Severe burns induce a state of immunosuppression, and the inflammatory resp
onse after burn injury may play a role in this phenomenon. This study exami
ned the effect of the inflammatory response to endotoxin on burn-induced im
munosuppression and oxidative stress, An endotoxin-resistant mouse strain (
C3H/HeJ) and a normally responding mouse strain (C3H/HeN) were compared. Th
e mice were separated into three groups of five animals for each experiment
al day: (1) saline, (2) buprenorphine, and (3) buprenorphine and 20% total
body surface area burn. All animals were fed ad libitum. The inflammatory r
esponse was studied at 1, 4, 7, 10, and 14 days postburn, Proliferation of
activated splenocytes in built mice was significantly lower on days 7, 10,
and 14 for the C3H/HeJ strain and on days 4 and 10 for the C3H/HeN strain.
Globally, C3H/HeJ presented stronger immune suppression than C3H/HeN. Oxida
tive stress parameters (liver malonaldehyde, spleen metabolic activity, and
thiol concentrations) were higher in endotoxin-resistant mice than in the
control strain. Impairment of the inflammatory response was more pronounced
and oxidative stress was greater in endotoxin-resistant burn mice than in
normal burn controls. Buprenorphine administration was not related to depre
ssion of these immune parameters. The inflammatory response following burn
injury may be beneficial to the immune system. (C) 2000 Academic Press.