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Inhibition of monosodium urate crystal-induced inflammation by withaferin A
E.P. Sabina, S. Chandel,
Published in Canadian Society for Pharmaceutical Sciences
2008
PMID: 19183513
Volume: 11
   
Issue: 4
Pages: 46 - 55
Abstract
Purpose. Gouty arthritis is a characteristically intense acute inflammatory reaction resulting from the formation of sodium urate crystals in the joint cavity. In the present study, the effect of withaferin A, a steroidal lactone was investigated on monosodium urate crystalinduced inflammation in mice; an experimental model for gouty arthritis and compared it with that of the non-steroidal anti-inflammatory drug, indomethacin. Methods. Paw volume and levels/activities of lysosomal enzymes, lipid peroxidation, anti-oxidant status and inflammatory mediator TNF-α were determined in control and monosodium urate crystal-induced mice. The levels of β;-glucuronidase and lactate dehydrogenase were also measured in monosodium urate crystalincubated polymorphonuclear leucocytes (PMNL). Results. Paw volume, the levels of lysosomal enzymes, lipid peroxidation, and inflammatory mediator tumour necrosis factor-a were found to be increased significantly and the activities of antioxidant status were in turn decreased in monosodium urate crystal-induced mice; however these changes were reverted back to near normal levels in withaferin A (30 mg/kg/b.wt, i.p.) treated monosodium urate crystal-induced mice. In addition, ß-glucuronidase and lactate dehydrogenase level were reduced in withaferin A (50/100μg/ml) treated monosodium urate crystalincubated polymorphonuclear leucocytes. Conclusion. The present findings clearly indicated that withaferin A exerted a strong antiinflammatory effect against gouty arthritis.
About the journal
JournalJournal of Pharmacy and Pharmaceutical Sciences
PublisherCanadian Society for Pharmaceutical Sciences
ISSN14821826