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Translational animal science2020; 4(2); txaa006; doi: 10.1093/tas/txaa006

Evaluation of dietary trace mineral supplementation in young horses challenged with intra-articular lipopolysaccharide.

Abstract: Sixteen weanling Quarter Horses (255 ± 22 kg) were utilized in a 56-d trial to evaluate the effects of trace mineral (TM) source on intra-articular inflammation following a single acute inflammatory insult. Horses were stratified by age, sex, and BW and then randomly assigned to dietary treatment: concentrate formulated with Zn, Mn, Cu, and Co as inorganic sources (CON; n = 8) or complexed TMs (CTM; n = 8). Added TM were formulated at iso-levels across treatments and intakes met or exceeded NRC requirements. Horses were offered 1.75% BW (as-fed) of treatment concentrate and 0.75% BW (as-fed) coastal Bermudagrass hay. Growth measurements were collected on days 0, 28, and 56, and plasma was collected biweekly for determination of Mn, Cu, Zn, and Co concentrations. On day 42, carpal joints were randomly assigned to receive injections of 0.5 ng lipopolysaccharide (LPS) or sterile lactated Ringer's solution (LRS; contralateral control). Synovial fluid was collected at preinjection hours (PIH) 0, and 6, 12, 24, 168, and 336 h post-injection and analyzed for TM concentration, prostaglandin E2 (PGE2), carboxypeptide of type II collagen (CPII), collagenase cleavage neopeptide (C2C), and aggrecan chondroitin sulfate 846 epitope (CS846). Data were analyzed using the MIXED procedure of SAS. Results showed a TM source × LPS × h effect for synovial fluid Co, Cu, and Se (P < 0.05); concentrations of TM peaked at hour 6 and decreased to preinjection values by hour 168 in both CON and CTM-LPS knees. A delayed peak was observed at hour 12 for CTM-LRS. Peak synovial fluid Cu and Se concentrations were higher in LPS knees, and Co was highest in CTM-LPS. A TM source × h interaction was observed for Zn (P < 0.05); concentrations peaked at hour 6 in CON vs. hour 12 for CTM. An LPS × h interaction was observed for Mn (P < 0.01); synovial concentration peaked at hour 6 in LPS knees compared with hour 24 in LRS. Synovial PGE2, C2C, CPII, and CS846 concentrations were greater with LPS (P ≤ 0.01), and C2C was greater (P < 0.01) in CTM compared with CON. Concentrations of CPII and PGE2 were unaffected by diet. A TM source × h × LPS interaction was observed for CS846 (P = 0.02). Concentrations of CS846 in CTM peaked at 12 h, whereas CON peaked at a lower concentration at 24 h (P < 0.05). Data indicate sufficient intake of a complexed TM source may support cartilage metabolism through increased aggrecan synthesis and type II collagen breakdown following an intra-articular LPS challenge in growing horses.
Publication Date: 2020-01-17 PubMed ID: 32705007PubMed Central: PMC7001113DOI: 10.1093/tas/txaa006Google Scholar: Lookup
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  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research article investigates the effect of dietary trace mineral (TM) supplementation on young horses subjected to a single inflammatory stimulus. This study is critical as it helps understand how TM can support cartilage metabolism, healing, and growth.

Experimental Methodology

  • The study involved sixteen weanling Quarter Horses, each weighing about 255 ± 22 kg. These horses were part of a 56-day trial designed to examine the influence of TM source on intra-articular inflammation following an acute inflammatory insult.
  • Horses were divided by age, sex, and body weight (BW) and then randomly assigned to a dietary treatment. The treatments contained Zinc (Zn), Manganese (Mn), Copper (Cu), and Cobalt (Co), either as inorganic sources (CON) or as complexed TMs (CTM).
  • The researchers implemented dietary control for all the horses. They were fed a diet of a treatment concentrate and coastal Bermudagrass hay which met or exceeded NRC requirements.
  • On the 42nd day, the researchers injected carpal joints with lipopolysaccharide (LPS) or sterile lactated Ringer’s solution (LRS; contralateral control). Synovial fluid was collected at different time points following the injection and analyzed for TM concentration, prostaglandin E (PGE), carboxypeptide of type II collagen (CPII), collagenase cleavage neopeptide (C2C), and aggrecan chondroitin sulfate 846 epitope (CS846).

