Ethanol reduces p38 kinase activation and cyclin D1 protein expression after partial hepatectomy in rats

J Hepatol. 2006 Feb;44(2):375-82. doi: 10.1016/j.jhep.2005.07.031. Epub 2005 Aug 26.

Abstract

Background/aims: Chronic ethanol consumption inhibits liver regeneration. We examined the effects of chronic ethanol consumption on two mitogen-activated protein kinases in relation to induction of cell cycle proteins after partial hepatectomy (PH).

Methods: Male Wistar rats were ethanol-fed (EF) or pair-fed (PF) for 16 weeks before PH. Hepatic activation of extracellular signal regulated kinase (ERK)1/2, p38 kinase and expression of cyclinD1, cyclin-dependent kinase-4 (cdk4) and proliferating cell nuclear antigen (PCNA) were studied.

Results: In PF rats, PH-induced p38 activation was evident at 2h and was maximal at 12h. There was a close temporal relationship between p38 activation, cyclin D1 and PCNA expression. Alcohol exposure reduced p38 activation, cyclin D1 and PCNA, each by approximately 50%. ERK1/2 activation occurred during the first 2h post-PH in both EF and PF rats, and there was no later increase in PF rats. In vivo inhibition of p38 suppressed PCNA expression whereas the effect of ERK1/2 inhibition was inconsistent.

Conclusions: p38 kinase activation is linked temporally with cyclin D1 expression after PH and appears to exert cell cycle control in the adult liver. p38 signaling also appears to be a target for the inhibitory effect of chronic alcohol on liver regeneration.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcoholism / enzymology*
  • Alcoholism / pathology
  • Animals
  • Blotting, Western
  • Cyclin D1 / biosynthesis
  • Cyclin D1 / genetics*
  • Cyclin-Dependent Kinase 4 / metabolism
  • Disease Models, Animal
  • Enzyme Activation / drug effects
  • Ethanol / toxicity*
  • Gene Expression
  • Hepatectomy*
  • Liver / drug effects
  • Liver / enzymology*
  • Liver / pathology
  • Liver Regeneration / drug effects
  • Male
  • Proliferating Cell Nuclear Antigen / metabolism
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics*
  • Rats
  • Rats, Wistar
  • Reverse Transcriptase Polymerase Chain Reaction
  • p38 Mitogen-Activated Protein Kinases / metabolism*

Substances

  • Proliferating Cell Nuclear Antigen
  • RNA, Messenger
  • Cyclin D1
  • Ethanol
  • Cyclin-Dependent Kinase 4
  • p38 Mitogen-Activated Protein Kinases