AI Article Synopsis

  • An inverse relationship exists between rheumatoid arthritis severity and β-cryptoxanthin intake, indicating potential protective effects.
  • Oral administration of β-cryptoxanthin to arthritic rats reduced cartilage degradation by inhibiting enzymes that break down a key cartilage protein, aggrecan.
  • In cell cultures, β-cryptoxanthin not only decreased harmful gene expression related to cartilage breakdown but also promoted the production of cartilage building blocks, suggesting it may help manage arthritis progression.

Article Abstract

An inverse correlation between the morbidity of rheumatoid arthritis and daily intake of β-cryptoxanthin has been epidemiologically shown. In this study, we investigated the effects of β-cryptoxanthin on the metabolism of cartilage extracellular matrix in vivo and in vitro. Oral administration of β-cryptoxanthin (0.1-1 mg/kg) to antigen-induced arthritic rats suppressed the loss of glycosaminoglycans in articular cartilage, which is accompanied by the interference of aggrecanase-mediated degradation of aggrecan. Inhibition of the interleukin 1α (IL-1α)-induced aggrecan degradation by β-cryptoxanthin was also observed with porcine articular cartilage explants in culture. β-Cryptoxanthin (1-10 μM) dose-dependently down-regulated the IL-1α-induced gene expression of aggrecanase 1 (ADAMTS-4) and aggrecanase 2 (ADAMTS-5) in cultured human chondrocytes. Moreover, β-cryptoxanthin was found to augment the gene expression of aggrecan core protein in chondrocytes. These results provide novel evidence that β-cryptoxanthin exerts anti-arthritic actions and suggest that β-cryptoxanthin may be useful in blocking the progression of rheumatoid arthritis and osteoarthritis.

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Source
http://dx.doi.org/10.1016/j.bbrc.2016.05.126DOI Listing

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