Findings of the Study

  • The study found that trace minerals peaked at the 6th hour after the LPS injection and reduced to preinjection values by the 168th hour in both the CON and CTM-LPS knee groups. In the CTM-Lactated Ringer’s Solution group, the peak in minerals was delayed until the 12th hour.
  • A more significant increase in synovial fluid Cu and Se concentrations were observed in the LPS-injected knees, and Co was highest in the CTM-LPS group.
  • For Zn, the peak concentration occurred at the 6th hour in CON, while it was delayed till the 12th hour in CTM.
  • When observing Mn, the peak synovial concentration occurred at the 6th hour in LPS knees compared to the 24th hour in LRS.
  • Higher Synovial PGE, C2C, CPII, and CS846 concentrations were observed with LPS, and C2C was higher in CTM compared with CON. The CPII and PGE concentrations, however, were unaffected by diet.
  • Finally, a significant interaction was detected for CS846. In the CTM group, concentrations of CS846 peaked at 12 hours, whereas in the CON group, the peak was at 24 hours but at a lower concentration.

Conclusion

Based on the observations, the researchers concluded that an adequate intake of a complexed trace mineral source could support cartilage metabolism — particularly increases in aggrecan synthesis and type II collagen breakdown — after an intra-articular LPS challenge in growing horses. This finding holds significant implications for horse healthcare and diet planning, especially in managing inflammation and maintaining cartilage health.

Cite This Article

APA
Millican AA, Leatherwood JL, Coverdale JA, Arnold CE, Bradbery AN, Larson CK, Lamprecht ED, White SH, Paulk CB, Welsh TH, Wickersham TA. (2020). Evaluation of dietary trace mineral supplementation in young horses challenged with intra-articular lipopolysaccharide. Transl Anim Sci, 4(2), txaa006. https://doi.org/10.1093/tas/txaa006

Publication

ISSN: 2573-2102
NlmUniqueID: 101738705
Country: England
Language: English
Volume: 4
Issue: 2
Pages: txaa006

Researcher Affiliations

Millican, Allison A
  • Department of Animal Science, Texas A&M University, College Station, TX.
Leatherwood, Jessica L
  • Department of Animal Science, Texas A&M University, College Station, TX.
Coverdale, Josie A
  • Department of Animal Science, Texas A&M University, College Station, TX.
Arnold, Carolyn E
  • Department of Large Animal Clinical Sciences, Texas A&M University, College Station, TX.
Bradbery, Amanda N
  • Department of Animal Science, Texas A&M University, College Station, TX.
Larson, Connie K
  • Zinpro Corporation, Eden Prairie, MN.
Lamprecht, Emily D
  • Cargill Animal Nutrition, Elk River, MN.
White, Sarah H
  • Department of Animal Science, Texas A&M University, College Station, TX.
Paulk, Chad B
  • Department of Grain Science and Industry, Kansas State University, Manhattan, KS.
Welsh, Thomas H
  • Department of Animal Science, Texas A&M University, College Station, TX.
Wickersham, Tryon A
  • Department of Animal Science, Texas A&M University, College Station, TX.

