Analyze Diet
Journal of animal physiology and animal nutrition2024; 109(1); 113-123; doi: 10.1111/jpn.14037

The effect of the fat to starch ratio in young horses’ diet on plasma metabolites, muscle endurance and fear responses.

Abstract: High-starch diets may affect equine hindgut microbiota and increase blood glucose levels, which may cause unwanted physiological changes, but may also elicit behavioural changes such as increased fear reactions. The purpose of the current study was to feed a high starch (300) and low fat (43; HS_LF) or a low starch (60) and high fat (85; LS_HF, g/kg of DM) concentrate within the available commercial range and investigate how muscle endurance and fear reactions of horses respond to different diets. Twenty Danish Warmblood stallions (4 years) were randomly allocated to two treatments: LS_HF (n = 10) and HS_LF (n = 10) for 9 weeks. During the two last weeks, a single step exercise test was performed, and plasma metabolites and blood gases were measured before and after exercise in a 2 × 2 factorial design. The effect of two diets on fearfulness was tested by exposing the horses to novel objects test (T1 and T2). Plasma metabolites was not affected by diets. However, plasma level of glucose post-exercise (4.9) was lower than pre-exercise (5.6 mmol/L; p < 0.001). Similarly, plasma level of insulin post-exercise (4.2) was lower than pre-exercise (13.1 pmol/L; p < 0.001). Plasma level of lactate dehydrogenase (p < 0.001), non-esterified fatty acids (p = 0.002), β-hydroxybutyrate (p = 0.001), and fructosamine (p = 0.01) post-exercise was higher than pre-exercise. Regardless of type of diets, RRR-α-tocopherol was the dominance α-tocopherol stereoisomers in plasma. In conclusion, during aerobic exercise, fat to starch ratio in horse diets within the normal range had no significant effect on plasma metabolites. However, horses fed LS_HF tended to show more investigative behaviour than horses fed HS_LF.
Publication Date: 2024-08-20 PubMed ID: 39163118PubMed Central: PMC11731427DOI: 10.1111/jpn.14037Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Randomized Controlled Trial
  • Veterinary

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.

This study examines how varying the fat-to-starch ratio in the diets of young horses affects their plasma metabolites, muscle endurance, and fear responses. The researchers found no significant impact on plasma metabolites, but did notice a tendency towards more investigative behaviour in horses fed a low-starch, high-fat diet.

Research Methodology

  • The research involved twenty 4-year-old Danish Warmblood stallions, split into two groups of ten. Each group was fed a different diet for nine weeks. One group consumed a high-starch, low-fat meal (HS_LF), while the other was given a low-starch, high-fat diet (LS_HF).
  • During the final two weeks of this period, the horses underwent a single step exercise test.
  • Researchers measured the horses’ plasma metabolites and blood gases before and after exercising, in a 2 × 2 factorial design.
  • The effect of the different diets on fearfulness was examined by exposing the horses to unknown objects (a novel objects test).

Research Findings

  • There was no significant impact of dietary composition on plasma metabolites.
  • Post-exercise, plasma glucose levels decreased from 5.6 mmol/L pre-exercise to 4.9 mmol/L. Similarly, plasma insulin levels after exercise were lower (4.2) than before (13.1 pmol/L), with both changes being statistically significant (p < 0.001).
  • After exercise, levels of lactate dehydrogenase, non-esterified fatty acids, β-hydroxybutyrate, and fructosamine in the plasma were higher than before. These changes were also statistically significant.
  • Regardless of the diet, RRR-α-tocopherol was the dominant α-tocopherol stereoisomer in the plasma.
  • The dietary variation did not have a noticeable impact on plasma metabolites during aerobic exercise. However, the horses consuming the LS_HF diet displayed more investigative behaviour than those fed the HS_LF diet.

Cite This Article

APA
Lashkari S, Beblein C, Christensen JW, Jensen SK. (2024). The effect of the fat to starch ratio in young horses’ diet on plasma metabolites, muscle endurance and fear responses. J Anim Physiol Anim Nutr (Berl), 109(1), 113-123. https://doi.org/10.1111/jpn.14037

Publication

ISSN: 1439-0396
NlmUniqueID: 101126979
Country: Germany
Language: English
Volume: 109
Issue: 1
Pages: 113-123

Researcher Affiliations

Lashkari, Saman
  • Department of Animal and Veterinary Sciences, Aarhus University, AU Viborg, Research Centre Foulum, Tjele, Denmark.
Beblein, Carina
  • Department of Animal and Veterinary Sciences, Aarhus University, AU Viborg, Research Centre Foulum, Tjele, Denmark.
  • Marketing Department, Pavo Horse feed, Vojens, Denmark.
Christensen, Janne W
  • Department of Animal and Veterinary Sciences, Aarhus University, AU Viborg, Research Centre Foulum, Tjele, Denmark.
Jensen, Søren K
  • Department of Animal and Veterinary Sciences, Aarhus University, AU Viborg, Research Centre Foulum, Tjele, Denmark.

