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Efficacy of two FDA-approved drug combination in a mouse model of staphylococcal enterotoxin B-induced shock.

Abstract
Staphylococcal enterotoxin B (SEB) causes lethal shock by potently stimulating the host immune response. Dexamethasone and N-acetyl cysteine (NAC) are anti-inflammatory and antioxidative drugs, respectively, which can independently modulate immune function. Dexamethasone was previously shown to be effective in preventing SEB-induced shock models only if administered early and in multiple doses for a long duration. In this study, dexamethasone and NAC were used in tandem and protected mice (75%) against SEB-induced lethal shock. Hypothermia and weight loss elicited by SEB were also diminished by this novel combination treatment. The levels of monocyte chemoattractant protein-1, interleukin-2, interleukin-6, and mouse gamma interferon in lung tissue after intranasal exposure to SEB were also significantly reduced in mice given a combination of dexamethasone and NAC versus controls.
AuthorsTeresa Krakauer, Marilyn Buckley
JournalMilitary medicine (Mil Med) Vol. 178 Issue 9 Pg. 1024-8 (Sep 2013) ISSN: 1930-613X [Electronic] England
PMID24005553 (Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S.)
CopyrightReprint & Copyright © 2013 Association of Military Surgeons of the U.S.
Chemical References
  • Anti-Inflammatory Agents
  • Chemokine CCL2
  • Enterotoxins
  • Free Radical Scavengers
  • Interleukin-2
  • Interleukin-6
  • enterotoxin B, staphylococcal
  • Dexamethasone
  • Interferon-gamma
  • Acetylcysteine
Topics
  • Acetylcysteine (therapeutic use)
  • Animals
  • Anti-Inflammatory Agents (therapeutic use)
  • Chemokine CCL2 (metabolism)
  • Dexamethasone (therapeutic use)
  • Disease Models, Animal
  • Drug Therapy, Combination
  • Enterotoxins
  • Female
  • Free Radical Scavengers (therapeutic use)
  • Interferon-gamma (metabolism)
  • Interleukin-2 (metabolism)
  • Interleukin-6 (metabolism)
  • Lung (metabolism)
  • Male
  • Mice
  • Shock, Septic (blood, chemically induced, drug therapy)

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