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1 Centre de Recherche en
Nutrition Humaine et Institut National de la Recherche Agronomique,
To explore the regulation of the acute
phase response in vivo, the effects of pentoxifylline (PX) treatment
(100 mg/kg ip 1 h before infection) were investigated in infected and
pair-fed rats 2 and 6 days after an intravenous injection of live
bacteria (Escherichia coli). PX
treatment prevented the increase in plasma tumor necrosis factor
(TNF)-
(peak 1.5 h after the infection) and resulted in
an 84 and 61% inhibition of plasma interleukin (IL)-1
and IL-6,
respectively (peaks at 3 h). Plasma corticosterone kinetics were not
modified by the treatment. Infection increased
1-acid glycoprotein (AGP),
2-macroglobulin (A2M), and
fibrinogen plasma concentrations and decreased albumin levels. PX
significantly reduced AGP plasma concentration as early as
day 2 in infected animals but reduced
A2M and fibrinogen plasma levels only at day 6. The treatment had no effect on the albumin plasma
concentration. Hepatic AGP and fibrinogen mRNA levels increased in
infected rats, whereas those of A2M were unchanged and those of albumin
were decreased. Two days after infection, AGP and fibrinogen mRNA
levels were reduced in treated infected animals. PX was ineffective in modifying those of A2M and albumin. These data demonstrate, in vivo,
that different acute phase proteins are individually regulated in
sepsis. The in vivo effects of PX treatment support the hypothesis that
TNF-
plays an important role in the regulation of AGP production, whereas other factors seem to be involved in the regulation of A2M,
fibrinogen, and albumin expression.
tumor necrosis factor; interleukin-1; interleukin-6
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