Critical Care

official impact factor 4.60

This article is part of the supplement: Sepsis 2009

Poster presentation

Muscimol increases the survival rate and inhibits the inflammatory response in endotoxemic mice

D-Z Hsu*, Y-H Li, P-Y Chu and M-Y Liu

  • * Corresponding author: D-Z Hsu

Author Affiliations

Department of Environmental and Occupational Health, National Cheng Kung University Medical College, Tainan, Taiwan, Republic of China

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Critical Care 2009, 13(Suppl 4):P19 doi:10.1186/cc8075


The electronic version of this article is the complete one and can be found online at: http://ccforum.com/content/13/S4/P19


Published:11 November 2009

© 2009 BioMed Central Ltd.

Introduction

Affecting the γ-amino butyric acid (GABA) pathway results in an alteration of inflammatory response in various animal models. However, its mechanism is still unclear. The aim of this study was to determine the effects of muscimol, a GABAA receptor agonist, on lipopolysaccharide-induced mortality and inflammation in mice.

Materials

C57BL6 mice, lipopolysaccharide (derived from Escherichia coli, serotype O55:B5), and muscimol were used in this study.

Methods

Mice endotoxemia was induced by 10 mg/kg lipopolysaccharide intraperitoneally. Muscimol ranging from 0 to 3 mg/kg were given subcutaneously 30 minutes before lipopolysaccharide administration. Serum TNFα, IL-1β, IL-10, and IL-12 were determined using ELISA.

Results

Muscimol significantly increased the survival rate in sub-lethal dose of lipopolysaccharide-treated mice (from 7% to 100%) (P < 0.0001) within 72 hours. Muscimol inhibited serum TNFα, IL-1β, and IL-12 production in a dose-dependent manner. Furthermore, muscimol significantly increased serum IL-10 levels (P < 0.001) in lipopolysaccharide-treated mice.

Conclusion

Muscimol potently increased the survival rate and inhibited inflammatory response in endotoxemic mice.