Journal
INTERNATIONAL IMMUNOPHARMACOLOGY
Volume 14, Issue 2, Pages 157-163Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.intimp.2012.07.001
Keywords
7, 3 '-dimethoxy hesperetin; Adjuvant arthritis; IL-6; JAK2-STAT3 signal pathway
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Funding
- National Natural Science Foundation of China [81102273]
- Specialized Research Fund for the Doctoral Program of Higher Education [20113420120005]
- Anhui Provincial Natural Science Foundation [11040606Q15]
- Anhui Medical University [XJ201020]
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In our previous study, we have demonstrated that 7, 3'-dimethoxy hesperetin (DMHP), an active derivative of hesperidin, showed pro-apoptotic effect on synoviocytes in vitro. The present study was to investigate the potential therapeutic effect of DMHP on adjuvant arthritis (AA) in rat and its possible mechanisms. Freund's complete adjuvant was used to induce M in rats. DMHP were administered intragastrically once a day from days 12 to 21 after AA induction. Secondary paw swelling, arthritis index, and pathological assessments were observed. IL-6 production in serum and IL-6 mRNA expression in synovium was detected by ELISA and real-time RT-PCR respectively. The expression of mRNA (JAK2, STAT3) and protein (JAK2, p-JAK2, STAT3, p-STAT3) in synovium were determined. We found that DMHP significantly inhibited hind paw swelling and arthritis index, and ameliorated pathological changes of ankle joint in AA rats. DMHP suppressed the level of IL-6 in serum and the expression of IL-6 mRNA in synovium of M rats in a dose-dependent manner. DMHP apparently decreased mRNA expression of JAK2 and STAT3 as well as protein expression of p-JAK2 and p-STAT3 in the synovium of the AA rats. Correlation analysis indicated that p-JAK2 or p-STAT3 protein expression was highly correlated with joint damage severity. In conclusion, DMHP has a powerful therapeutic effect on AA in rats and its mechanisms might be partly related to inhibiting excessive activation of JAK2-STAT3 pathway. (C) 2012 Elsevier B.V. All rights reserved.
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