Alcohol
Volume 31, Issue 1 , Pages 39-48, August 2003

Role of protein kinase C in estrogen protection against apoptotic cerebellar cell death in ethanol-withdrawn rats

  • Marianna E. Jung

      Affiliations

    • Department of Pharmacology and Neuroscience, University of North Texas HSC at Fort Worth, 3500 Camp Bowie Boulevard, Fort Worth, TX 76107-2699, USA
    • Corresponding Author InformationCorresponding author. Tel.: +1-817-735-0156; fax: +1-817-735-2091.
    • ,
  • David G. Watson

      Affiliations

    • Department of The Air Force, 59th Clinical Research Squadron, Lackland Air Force Base, TX 78236, USA
    • ,
  • Yi Wen

      Affiliations

    • Department of Pharmacology and Neuroscience, University of North Texas HSC at Fort Worth, 3500 Camp Bowie Boulevard, Fort Worth, TX 76107-2699, USA
    • ,
  • James W. Simpkins

      Affiliations

    • Department of Pharmacology and Neuroscience, University of North Texas HSC at Fort Worth, 3500 Camp Bowie Boulevard, Fort Worth, TX 76107-2699, USA

Received 19 February 2003; received in revised form 16 June 2003; accepted 6 July 2003.

Editor: T.R. Jerrells

Abstract 

Results of studies from our laboratory have shown that administration of 17β-estradiol (E2) reduces cerebellar neuronal damage during ethanol withdrawal (EW). In the current study, we examined mechanisms underlying E2 protection against EW-associated cerebellar damage by assessing apoptotic indicators: DNA fragmentation, caspase-3 activity, and protein kinase C (PKC) activity. Ovariectomized rats, implanted with E2 or oil pellets, received ethanol [7.5% weight/volume (wt./vol.)] (EW/E2 group and EW/Oil group, respectively) chronically (for 5 weeks) or control dextrin diet (Dextrin/Oil group). At day 14 of EW, cerebelli were collected for the terminal deoxynucleotidyltransferase (TdT)-mediated dUDP-biotin nick end labeling (TUNEL) assay to detect DNA fragmentation and for immunohistochemistry to detect caspase-3 activation. A separate group of rat cerebelli was prepared to assess for total PKC activity, as well as for activity of a specific PKC isozyme, epsilon (PKCε), by using an in vitro [γ-32P]ATP phosphorylation assay at days 1 and 14 of EW. Results indicated that rats in the EW/Oil group had more DNA fragments and caspase-3–positive neuronal cells than observed for control rats, and these effects were inhibited by E2 treatment. For total PKC activity at day 1 of EW, rats in the EW/E2 group had a lower cytosolic PKC activity than observed for either rats in the EW/Oil group or control rats. At day 14 of EW, both EW groups had a lower total PKC activity than observed for control rats. For PKCε activity, rats in the EW/E2 group had a lower cytosolic PKCε activity than observed for rats in the EW/Oil group or for control rats at day 1, and they had a lower membrane PKCε activity at day 14 of EW than observed for control rats. These findings support the suggestion that E2 protects against cerebellar neuronal damage in ethanol-withdrawn rats by inhibition of DNA fragmentation and caspase-3 activation, and that reduced PKC activity may be involved in the protection.

Keywords: Ethanol withdrawal, 17β-estradiol, Apoptosis, PKCε, Rats

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PII: S0741-8329(03)00186-1

doi:10.1016/j.alcohol.2003.07.004

Alcohol
Volume 31, Issue 1 , Pages 39-48, August 2003

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