| Literature DB >> 15470231 |
Daniel S Perrien1, Elizabeth C Wahl, William R Hogue, Ulrich Feige, James Aronson, Martin J J Ronis, Thomas M Badger, Charles K Lumpkin.
Abstract
We tested the hypothesis that combined administration of IL-1 and TNF antagonists would protect fracture healing from inhibition by chronic ethanol exposure. Adult male rats were fed a liquid diet +/- ethanol (CON and ETOH) by intragastric infusion for three weeks prior to and three weeks after creation of an externally fixated tibial fracture. Beginning the day of fracture, one-half of each dietary group received 2.0 mg/kg/day IL-1ra and 2.0 mg/kg/2-days sTNFR1 (CON + ANTAG and ETOH + ANTAG), while all other animals received vehicle alone (CON + VEH and ETOH + VEH). Scoring of ex vivo radiographs and analysis by pQCT revealed a significantly lower incidence of bridging and reduced total mineral content in the ETOH + VEH group compared to all other groups. These results support, for the first time, the hypothesis that IL-1 and TNF antagonists are capable of protecting fracture healing from the inhibition associated with chronic ethanol consumption.Entities:
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Year: 2004 PMID: 15470231 DOI: 10.1093/toxsci/kfi002
Source DB: PubMed Journal: Toxicol Sci ISSN: 1096-0929 Impact factor: 4.849