The anti-inflammatory effect of the extract of Ruta chalepensis L. (Rutaceae) on the course of lethal endotoxemia in BALB/c mice was studied. When administered by gavage as 1 g/kg/day starting 14 or 7 days prior to injection of 0.75 mg endotoxin (LPS: lypopolisaccharide), the extract markedly reduced lethality (32.5% in both experiments vs approximately 85% of the control mice). A delay in lethality, but not cumulative lethality, was observed when prophylaxis was given 24 and 1 h prior to LPS-challenge. The effect was associated with reduced LPS-induced blood levels of nitrite, an indicator of nitric oxide production. In contrast, the blood levels of tumour necrosis factor, interleukin 6 and interleukin 10 did not differ significantly from those of controls given LPS alone. These data show that R. chalepensis L. possesses powerful immunopharmacological properties that make it capable of counteracting the lethal effects of high doses of LPS in vivo.

Protection against murine endotexemia by treatment with Ruta chalepensis L

RAGUSA S;
2004-01-01

Abstract

The anti-inflammatory effect of the extract of Ruta chalepensis L. (Rutaceae) on the course of lethal endotoxemia in BALB/c mice was studied. When administered by gavage as 1 g/kg/day starting 14 or 7 days prior to injection of 0.75 mg endotoxin (LPS: lypopolisaccharide), the extract markedly reduced lethality (32.5% in both experiments vs approximately 85% of the control mice). A delay in lethality, but not cumulative lethality, was observed when prophylaxis was given 24 and 1 h prior to LPS-challenge. The effect was associated with reduced LPS-induced blood levels of nitrite, an indicator of nitric oxide production. In contrast, the blood levels of tumour necrosis factor, interleukin 6 and interleukin 10 did not differ significantly from those of controls given LPS alone. These data show that R. chalepensis L. possesses powerful immunopharmacological properties that make it capable of counteracting the lethal effects of high doses of LPS in vivo.
2004
Ruta chalepensis; Endotoxemia; Anti-inflammatory properties
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.12317/10582
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