Key result
Resveratrol significantly reduced the expression of MMP-1 (p=0.022), MMP-3 (p=0.021), MMP-9 (p=0.047), OPG (p=0.012), and RANKL (p=0.018) in interleukin-1beta-stimulated RA-FLS.
Why the study?
Does resveratrol reduce the expression of matrix-degrading enzymes and bone-remodelling proteins in interleukin-1beta-stimulated rheumatoid arthritis fibroblast-like synoviocytes?
Does resveratrol reduce the expression of matrix-degrading enzymes and bone-remodelling proteins in interleukin-1beta-stimulated rheumatoid arthritis fibroblast-like synoviocytes?
p-value: p=0.022
Resveratrol reduces the expression of matrix metalloproteinases and RANKL in rheumatoid arthritis fibroblast-like synoviocytes in vitro, indicating potential chondro-protective properties.
May modulate RA joint destruction pathways in vitro; hypothesis-generating and requires clinical trials before any therapeutic consideration.
Medication of rheumatoid arthritis (RA) remains challenging and often controversial concerning side effects or long-term complications. We investigated the effect of resveratrol, a phytoalexin discussed for its chondro-protective and anti-inflammatory qualities, on the synovial expression of matrix-degrading enzymes like matrix metalloproteinases (MMPs) and bone-remodelling proteins in RA fibroblast-like synoviocytes (FLS). Interleukin-1beta-stimulated RA-FLS were treated with 100 microM resveratrol for 24 h. To evaluate the effect of resveratrol on the amount of bound/combined MMPs, a Luminex xMAP multiplexing technology was used. The alteration in expression of receptor activator of nuclear factor-kappaB ligand (RANKL) and osteoprotegrin (OPG) was measured by quantitative real-time polymerase chain reaction (qRT-PCR). Resveratrol reduced the expression of MMP-1 (p = 0.022), MMP-3 (p = 0.021), and MMP-9 (p = 0.047). qRT-PCR showed a significant reduction in the relative abundance of the transcripts of OPG (p = 0.012) and RANKL (p = 0.018). Our in vitro findings indicate that resveratrol could be a new target for further pharmacological studies in the field of RA. In the future it could play a role as a possible substitute or supplement to currently used drugs against RA to prevent cartilage matrix degradation and pathological bone resorption due to inhibition of MMPs and RANKL.
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Glehr et al. (2013) studied Rheumatoid arthritis. Resveratrol was evaluated on Expression of MMP-1 (p=0.022). Resveratrol significantly reduced the expression of MMP-1 (p=0.022), MMP-3 (p=0.021), MMP-9 (p=0.047), OPG (p=0.012), and RANKL (p=0.018) in interleukin-1beta-stimulated RA-FLS.
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