Mitogen Activated Protein Kinases in Steatotic and Non-Steatotic Livers Submitted to Ischemia-Reperfusion

Int J Mol Sci. 2019 Apr 10;20(7):1785. doi: 10.3390/ijms20071785.

Abstract

: We analyzed the participation of mitogen-activated protein kinases (MAPKs), namely p38, JNK and ERK 1/2 in steatotic and non-steatotic livers undergoing ischemia-reperfusion (I-R), an unresolved problem in clinical practice. Hepatic steatosis is a major risk factor in liver surgery because these types of liver tolerate poorly to I-R injury. Also, a further increase in the prevalence of steatosis in liver surgery is to be expected. The possible therapies based on MAPK regulation aimed at reducing hepatic I-R injury will be discussed. Moreover, we reviewed the relevance of MAPK in ischemic preconditioning (PC) and evaluated whether MAPK regulators could mimic its benefits. Clinical studies indicated that this surgical strategy could be appropriate for liver surgery in both steatotic and non-steatotic livers undergoing I-R. The data presented herein suggest that further investigations are required to elucidate more extensively the mechanisms by which these kinases work in hepatic I-R. Also, further researchers based in the development of drugs that regulate MAPKs selectively are required before such approaches can be translated into clinical liver surgery.

Keywords: ischemic-reperfusion injury; mitogen activated protein kinases; non-alcoholic fatty liver disease; steatosis.

Publication types

  • Review

MeSH terms

  • Animals
  • Fatty Liver* / metabolism
  • Fatty Liver* / pathology
  • Fatty Liver* / physiopathology
  • Fatty Liver* / therapy
  • Humans
  • Ischemic Preconditioning*
  • Liver* / metabolism
  • Liver* / pathology
  • Liver* / physiopathology
  • MAP Kinase Signaling System*
  • Mitogen-Activated Protein Kinases / metabolism*
  • Reperfusion Injury* / metabolism
  • Reperfusion Injury* / pathology
  • Reperfusion Injury* / physiopathology
  • Reperfusion Injury* / prevention & control

Substances

  • Mitogen-Activated Protein Kinases