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Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on September 22, 2006; DOI: 10.1124/jpet.106.110890


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Received for publication July 17, 2006.
Revised September 5, 2006.
Accepted for publication September 21, 2006.

Differential effects of systemic ethanol administration on PKC{epsilon}, {gamma} and {beta} isoform expression, membrane translocation and target phosphorylation: Reversal by chronic ethanol exposure

Sandeep Kumar 1, Brandon M. Lane 1, A. Leslie Morrow 1*

1 University of North Carolina at Chapel Hill

* Address correspondence to: E-mail: morrow{at}med.unc.edu

Abstract

Systemic ethanol administration alters protein kinase C (PKC) activity in brain, but the effects of ethanol on the expression and translocation of specific isoforms are unknown. Rats were administered ethanol (2 g/kg, i.p.) or saline and PKC levels were measured in the cytosolic and membrane fractions by western blot analysis. PKC{epsilon} expression was increased in the cytosol and decreased in the membrane (P2) fraction of cerebral cortex at 10 minutes. At 60 minutes, expression of PKC{epsilon} in the P2 fraction was increased by 42.2±12% but cytosolic levels were unchanged. In contrast, PKC{gamma} in the P2 fraction was decreased 32.7±7% at 60 minutes, but not at 10 minutes, post-ethanol administration. PKC{gamma} levels in the cytosol were reduced at 10 minutes post-ethanol administration and unchanged at 60 minutes. PKC{beta} expression was increased 36±10% and 144±52% in the P2 fraction both at 10 and 60 minutes post-ethanol administration, while cytosolic levels were unchanged. Serine phosphorylation of GABA-A receptor {beta}-chain was reduced and phosphorylation of NMDA receptor NR1 subunit was increased 60 minutes following ethanol administration. There was no effect of acute ethanol administration on PKC isoform levels in the hippocampus. Ethanol challenge did not alter PKC isoform expression in the P2 fraction of cerebral cortex following chronic ethanol administration. These findings suggest that acute ethanol administration alters PKC synthesis and translocation in an isoform and brain region specific manner that leads to alterations in serine phosphorylation of receptors. Furthermore, chronic ethanol administration prevents ethanol-induced alterations in PKC expression in the P2 fraction, where PKC interacts with ethanol-responsive ion channels.


Key words: Ethanol, GABA-A Receptor, Immunoprecipitation, NMDA Receptor, PKC, Phosphorylation


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E. N. Churchill, M.-H. Disatnik, G. R. Budas, and D. Mochly-Rosen
Ethanol for cardiac ischemia: the role of protein kinase c
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[Abstract] [PDF]




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