Article ID Journal Published Year Pages File Type
2541763 International Immunopharmacology 2009 5 Pages PDF
Abstract

Florfenicol, an antibiotic used to treat infection, has previously been shown to modulate early cytokine responses and increase mouse survival in endotoxemia. In the present study, we investigated in vivo the effect of florfenicol on acute lung injury (ALI) induced by lipopolysaccharide (LPS). In the mouse model of LPS-induced inflammatory lung injury, we found that pretreatment with a single 100 mg/kg dose of florfenicol significantly decreases the W/D ratio of lungs and protein concentration in the bronchoalveolar lavage fluid (BALF) and significantly reduces the number of total cells, neutrophils and macrophages in the BALF at 24 h after LPS challenge. In addition, histopathological examination indicates that florfenicol significantly attenuates tissue injury of the lungs in LPS-induced ALI. Furthermore, florfenicol also inhibits the production of several inflammatory cytokines, including tumor necrosis factor-α (TNF-α) at 6 and 12 h, interleukin-6 (IL-6) at 12 and 24 h, and interleukin-1ß (IL-1ß) at 12 h, in the BALF after LPS challenge. These results suggest that florfenicol protects against LPS-induced ALI in mice.

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