Possible involvement of p38 MAP kinase in HSP70 expression induced by hypoxia in rat primary astrocytes

Brain Res. 1999 Mar 27;823(1-2):226-30. doi: 10.1016/s0006-8993(99)01178-6.

Abstract

The aim of this study was to elucidate the possible mechanism of HSP induction in response to hypoxia in rat primary astrocytes. Treatment with SB203580, a selective p38 MAP kinase (p38 MAPK) inhibitor, attenuated the increase in HSP70 in a concentration-dependent manner. p38 MAPK was activated in response to hypoxic treatment. These results suggest that p38 MAPK positively regulates hypoxia-induced HSP70 expression in astrocytes.

MeSH terms

  • Animals
  • Astrocytes / metabolism*
  • Brain / cytology
  • Brain / metabolism
  • Calcium-Calmodulin-Dependent Protein Kinases / antagonists & inhibitors
  • Calcium-Calmodulin-Dependent Protein Kinases / physiology*
  • Cells, Cultured
  • Enzyme Inhibitors / pharmacology
  • HSP70 Heat-Shock Proteins / antagonists & inhibitors
  • HSP70 Heat-Shock Proteins / metabolism*
  • Hypoxia / metabolism*
  • Imidazoles / pharmacology
  • Mitogen-Activated Protein Kinases*
  • Pyridines / pharmacology
  • Rats
  • Rats, Wistar
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Enzyme Inhibitors
  • HSP70 Heat-Shock Proteins
  • Imidazoles
  • Pyridines
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • SB 203580