References

This article includes 36 references
  1. AOAC 2019. Official methods of analysis. 21st ed. Gaithersburg, MD: Assoc. Off. Anal. Chem.
  2. Bertone AL, Palmer JL, Jones J. Synovial fluid cytokines and eicosanoids as markers of joint disease in horses. Vet. Surg. 30:528–538.
    doi: 10.1053/jvet.2001.28430pubmed: 11704948google scholar: lookup
  3. Blake DR, Hall ND, Treby DA, Halliwell B, Gutteridge JM. Protection against superoxide and hydrogen peroxide in synovial fluid from rheumatoid patients. Clin. Sci. (Lond.) 61:483–486.
    doi: 10.1042/cs0610483pubmed: 7285498google scholar: lookup
  4. Cheng T, Guo Y. Effects of Salmonella typhymurium lipopolysaccharide challenge on the performance, immune responses and zinc metabolism of laying hens supplemented with two zinc sources. Asian-Aust. J. Anim. Sci. 17:1717–1724.
  5. de Grauw JC, Donabédian M, van de Lest CH, Perona G, Robert C, Lepage O, Martin-Rosset W, van Weeren PR. Assessment of synovial fluid biomarkers in healthy foals and in foals with tarsocrural osteochondrosis. Vet. J. 190:390–395.
    doi: 10.1016/j.tvjl.2010.12.001pubmed: 21216637google scholar: lookup
  6. de Grauw JC, van de Lest CH, Brama PA, Rambags BP, van Weeren PR. In vivo effects of meloxicam on inflammatory mediators, MMP activity and cartilage biomarkers in equine joints with acute synovitis. Equine Vet. J. 41:693–699.
    doi: 10.2746/042516409x436286pubmed: 19927589google scholar: lookup
  7. de Grauw JC, van de Lest CH, van Weeren R, Brommer H, Brama PA. Arthrogenic lameness of the fetlock: synovial fluid markers of inflammation and cartilage turnover in relation to clinical joint pain. Equine Vet. J. 38:305–311.
    doi: 10.2746/042516406777749236pubmed: 16866196google scholar: lookup
  8. Favero A, Vieira SL, Angel CR, Bos-Mikich A, Lothhammer N, Taschetto D, Cruz RF, Ward TL. Development of bone in chick embryos from Cobb 500 breeder hens fed diets supplemented with zinc, manganese, and copper from inorganic and amino acid-complexed sources. Poult. Sci. 92:402–411.
    doi: 10.3382/ps.2012-02670pubmed: 23300307google scholar: lookup
  9. Frisbie DD, Al-Sobayil F, Billinghurst RC, Kawcak CE, McIlwraith CW. Changes in synovial fluid and serum biomarkers with exercise and early osteoarthritis in horses. Osteoarthr. Cartilage 16:1196–1204.
    doi: 10.1016/j.joca.2008.03.008pubmed: 18442931google scholar: lookup
  10. Fukai T, Ushio-Fukai M. Superoxide dismutases: role in redox signaling, vascular function, and diseases. Antioxid. Redox Signal. 15:1583–1606.
    doi: 10.1089/ars.2011.3999pmc: PMC3151424pubmed: 21473702google scholar: lookup
  11. Garvican ER, Vaughan-Thomas A, Innes JF, Clegg PD. Biomarkers of cartilage turnover. Part 1: markers of collagen degradation and synthesis. Vet. J. 185:36–42.
    doi: 10.1002/9781118269312pubmed: 20488735google scholar: lookup
  12. Genther-Schroeder ON, Branine ME, Hansen SL. The effects of increasing supplementation of zinc-amino acid complex on growth performance, carcass characteristics, and inflammatory response of beef cattle fed ractopamine hydrochloride. J. Anim. Sci. 94:3389–3398.
    doi: 10.2527/jas.2015-0209pubmed: 27695784google scholar: lookup
  13. Genther-Schroeder ON, Branine ME, Hansen SL. The influence of supplemental Zn-amino acid complex and ractopamine hydrochloride feeding duration on growth performance and carcass characteristics of finishing beef cattle. J. Anim. Sci. .
    doi: 10.2527/jas.2015-0159pubmed: 27898862google scholar: lookup
  14. Henrotin YE, Bruckner P, Pujol JP. The role of reactive oxygen species in homeostasis and degradation of cartilage. Osteoarthr. Cartilage 11:747–755.
    doi: 10.1016/s1063-4584(03)00150-xpubmed: 13129694google scholar: lookup
  15. Hostetler CE, Kincaid RL, Mirando MA. The role of essential trace elements in embryonic and fetal development in livestock. Vet. J. 166:125–139.
    doi: 10.1016/s1090-0233(02)00310-6pubmed: 12902178google scholar: lookup
  16. Hunt CL, Leatherwood JL, Coverdale JA, Sigler DL, Vogelsang MM, Arnold CE. Effects of repeated arthrocentesis on systemic cytokine expression and leukocyte population in young horses challenged with intra-articular lipopolysaccharide. J. Anim. Sci. 97:184–191.
    doi: 10.1093/jas/sky423pmc: PMC6313106pubmed: 30423145google scholar: lookup
