• 1.

    Trumble TN. The use of nutraceuticals for osteoarthritis in horses. Vet Clin North Am Equine Pract 2005;21:575597.

  • 2.

    New Zealand Food Safety Authority. ACVM guideline for good manufacturing practice. Available at: www.nzfsa.govt.nz/acvm/publications/other-standards/manufacturing-standard.pdf. Accessed Mar 4, 2009.

    • Search Google Scholar
    • Export Citation
  • 3.

    New Zealand Food Safety Authority. Revised HACCP standard for HACCP application, HACCP competency. Available at: www.nzfsa.govt.nz/animalproducts/haccp/index.htm. Accessed Mar 4, 2009.

    • Search Google Scholar
    • Export Citation
  • 4.

    Pearson W, Orth MW, Karrow NA, et al. Anti-inflammatory and chondroprotective effects of nutraceuticals in a cartilage explant model of inflammation. Mol Nutr Food Res 2007;51:10201030.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 5.

    Pearson W, Orth MW, Karrow NA, et al. Effects of simulated digests of Biota orientalis and a dietary nutraceutical on interleukin-1–induced inflammatory responses in cartilage explants. Am J Vet Res 2008;69:15601568.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 6.

    Bertone AL, Palmer JL, Jones J. Synovial fluid cytokines and eicosanoids as markers of joint disease in horses. Vet Surg 2001;30:528538.

  • 7.

    Murphy KJ, Mann NJ, Sinclair AJ. Fatty acid and sterol composition of frozen and freeze-dried New Zealand Green Lipped Mussel (Perna canaliculus) from three sites in New Zealand. Asia Pac J Clin Nutr 2003;12:5060.

    • Search Google Scholar
    • Export Citation
  • 8.

    Su XQ, Antonas KN, Li D. Comparison of n-3 polyunsaturated fatty acid contents of wild and cultured Australian abalone. Int J Food Sci Nutr 2004;55:149154.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 9.

    Alencar JW, Pessoa JC, Craveiro AA, et al. Chemical composition of shark cartilage. Rev Bras Farm 1995;76:78.

  • 10.

    Miller TE, Dodd J, Ormrod DJ, et al. Anti-inflammatory activity of glycogen extracted from Perna canaliculus (NZ green-lipped mussel). Agents Actions 1993;38:C139C142.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 11.

    Tingli L, Qin Q, Yi Z, et al. Study on chemical constituents of essential oil of Biota orientalis by GC-MS [in Chinese]. Zhong Yao Cai 2000;23:460461.

    • Search Google Scholar
    • Export Citation
  • 12.

    Curtis CL, Harwood JL, Dent CM, et al. Biological basis for the benefit of nutraceutical supplementation in arthritis. Drug Discov Today 2004;9:165172.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 13.

    Pollard B, Guilford WG, Ankenbauer-Perkins KL, et al. Clinical efficacy and tolerance of an extract of green-lipped mussel (Perna canaliculus) in dogs presumptively diagnosed with degenerative joint disease. N Z Vet J 2006;54:114118.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 14.

    Ghosh P, Shimmon S, Whitehouse MW. Arthritic disease suppression and cartilage protection with glycosaminoglycan polypeptide complexes (Peptacans) derived from the cartilage extracellular matrix: a novel approach to therapy. Inflammopharmacology 2006;14:155162.

    • Search Google Scholar
    • Export Citation
  • 15.

    Yates AC, Stewart AA, Byron CR, et al. Effects of sodium hyaluronate and methylprednisolone acetate on proteoglycan metabolism in equine articular chondrocytes treated with interleukin-1. Am J Vet Res 2006;67:19801986.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 16.

    Frean SP, Cambridge H, Lees P. Effects of anti-arthritic drugs on proteoglycan synthesis by equine cartilage. J Vet Pharmacol Ther 2002;25:289298.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 17.

    Schnyder J, Payne T, Dinarello CA. Human monocyte or recombinant interleukin 1's are specific for the secretion of a metalloproteinase from chondrocytes. J Immunol 1987;138:496503.

    • Search Google Scholar
    • Export Citation
  • 18.

    Inoue K, Masuko-Hongo K, Okamoto M, et al. Induction of vascular endothelial growth factor and matrix metalloproteinase-3 (stromelysin) by interleukin-1 in human articular chondrocytes and synoviocytes. Rheumatol Int 2005;26:9398.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 19.

    McGuire-Goldring MB, Meats JE, Wood DD, et al. In vitro activation of human chondrocytes and synoviocytes by a human interleukin-1-like factor. Arthritis Rheum 1984;27:654662.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 20.

    Blanco FJ, Lotz M. IL-1-induced nitric oxide inhibits chondrocyte proliferation via PGE2. Exp Cell Res 1995;218:319325.

  • 21.

    Fenton JI, Chlebek-Brown KA, Caron JP, et al. Effect of glucosamine on interleukin-1-conditioned articular cartilage. Equine Vet J Suppl 2002;34:219223.

