Gene expression and cytokine and enzyme activation in the liver after a burn injury

J Burn Care Rehabil. 2000 Mar-Apr;21(2):135-41. doi: 10.1097/00004630-200021020-00009.

Abstract

The liver plays a critical role in the inflammatory response to injury; however, the mechanisms by which the liver is affected and how it influences the rest of the immune system are not well understood. Partial hepatectomy is a direct injury to the liver, whereas a burn is an indirect injury to liver, but both injuries appear to produce damage to the liver. In this study, we used a mouse model of 25% total body surface area and 40% total body surface area full-thickness burns to investigate the mechanism of liver damage and response to burn injury by measuring levels of c-Jun messenger (m)RNA, NFkappaB nuclear protein, interleukin-6, transaminases, and liver tissue histology over time. c-Jun and NFkappaB are 2 transcription factors that are induced by partial hepatectomy and related to hepatocyte injury and growth. In both groups of mice with burns, expression of c-Jun mRNA and NFkappaB nuclear protein was activated within 30 minutes after the burn injury, followed by increased levels of interleukin-6 and, finally, elevated enzyme levels. Liver injuries were similar in both groups despite the magnitude of the burns. We believe that these gene products are initiated in the hepatocyte injury after a burn and that they precede other inflammatory responses such as cytokine release, plasma transaminase levels, and histologic changes.

Publication types

  • Comparative Study

MeSH terms

  • Alanine Transaminase / metabolism
  • Ammonia / blood
  • Analysis of Variance
  • Animals
  • Aspartate Aminotransferases / metabolism
  • Burns / genetics*
  • Burns / metabolism*
  • Burns / pathology
  • Culture Techniques
  • Cytokines / analysis
  • Cytokines / metabolism*
  • Disease Models, Animal
  • Gene Expression
  • Genes, jun / genetics*
  • Liver / enzymology*
  • Liver / pathology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • NF-kappa B / metabolism*
  • Necrosis
  • RNA, Messenger / analysis
  • Random Allocation
  • Reference Values

Substances

  • Cytokines
  • NF-kappa B
  • RNA, Messenger
  • Ammonia
  • Aspartate Aminotransferases
  • Alanine Transaminase