  17. Kahn MK, Coverdale JA, Leatherwood JL, Arnold CE, Dabareiner RA, Bradbery AN, Millican AA, Welsh TH. Age-related effects on markers of inflammation and cartilage metabolism in response to an intra-articular lipopolysaccharide challenge in horses. J. Anim. Sci. 95:671–680.
    doi: 10.2527/jas.2016.1078pubmed: 28380609google scholar: lookup
  18. Leach RM Jr. Role of manganese in mucopolysaccharide metabolism. Fed. Proc. 30:991–994.
    pubmed: 4252533
  19. Leatherwood JL, Gehl KL, Coverdale JA, Arnold CE, Dabareiner RA, Walter KN, Lamprecht ED. Influence of oral glucosamine supplementation in young horses challenged with intra-articular lipopolysaccharide. J. Anim. Sci. 94:3294–3302.
    doi: 10.2527/jas.2016-0343pubmed: 27695773google scholar: lookup
  20. Littell RC, Henry PR, Ammerman CB. Statistical analysis of repeated measures data using SAS procedures. J. Anim. Sci. 76:1216–1231.
    doi: 10.2527/1998.7641216xpubmed: 9581947google scholar: lookup
  21. Lucia JL, Coverdale JA, Arnold CE, Winsco KN. Influence of an intra-articular lipopolysaccharide challenge on markers of inflammation and cartilage metabolism in young horses. J. Anim. Sci. 91:2693–2699.
    doi: 10.2527/jas.2012-5981pubmed: 23508023google scholar: lookup
  22. Matyas JR, Atley L, Ionescu M, Eyre DR, Poole AR. Analysis of cartilage biomarkers in the early phases of canine experimental osteoarthritis. Arthritis Rheum. 50:543–552.
    doi: 10.1002/art.20027pubmed: 14872497google scholar: lookup
  23. McIlwraith C. W., and Trotter G. W.. 1996. Joint disease in the horse. Philadelphia, PA: : W.B. Saunders.
  24. Milner JM, Rowan AD, Cawston TE, Young DA. Metalloproteinase and inhibitor expression profiling of resorbing cartilage reveals pro-collagenase activation as a critical step for collagenolysis. Arthritis Res. Ther. 8:R142.
    doi: 10.1186/ar2034pmc: PMC1779431pubmed: 16919164google scholar: lookup
  25. Mueller MB, Tuan RS. Anabolic/catabolic balance in pathogenesis of osteoarthritis: identifying molecular targets. Pm R 3(6 Suppl 1):S3–S11.
    doi: 10.1016/j.pmrj.2011.05.009pubmed: 21703577google scholar: lookup
  26. NRC 2007. Nutrient requirements of horses. 6th rev. ed. Natl. Acad. Press, Washington, DC.
  27. Osorio JS, Wallace RL, Tomlinson DJ, Earleywine TJ, Socha MT, Drackley JK. Effects of source of trace minerals and plane of nutrition on growth and health of transported neonatal dairy calves. J. Dairy Sci. 95:5831–5844.
    doi: 10.3168/jds.2011-5042pubmed: 22884337google scholar: lookup
  28. Ott EA, Johnson EL. Effect of trace mineral proteinates on growth and skeletal and hoof development in yearling horses. J. Eq. Vet. Sci. 21:287–292.
  29. Palmer JL, Bertone AL. Joint structure, biochemistry and biochemical disequilibrium in synovitis and equine joint disease. Equine Vet. J. 26:263–277.
  30. Perkins TL, Green RD, Hamlin KE. Evaluation of ultrasonic estimates of carcass fat thickness and longissimus muscle area in beef cattle. J. Anim. Sci. 70:1002–1010.
    doi: 10.2527/1992.7041002xpubmed: 1582927google scholar: lookup
  31. Regan E, Flannelly J, Bowler R, Tran K, Nicks M, Carbone BD, Glueck D, Heijnen H, Mason R, Crapo J. Extracellular superoxide dismutase and oxidant damage in osteoarthritis. Arthritis Rheum. 52:3479–3491.
    doi: 10.1002/art.21387pmc: PMC2755499pubmed: 16255039google scholar: lookup
  32. Richards JD, Zhao JM, Harrell RJ, Atwell CA, Dibner JJ. Trace mineral nutrition in poultry and swine. Asian-Australas. J. Anim. Sci. 23:1527–1534.
    doi: 10.5713/ajas.2010.r.07google scholar: lookup
  33. Te Moller NCR, van Weeren PR. How exercise influences equine joint homeostasis. Vet. J. 222:60–67.
    doi: 10.1016/j.tvjl.2017.03.004pubmed: 28392152google scholar: lookup
  34. Wahlen R, Evans L, Turner J, Hearn R. The use of collision/reaction cell ICP-MS for the determination of elements in blood and serum samples. Spectroscopy 20:84–89.
    doi: 10.1039/B312250Fgoogle scholar: lookup
  35. Westervelt RG, Stouffer JR, Hintz HF, Schryver HF. Estimating fatness in horses and ponies. J. Anim. Sci. 43:781–785.
    doi: 10.2527/jas1976.434781xgoogle scholar: lookup
  36. Yazar M, Sarban S, Kocyigit A, Isikan UE. Synovial fluid and plasma selenium, copper, zinc, and iron concentrations in patients with rheumatoid arthritis and osteoarthritis. Biol. Trace Elem. Res. 106:123–132.
    doi: 10.1385/BTER:106:2:123pubmed: 16116244google scholar: lookup