The Heat Shock Response Inhibits Inducible Nitric Oxide Synthase Gene Expression by Blocking Iκ-B Degradation and NF-κB Nuclear Translocation

1997 ◽  
Vol 231 (2) ◽  
pp. 257-263 ◽  
Author(s):  
Hector R. Wong ◽  
Marnie Ryan ◽  
Jonathan R. Wispé
Keyword(s):  
Gene Expression ◽  
Nitric Oxide ◽  
Heat Shock ◽  
Nitric Oxide Synthase ◽  
Inducible Nitric Oxide Synthase ◽  
Heat Shock Response ◽  
Nuclear Translocation ◽  
Shock Response ◽  
Oxide Synthase ◽  
Inducible Nitric Oxide

Heat shock response inhibits cytokine-inducible nitric oxide synthase expression in rat hepatocytes

Hepatology ◽  
1996 ◽  
Vol 24 (5) ◽  
pp. 1238-1245 ◽  
Author(s):  
M E de Vera ◽  
Y M Kim ◽  
H R Wong ◽  
Q Wang ◽  
T R Billiar ◽  
...  
Keyword(s):  
Nitric Oxide ◽  
Heat Shock ◽  
Nitric Oxide Synthase ◽  
Inducible Nitric Oxide Synthase ◽  
Heat Shock Response ◽  
Rat Hepatocytes ◽  
Shock Response ◽  
Oxide Synthase ◽  
Inducible Nitric Oxide

The Heat Shock Response Inhibits NF-κB Activation, Nitric Oxide Synthase Type 2 Expression, and Macrophage/Microglial Activation in Brain

2000 ◽  
Vol 20 (5) ◽  
pp. 800-811 ◽  
Author(s):  
Michael T. Heneka ◽  
Anthony Sharp ◽  
Thomas Klockgether ◽  
Vitality Gavrilyuk ◽  
Douglas L. Feinstein
Keyword(s):  
Gene Expression ◽  
Nitric Oxide ◽  
Heat Shock ◽  
Nitric Oxide Synthase ◽  
Heat Shock Response ◽  
Inflammatory Gene Expression ◽  
Inflammatory Gene ◽  
Shock Response ◽  
Oxide Synthase

The heat shock response (HSR) provides protection against stress-induced damage, and also prevents initiation of inflammatory gene expression via inhibition of NFκB activation. This article describes experiments demonstrating that the HSR prevents induction of nitric oxide synthase type 2 (NOS2) in rat brain. Twenty four hours after intrastriatal injection of lipopolysaccharide (LPS), IL-1β, and IFN-γ, NOS2 immunoreactive cells were detected in striatum, corpus callosum, and to a lesser extent in cortex. Induction of a HSR by whole body warming to 41°C for 20 minutes, done 1 day before LPS plus cytokine injection, reduced the number of NOS2-positive staining cells to background levels. Staining for ED1 antigen revealed that the HSR also suppressed microglial/brain macrophage activation in the same areas. Striatal injection of LPS and cytokines induced the rapid activation of NFκB, and this activation was prevented by prior HS, which also increased brain IκB-α expression. These results suggest that establishment of a HSR can reduce inflammatory gene expression in brain, mediated by inhibition of NFκB activation, and may therefore offer a novel approach to treatment and prevention of neurological disease and trauma.

Sign in / Sign up

Export Citation Format

Share Document