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Regulation of Na+,K+-ATpase by chronic ethanol exposure of PC 12 cells

  • SUNY Buffalo

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

The effects of chronic ethanol exposure on Na+,K+-ATPase were investigated in PC 12 cells. Inclusion of ethanol in the Na+,K+-ATPase assay (i.e. in vitro addition of ethanol) inhibited enzyme activity. Conversely, intrinsic Na+,K+-ATPase activity was increased after chronic ethanol exposure of the cells. This increase in Na+,K+ pumps occurred without any alteration in the inhibitory effects of in vitro ethanol. A similar response was observed when the chronic treatments were carried out using serum-free defined medium. The effects of other agents, which like ethanol decrease membrane order, were investigated. The addition of ketamine and tert-butanol in vitro caused a concentration-dependent inhibition of Na+,K+-ATPase activity. However, chronic exposure of the PC 12 cells to tert-butanol or ketamine did not alter either intrinsic Na+,K+-ATPase activity or the inhibitory effects of ethanol in vitro. Maintenance of PC 12 cells in medium containing ethanol resulted in an increase in the intracellular content of Na+ without any change in the K+ levels. In contrast, maintenance of the cells in medium containing tert-butanol did not alter intracellular levels of Na+ or K+. The present study shows that the ethanol-induced increase in Na+,K+ pumps involved an increase in the intracellular content of Na+. This increase in Na+ content did not appear to be secondary to an inhibition of Na+,K+-ATPase activity.

Original languageEnglish
Pages (from-to)1653-1658
Number of pages6
JournalBiochemical Pharmacology
Volume45
Issue number8
DOIs
StatePublished - Apr 22 1993

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