    • Search Google Scholar
    • Export Citation
  • 22.

    DePuy T, Howard R, Keegan K, et al. Effects of intra-articular botulinum toxin type A in an equine model of acute synovitis: a pilot study. Am J Phys Med Rehabil 2007;86:777783.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 23.

    Hardy J, Bertone AL, Weisbrode SE, et al. Cell trafficking, mediator release, and articular metabolism in acute inflammation of innervated or denervated isolated equine joints. Am J Vet Res 1998;59:88100.

    • Search Google Scholar
    • Export Citation
  • 24.

    de Grauw JC, van de Lest CH, van Weeren R, et al. Arthrogenic lameness of the fetlock: synovial fluid markers of inflammation and cartilage turnover in relation to clinical joint pain. Equine Vet J 2006;38:305311.

    • Search Google Scholar
    • Export Citation
  • 25.

    Chandrasekhar S, Esterman MA, Hoffman HA. Microdetermination of proteoglycans and glycosaminoglycans in the presence of guanidine hydrochloride. Anal Biochem 1987;161:103108.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 26.

    Chan PS, Caron JP, Rosa GJ, et al. Glucosamine and chondroitin sulfate regulate gene expression and synthesis of nitric oxide and prostaglandin E(2) in articular cartilage explants. Osteoarthritis Cartilage 2005;13:387394.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 27.

    Steel CM, Hopper BJ, Richardson JL, et al. Clinical findings, diagnosis, prevalence and predisposing factors for lameness localised to the middle carpal joint in young Standardbred race-horses. Equine Vet J 2006;38:152157.

    • Search Google Scholar
    • Export Citation
  • 28.

    Bertone AL, Hardy J, Simmons EJ, et al. Vascular and transsynovial forces of the isolated stationary equine joint. Am J Vet Res 1998;59:495503.

    • Search Google Scholar
    • Export Citation
  • 29.

    Hardy J, Bertone AL, Muir WW III. Local hemodynamics, permeability, and oxygen metabolism during acute inflammation of innervated or denervated isolated equine joints. Am J Vet Res 1998;59:13071316.

    • Search Google Scholar
    • Export Citation
  • 30.

    Simmons EJ, Bertone AL, Hardy J, et al. Nitric oxide synthase activity in healthy and interleukin 1B-exposed equine synovial membrane. Am J Vet Res 1999;60:714716.

    • Search Google Scholar
    • Export Citation
  • 31.

    de la Calle J, Burba DJ, Ramaswamy CM, et al. Plasma and synovial fluid endothelin-1 and nitric oxide concentrations in horses with and without joint disease. Am J Vet Res 2002;63:16481654.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 32.

    Di Mauro D, Bitto L, D'Andrea L, et al. Behaviour of nitric oxide synthase isoforms in inflammatory human joint diseases: an immunohistochemical study. Ital J Anat Embryol 2006;111:111123.

    • Search Google Scholar
    • Export Citation
  • 33.

    Darmani H, Crossan J, McLellan SD, et al. Expression of nitric oxide synthase and transforming growth factor-beta in crush-injured tendon and synovium. Mediators Inflamm 2004;13:299305.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 34.

    Neil KM, Caron JP, Orth MW. The role of glucosamine and chondroitin sulfate in treatment for and prevention of osteoarthritis in animals. J Am Vet Med Assoc 2005;226:10791088.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 35.

    Lee SY, Paik SY, Chung SM. Neovastat (AE-941) inhibits the airway inflammation and hyperresponsiveness in a murine model of asthma. J Microbiol 2005;43:1116.

    • Search Google Scholar
    • Export Citation
  • 36.

    Gingras D, Renaud A, Mousseau N, et al. Matrix proteinase inhibition by AE-941, a multifunctional antiangiogenic compound. Anticancer Res 2001;21:145155.

    • Search Google Scholar
    • Export Citation
  • 37.

    Verde CR, Simpson MI, Villarino N, et al. Therapeutic and hematological effects of native and low molecular weight chondroitin sulphate administered orally in horses with experimental arthritis. Revista Electrónica de Veterinaria REDVET [serial online]. 2006;7:123. Available at: www.veterinaria.org/revistas/redvet/n010106.html. Accessed Jul 25, 2008.

    • Search Google Scholar
    • Export Citation
  • 38.

    Laverty S, Sandy JD, Celeste C, et al. Synovial fluid levels and serum pharmacokinetics in a large animal model following treatment with oral glucosamine at clinically relevant doses. Arthritis Rheum 2005;52:181191.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 39.

    Du J, White N, Eddington ND. The bioavailability and pharmacokinetics of glucosamine hydrochloride and chondroitin sulfate after oral and intravenous single dose administration in the horse. Biopharm Drug Dispos 2004;25:109116.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 40.

    Setnikar I, Rovati LC. Absorption, distribution, metabolism and excretion of glucosamine sulfate. A review. Arzneimittelforschung 2001;51:699725.

