Osteoarthritis and Cartilage
Volume 19, Issue 9 , Pages 1150-1157, September 2011

Regulation of osteoarthritis by omega-3 (n-3) polyunsaturated fatty acids in a naturally occurring model of disease

  • L. Knott

      Affiliations

    • Matrix Biology, Div. VPII, University of Bristol, Veterinary School, Langford, Bristol BS40 5DU, UK
  • ,
  • N.C. Avery

      Affiliations

    • Matrix Biology, Div. VPII, University of Bristol, Veterinary School, Langford, Bristol BS40 5DU, UK
  • ,
  • A.P. Hollander

      Affiliations

    • Stem Cell Biology, Cellular and Molecular Medicine, University of Bristol, Bristol BS8 1TD, UK
  • ,
  • J.F. Tarlton

      Affiliations

    • Matrix Biology, Div. VPII, University of Bristol, Veterinary School, Langford, Bristol BS40 5DU, UK
    • Corresponding Author InformationAddress correspondence and reprint requests to: J.F. Tarlton, Matrix Biology, Div. VPII, University of Bristol, Veterinary School, Langford, Bristol BS40 5DU, UK. Tel: 44-117-9289266; Fax: 44-117-9289505.

Received 25 October 2010; accepted 9 June 2011. published online 11 July 2011.

Summary 

Objective

To examine effects of high omega-3 (n-3) polyunsaturated fatty acid (PUFA) diets on development of osteoarthritis (OA) in a spontaneous guinea pig model, and to further characterise pathogenesis in this model. Modern diets low in n-3 PUFAs have been linked with increases in inflammatory disorders, possibly including OA. However, n-3 is also thought to increases bone density, which is a possible contributing factor in OA. Therefore we aim to determine the net influence of n-3 in disease development.

Method

OA-prone Dunkin-Hartley (DH) Guinea pigs were compared with OA-resistant Bristol Strain-2s (BS2) each fed a standard or an n-3 diet from 10 to 30weeks (10/group). We examined cartilage and subchondral bone pathology by histology, and biochemistry, including collagen cross-links, matrix metalloproteinases (MMPs), alkaline phosphatase, glycosaminoglycan (GAG), and denatured type II collagen.

Results

Dietary n-3 reduced disease in OA-prone animals. Most cartilage parameters were modified by n-3 diet towards those seen in the non-pathological BS2 strain – significantly active MMP-2, lysyl-pyridinoline and total collagen cross-links – the only exception being pro MMP-9 which was lower in the BS2, yet increased with n-3. GAG content was higher and denatured type II lower in the n-3 group. Subchondral bone parameters in the DH n-3 group also changed towards those seen in the non-pathological strain, significantly calcium:phosphate ratios and epiphyseal bone density.

Conclusion

Dietary n-3 PUFA reduced OA in the prone strain, and most disease markers were modified towards those of the non-OA strain, though not all significantly so. Omega-3 did not increase markers of pathology in either strain.

Keywords: Osteoarthritis, Polyunsaturated fatty acids, Guinea pig model, Cartilage, Subchondral bone

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PII: S1063-4584(11)00164-6

doi:10.1016/j.joca.2011.06.005

Osteoarthritis and Cartilage
Volume 19, Issue 9 , Pages 1150-1157, September 2011