Deferoxamine reduces tissue injury and lethality in LPS-treated mice

Citation
M. Vulcano et al., Deferoxamine reduces tissue injury and lethality in LPS-treated mice, INT J IMMUN, 22(8), 2000, pp. 635-644
Citations number
49
Categorie Soggetti
Immunology
Journal title
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY
ISSN journal
01920561 → ACNP
Volume
22
Issue
8
Year of publication
2000
Pages
635 - 644
Database
ISI
SICI code
0192-0561(200008)22:8<635:DRTIAL>2.0.ZU;2-7
Abstract
We studied the effect of deferoxamine (DFX), an iron chelator, which can al so act as a free radical scavenger, in an experimental murine model of seps is. In vivo studies demonstrated that: pretreatment of mice with DFX reduce s tumor necrosis factor alpha (TNF-alpha) serum levels and increases the ra te of survival of mice inoculated with lethal doses of lipopolysaccharide ( LPS) or Escherichia coli O111:B4. By using the iron chelated form of DFX (f errioxamine) the same results were obtained, suggesting that in this model, DFX could act as a free radical scavenger. On the other hand, DFX prevents mortality induced either by LPS or murine recombinant TNF-alpha in D(+)-ga lactosamine (Ga1N)-sensitized mice. These protective actions of DFX correla te with an attenuated tissue damage observed in lungs, livers and kidneys o f LPS-treated animals and Ga1N-sensitized mice inoculated with TNF-alpha. ( C) 2000 International Society for Immunopharmacology, Published by Elsevier Science Ltd. All rights reserved.