Benznidazole, a drug used in Chagas'disease, ameliorates LPS induced inflammatory response in mice

PASCUTTI MF; PITASHNY M; NOCITO A; GUERMONPREZ G; AMIGORENA S; WIETZERBIN J; SERRA E; BOTTASSO O; REVELLI S; BOTTASSO OSCAR

LIFE SCIENCES

PERGAMON-ELSEVIER SCIENCE LTD

Lugar: Estocolmo; Año: 2004 vol. 76 p. 685 - 697

0024-3205

Benznidazole (BZL) is a drug currently used for treating Chagas? disease. Given our earlier demonstration in which BZL downregulated cytokine and nitric oxide (NO) synthesis by LPS and/or IFN-g-stimulated murine macrophages, we have now analysed whether this compound could exert beneficial effects in a model of LPS-induced inflammation in C57BL/6 mice. The lethal model consisted of two LPS intraperitoneal injections, 200 Ag each separated by 2 h, with BZL given orally at a dose of 200 mg/kg, 18 and 2 h before the first challenge and 20 and 44 hr following the second one. In this model, BZL treatment led to a significantly decreased mortality in comparison with untreated counterparts. Remainingexperiments were carried out in mice given a unique LPS dose, pretreated with BZL or not, since those subjected to the lethal protocol were unsuitable for laboratory handling. Analysis of IL-1h, IL-6, TNF-a, IL-12 and iNOS mRNA expression in liver samples taken at 90 min post-LPS showed a marked reduction of the two latter mRNAs in BZL-treated mice. These animals also displayed significantly decreased peaks levels of serum TNF-a and IL-6, accompanied by a diminished number of IL-6-producing peritoneal macrophages.