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.
Copyright 1999 Elsevier Science B.V.
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