Effect of ethanol and sodium arsenite on HSP-72 formation and on survival in a murine endotoxin model

George D. Lappas, Irene E. Karl, Richard S. Hotchkiss

Research output: Contribution to journalArticle

35 Scopus citations

Abstract

Recently, investigators reported that prophylactic hyperthermia and induction of heat shock proteins (HSPs) decreased mortality from endotoxin. Although the mechanism by which hyperthermia protects is unknown, two possible etiologies are induction of HSPs and/or production of cytokines, interleukin-1α (IL-1α) or tumor necrosis factor-α (TNF-α). The purpose of this study was to determine if in vivo administration of sodium arsenite (NaAsO2) or ethanol, inducers of HSPs in isolated cells, induced HSP-72 production in lung, liver, kidney, and duodenum (organs known to induce HSP-72 by heat) and improved survival from endotoxin. Female ND4 mice were injected intraperitoneally with either NaAsO2 (5.25 mg/kg body weight) or ethanol (4.0 g/kg), immediately, 8 or 18 h prior to Escherichia coil endotoxin injection (20 mg/kg). Both compounds improved short-term (24 h) survival twofold (p < .01), but failed to improve long-term (7 days) survival. Simultaneous injection of ethanol with endotoxin improved both short-term survival twofold (p < .01), and long-term survival 5-fold (p < .001). Ethanol induced HSP-72 in kidney, 50% that of the standard (i.e., pooled livers isolated from heat-treated mice); NaAsO2 induced HSP-72 in kidney (~50% of standard) and liver (~21% of standard). Neither ethanol nor NaAsO2 alone increased circulating concentrations of IL-1α or TNF-α. However, ethanol given concurrently with endotoxin produced a significant decrease in TNF-α compared to endotoxin alone (p < .01). We conclude that different mechanisms, other than HSPs, are involved in their protective effects against endotoxin.

Original languageEnglish
Pages (from-to)34-39
Number of pages6
JournalShock
Volume2
Issue number1
DOIs
StatePublished - Jul 1994

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