    • Search Google Scholar
    • Export Citation
  • 41.

    Kato H, Ohashi T, Nakamura N, et al. Molecular cloning of equine interleukin-1 alpha and -beta cDNAs. Vet Immunol Immunopathol 1995;48:221231.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 42.

    Ebert L, Schick M, Neubert P, et al. Direct submission. (07-MAY-2004) RZPD Deutsches Ressourcenzentrum fuer Genomforschung GmbH Im Neuenheimer Feld 580, D-69120 Heidelberg, Germany.

    • Search Google Scholar
    • Export Citation

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Evaluation of inflammatory responses induced via intra-articular injection of interleukin-1 in horses receiving a dietary nutraceutical and assessment of the clinical effects of long-term nutraceutical administration

Wendy PearsonDepartment of Plant Agriculture, Ontario Agriculture College, University of Guelph, Guelph, ON N1G 2W1, Canada.

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Michael W. OrthDepartment of Animal Science, College of Agriculture and Natural Resources, Michigan State University, East Lansing, MI 48824.

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Michael I. LindingerDepartment of Human Health and Nutritional Sciences, College of Biological Sciences, University of Guelph, Guelph, ON N1G 2W1, Canada.

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Abstract

Objective—To evaluate inflammatory responses induced via intra-articular recombinant human interleukin (IL)-1β treatment in horses receiving a dietary nutraceutical (DN; composed of mussel, shark cartilage, abalone, and Biota orientalis lipid extract) and assess the clinical effects of long-term DN administration.

Animals—22 healthy horses.

Procedures—12 horses were fed 0, 15, 45, or 75 mg of DN (3 horses/treatment) daily for 84 days. General health and clinicopathologic variables were monitored at intervals. Ten other horses received 0 or 15 g of DN/d (5 horses/treatment) for 29 days (beginning day −14). One intercarpal joint in each horse was injected twice with IL-1β (10 and 100 ng on days 0 and 1, respectively), and the contralateral joint was similarly injected with saline (0.9% NaCl) solution. Synovial fluid prostaglandin E2 (PGE2), sulfated glycosaminoglycan (GAG), nitric oxide (NO), and protein concentrations and leukocyte counts were analyzed before and at intervals after injections.

Results—Administration of the DN (up to 75 g/d) to horses for 84 days did not induce any adverse effects. In the other experiment, synovial fluid PGE2, GAG, and protein concentrations and leukocyte count increased after intra-articular injections of IL-1β (compared with effects of saline solution injections) in horses that received no DN; NO concentration was not affected. In horses that were fed the DN, intra-articular IL-1β injections did not induce significant increases in synovial fluid PGE2 and GAG concentrations.

Conclusions and Clinical Relevance—Results suggested that administration of the DN may be useful in preventing inflammation associated with arthritis and degenerative joint disease in horses.

Abstract

Objective—To evaluate inflammatory responses induced via intra-articular recombinant human interleukin (IL)-1β treatment in horses receiving a dietary nutraceutical (DN; composed of mussel, shark cartilage, abalone, and Biota orientalis lipid extract) and assess the clinical effects of long-term DN administration.

Animals—22 healthy horses.

Procedures—12 horses were fed 0, 15, 45, or 75 mg of DN (3 horses/treatment) daily for 84 days. General health and clinicopathologic variables were monitored at intervals. Ten other horses received 0 or 15 g of DN/d (5 horses/treatment) for 29 days (beginning day −14). One intercarpal joint in each horse was injected twice with IL-1β (10 and 100 ng on days 0 and 1, respectively), and the contralateral joint was similarly injected with saline (0.9% NaCl) solution. Synovial fluid prostaglandin E2 (PGE2), sulfated glycosaminoglycan (GAG), nitric oxide (NO), and protein concentrations and leukocyte counts were analyzed before and at intervals after injections.

Results—Administration of the DN (up to 75 g/d) to horses for 84 days did not induce any adverse effects. In the other experiment, synovial fluid PGE2, GAG, and protein concentrations and leukocyte count increased after intra-articular injections of IL-1β (compared with effects of saline solution injections) in horses that received no DN; NO concentration was not affected. In horses that were fed the DN, intra-articular IL-1β injections did not induce significant increases in synovial fluid PGE2 and GAG concentrations.

Conclusions and Clinical Relevance—Results suggested that administration of the DN may be useful in preventing inflammation associated with arthritis and degenerative joint disease in horses.

Contributor Notes

Supported by Interpath Pty Ltd, Australia, and the Natural Sciences and Engineering Research Council (NSERC) of Canada.

Dr. Pearson was supported by a scholarship from NSERC.

The study sponsor did not participate in the study design; collection, analysis, or interpretation of data; writing of the manuscript; or the decision to submit the manuscript for publication.

The authors thank Drs. Dan Kenney and Antonio Cruz for technical assistance regarding arthrocentesis procedures.

Address correspondence to Dr. Pearson.