1. Therapeutic and preventive properties of quercetin in experimental arthritis correlate with decreased macrophage inflammatory mediators
- Author
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Jérôme Rambert, Sara Coves, Daniel Moynet, M. Djavad Mossalayi, Tina Kauss, Denis Thiolat, Denis Malvy, Maria Mamani-Matsuda, Abir Al-Kharrat, and Fawaz Fawaz
- Subjects
Injections, Intradermal ,Administration, Oral ,Nitric Oxide Synthase Type II ,Arthritis ,Inflammation ,Pharmacology ,Biochemistry ,Nitric oxide ,chemistry.chemical_compound ,In vivo ,Oral administration ,medicine ,Animals ,business.industry ,Anti-Inflammatory Agents, Non-Steroidal ,Pentahydroxyflavone ,medicine.disease ,Arthritis, Experimental ,Rats ,chemistry ,Rats, Inbred Lew ,Immunology ,Macrophages, Peritoneal ,Female ,Quercetin ,Tumor necrosis factor alpha ,Inflammation Mediators ,medicine.symptom ,business ,Ex vivo - Abstract
Pentahydroxyflavone dihydrate, quercetin (QU) is one of common flavonols biosynthesized by plants and has been suggested to modulate inflammatory responses in various models. In the present study, we investigated in vivo effects of oral or intra-cutaneous QU in chronic rat adjuvant-induced arthritis (AA). Growth delay and arthritic scores were evaluated daily after AA induction in Lewis rats. Oral administration of QU (5 x 160 mg/kg) to arthritic rats resulted in a clear decrease of clinical signs compared to untreated controls. Intra-cutaneous injections of lower doses (5 x 60 mg/kg) of QU gave similar anti-arthritic effects, while 5 x 30 mg/kg concentrations were inefficient in this respect. Finally, injection of relatively low QU doses (5 x 30 mg/kg) prior to AA induction significantly reduced arthritis signs. As QU was suggested to inhibit macrophage-derived cytokines and nitric oxide (NO), we then analyzed macrophage response ex vivo. Anti-arthritic effects of QU correlated with significant decrease of inflammatory mediators produced by peritoneal macrophages, ex vivo and in vitro. These data indicate that QU is a potential anti-inflammatory therapeutic and preventive agent targeting the inflammatory response of macrophages.
- Published
- 2006
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