Korean J Physiol Pharmacol.  2002 Dec;6(6):319-325.

Blockade of p38 Mitogen-activated Protein Kinase Pathway Inhibits Interleukin-6 Release and Expression in Primary Neonatal Cardiomyocytes

Affiliations
  • 1Department of Pharmacology and Institute of Cardiovascular Research, Chonbuk National University Medical School, Jeonju, Korea. soowan@moak.chonbuk. ac.kr

Abstract

The induction of interleukin-6 (IL-6) using combined proinflammatory agents (LPS/IFN-gamma or TNF-alpha/IFN-gamma) was studied in relation to p38 mitogen-activated protein kinase (MAPK) and NF-kappaB transcriptional factor in primary neonatal cardiomyocytes. When added to cultures of cardiomyocytes, the combined agents (LPS/IFN-gamma or TNF-alpha/IFN-gamma) had stimulatory effect on the production of IL-6 and the elevation was significantly reduced by SB203580, a specific p38 MAPK inhibitor. SB203580 inhibited protein production and gene expression of IL-6 in a concentration-dependent manner. In this study, IFN-gamma enhancement of TNF-alpha-induced NF-kappaB binding affinity as well as p38 MAP kinase activation was observed. However, a specific inhibitor of p38 MAPK, SB203580, had no effect on TNF-alpha/IFN-gamma or LPS/IFN-gamma-induced NF-kappaB activation. This study strongly suggests that these pathways about TNF-alpha/IFN-gamma or LPS/IFN-gamma-activated IL-6 release can be primarily dissociated in primary neonatal cardiomyocytes.

Keyword

Interleukin-6; p38 MAPK; NF-kappaB; SB203580

MeSH Terms

Gene Expression
Interleukin-6*
Myocytes, Cardiac*
NF-kappa B
p38 Mitogen-Activated Protein Kinases
Protein Kinases*
Interleukin-6
NF-kappa B
Protein Kinases
p38 Mitogen-Activated Protein Kinases
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