Abstract | BACKGROUND: METHODS: The effects of E coli infusion and of infusion of anti-TNF antibodies and a xanthine derivative ( HWA 138) on complement activation and cytokine release was evaluated in 17 baboons. All animals received 5 x 10(8) live bacteria per kg body weight. Five animals received only bacteria, five received in addition 0.5 mg per kg body weight of anti-TNF-antibody, and seven received an infusion of 6 mg per kg body weight of HWA 138 in addition to the bacteria. RESULTS: In baboons receiving 5 x 10(8) live E coli per kg body weight increased plasma levels of TCC, TNF-alpha and IL-8 were found. The release of TNF-alpha was lower in the group receiving HWA 138 at 2 h after the infusion. In baboons receiving an infusion of anti-TNF antibody the concentration of IL-8 was lower at 2 and 4 h than in animals receiving just E coli or HWA 138. CONCLUSION: Infusion of anti-TNF-antibody before E coli infusion will decrease the formation of IL-8. Infusion of HWA 138 before the E coli infusion will also inhibit the formation of TNF-alpha.
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Authors | A Bengtsson, H Redl, G Schlag, T E Mollnes, K Högåsen |
Journal | Acta anaesthesiologica Scandinavica
(Acta Anaesthesiol Scand)
Vol. 40
Issue 2
Pg. 244-9
(Feb 1996)
ISSN: 0001-5172 [Print] England |
PMID | 8848926
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies
- Complement Membrane Attack Complex
- Interleukin-8
- Tumor Necrosis Factor-alpha
- Xanthines
- 1-(5-hydroxy-5-methylhexyl)-3-methylxanthine
- Pentoxifylline
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Topics |
- Animals
- Antibodies
(administration & dosage)
- Complement Activation
- Complement Membrane Attack Complex
(metabolism)
- Escherichia coli Infections
(immunology, physiopathology)
- Hemodynamics
- Interleukin-8
(biosynthesis)
- Male
- Papio
- Pentoxifylline
(analogs & derivatives, pharmacology)
- Sepsis
(immunology, physiopathology)
- Tumor Necrosis Factor-alpha
(biosynthesis, immunology)
- Xanthines
(pharmacology)
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