016/S0304-3940(03)00852-8
关键词
cocaine; glycogen synthase kinase-3 beta; D-1 dopamine receptor; protein kinase; phosphorylation
资金
- NIDA NIH HHS [DA 11029] Funding Source: Medline
Prenatal cocaine exposure in rabbits induces cerebrocortical structural abnormalities. Glycogen synthase kinase-3beta (GSK3beta) plays an important role in neuronal development and survival. This study was designed to examine the effect of prenatal cocaine on brain GSK3beta. Rabbits exposed in utero to cocaine and assessed on postnatal day 20 had increased basal levels of phospho-GSK3beta (ser-9) in frontal cortex (FCX) and striatum, but not hippocampus (HP). However, no changes in GSK3beta expression were detected in the brain regions of treated rabbits. Consistent with the change in GSK3beta activity, levels of beta-catenin, a downstream substrate of GSK3beta, increased in FCX but not in HP of cocaine offspring. Administration of a D, dopamine receptor agonist inhibited GSK3beta activity in FCX and HP of control rabbits but not in cocaine offspring. This loss of GSK3beta inhibition is in accord with the previously demonstrated dysfunction of this receptor in in utero cocaine-exposed animals. The results indicate that prenatal cocaine exposure alters GSK3beta pathway in select brain areas and may underlie the structural changes noted in these animals. (C) 2003 Published by Elsevier Ireland Ltd.
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