Critical timing, location and duration of glucocorticoid administration rescue mice from superantigen-induced shock and attenuate lung injury

Int Immunopharmacol. 2009 Sep;9(10):1168-74. doi: 10.1016/j.intimp.2009.06.004. Epub 2009 Jun 16.

Abstract

Bacterial superantigens, such as staphylococcal enterotoxin B (SEB), are major virulence factors implicated in the pathogenesis of toxic shock. In this study we investigated the efficacy of glucocorticoid therapy in preventing SEB-induced lethal shock initiated through the respiratory route in mice. Dexamethasone, a potent anti-inflammatory steroid, administrated intranasally on the first day, followed by intraperitoneal doses on the subsequent 4 days, was effective in attenuating SEB-induced hypothermia, and reduction in systemic and pulmonary proinflammatory mediator release. This optimal dosing and schedule of glucocorticoid treatment mitigated lung inflammation and resulted in 100% survival in this intranasal mouse model of SEB-mediated shock.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / administration & dosage*
  • Cytokines / blood
  • Dexamethasone / administration & dosage*
  • Drug Administration Routes
  • Enterotoxins / immunology
  • Lung / drug effects*
  • Lung / immunology
  • Lung / metabolism
  • Lung / pathology
  • Male
  • Mice
  • Mice, Inbred C3H
  • Shock, Septic / drug therapy*
  • Shock, Septic / immunology
  • Shock, Septic / pathology
  • Shock, Septic / physiopathology
  • Staphylococcal Infections / drug therapy*
  • Staphylococcal Infections / immunology
  • Staphylococcal Infections / pathology
  • Staphylococcal Infections / physiopathology
  • Staphylococcus / immunology*
  • Time Factors

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Enterotoxins
  • enterotoxin B, staphylococcal
  • Dexamethasone