Effect of p38 MAP kinases on contractility and ischemic injury in intact heart

Acta Physiol Hung. 2009 Sep;96(3):307-23. doi: 10.1556/APhysiol.96.2009.3.5.

Abstract

The p38 MAP kinases are stress-activated MAP kinases whose induction is often associated with the onset of heart failure. This study investigated the role of p38 MAP kinase isoforms in the regulation of myocardial contractility and ischemia/reperfusion injury using mice with cardiac-specific expression of kinase dead (dominant negative) mutants of p38alpha (p38alphadn) or p38beta (p38betadn). Hearts were subjected to 20 min ischemia and 40 min reperfusion. Immunofluorescence staining for p38alphadn and p38betadn protein was performed on neonatal cardiomyocytes infected with adenovirus expressing flag-tagged p38alphadn and p38betadn protein. Basal contractile function was increased in both p38alphadn and p38betadn hearts compared to WT. Ischemic injury was increased in p38betadn vs. WT hearts, as indicated by lower posti-schemic recoveries of contractile function and ATP. However, despite a similar increase in contractility, ischemic injury was not increased in p38alphadn vs. WT hearts. Immunohistological analysis of cardiomyocytes with comparable levels of protein overexpression show that p38alphadn and p38betadn proteins were co-localized with sarcomeric alpha-actinin, however, p38alphadn was detected in the nucleus while p38betadn was exclusively detected in the cytosol. In summary, attenuated p38 activity led to increased myocardial contractility; specific isoforms of p38 and their sub-cellular localization may have different roles in modulating ischemic injury.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Animals, Newborn
  • Cell Nucleus / enzymology
  • Cells, Cultured
  • Cytosol / enzymology
  • Disease Models, Animal
  • Humans
  • Hydrogen-Ion Concentration
  • Isoenzymes
  • Mice
  • Mice, Transgenic
  • Mitogen-Activated Protein Kinase 11 / genetics
  • Mitogen-Activated Protein Kinase 11 / metabolism*
  • Mitogen-Activated Protein Kinase 14 / genetics
  • Mitogen-Activated Protein Kinase 14 / metabolism*
  • Mutation
  • Myocardial Contraction*
  • Myocardial Reperfusion Injury / enzymology*
  • Myocardial Reperfusion Injury / physiopathology
  • Myocardium / enzymology*
  • Myosin Heavy Chains / genetics
  • Phosphocreatine / metabolism
  • Promoter Regions, Genetic
  • Rats
  • Rats, Sprague-Dawley
  • Recovery of Function
  • Time Factors
  • Transfection
  • Ventricular Myosins / genetics

Substances

  • Isoenzymes
  • Phosphocreatine
  • Adenosine Triphosphate
  • Mitogen-Activated Protein Kinase 11
  • Mitogen-Activated Protein Kinase 14
  • Ventricular Myosins
  • Myosin Heavy Chains