MeSH Terms

  • Animals
  • Horses / physiology
  • Horses / blood
  • Starch / administration & dosage
  • Starch / pharmacology
  • Starch / chemistry
  • Animal Feed / analysis
  • Diet / veterinary
  • Animal Nutritional Physiological Phenomena
  • Male
  • Fear
  • Dietary Fats / administration & dosage
  • Dietary Fats / pharmacology
  • Muscle, Skeletal / physiology
  • Physical Conditioning, Animal
  • Physical Endurance / drug effects

Grant Funding

  • St. Hippolyt and the Toosbuy foundation
  • Aarhus Universitet

Conflict of Interest Statement

The authors declare no conflicts of interest.

References

This article includes 54 references
  1. Aguilera‐Tejero E, Estepa JC, López I, Bas S, Mayer‐Valor R, Rodríguez M. Quantitative analysis of acid–base balance in show jumpers before and after exercise. Research in Veterinary Science 68(2), 103–108.
    pubmed: 10756125
  2. Allaam M, Elseady Y, Nayel M, Elsify A, Salama A, Hassan H, Kamar A. Physiological and hemato‐chemical evaluation of thoroughbred race horse after exercise. IJAVMS 8(3), 81–93.
  3. Andrade FH, McMullen CA. Lactate is a metabolic substrate that sustains extraocular muscle function. Pflügers Archiv – European Journal of Physiology 452(1), 102–108.
    pubmed: 16328456
  4. Avellini L, Silvestrelli M, Gaiti A. Training‐induced modifications in some biochemical defences against free radicals in equine erythrocytes. Veterinary Research Communications 19(3), 179–184.
    pubmed: 7571391
  5. Balogh N, Gaál T, Ribiczeyné PS, Petri Á. Biochemical and antioxidant changes in plasma and erythrocytes of pentathlon horses before and after exercise. Veterinary Clinical Pathology 30(4), 214–218.
    pubmed: 12024305
  6. Blatt DH, Pryor WA, Mata JE, Rodriguez‐Proteau R. Re‐evaluation of the relative potency of synthetic and natural α‐tocopherol: experimental and clinical observations. The Journal of Nutritional Biochemistry 15(7), 380–395.
    pubmed: 15219923
  7. Bulmer L, McBride S, Williams K, Murray J.‐A.. The effects of a high‐starch or high‐fibre diet on equine reactivity and handling behaviour. Applied Animal Behaviour Science 165, 95–102.
  8. Bulmer LS, Murray J.‐A., Burns NM, Garber A, Wemelsfelder F, McEwan NR, Hastie PM. High‐starch diets alter equine faecal microbiota and increase behavioural reactivity. Scientific Reports 9(1), 18621.
    pmc: PMC6901590pubmed: 31819069
  9. Christensen JW, Beblein C, Malmkvist J. Development and consistency of fearfulness in horses from foal to adult. Applied Animal Behaviour Science 232, 105106.
  10. Davie AL, Evans DJ. Blood lactate responses to submaximal field exercise tests in Thoroughbred horses. The Veterinary Journal 159(3), 252–258.
    pubmed: 10775469
  11. Delobel A, Cuvelier C. Fat‐supplemented diets for horses: characteristics, palatability and digestibility. .
  12. Freire R, Clegg HA, Buckley P, Friend MA, McGreevy PD. The effects of two different amounts of dietary grain on the digestibility of the diet and behaviour of intensively managed horses. Applied Animal Behaviour Science 117(1–2), 69–73.
  13. Geor RJ, Coenen M, Harris P. Equine applied and clinical nutrition E‐book: Health, welfare and performance. .
  14. Gordon ME, McKeever KH, Betros CL, Manso Filho HC. Exercise‐induced alterations in plasma concentrations of ghrelin, adiponectin, leptin, glucose, insulin, and cortisol in horses. The Veterinary Journal 173(3), 532–540.
    pubmed: 16516509
  15. Granit R, Angel S, Akiri B, Holzer Z, Aharoni Y, Orlov A, Kanner J. Effects of vitamin E supplementation on lipid peroxidation and color retention of salted calf muscle from a diet rich in polyunsaturated fatty acids. Journal of Agricultural and Food Chemistry 49(12), 5951–5956.
    pubmed: 11743791
  16. Grimm P, Philippeau C, Julliand V. Faecal parameters as biomarkers of the equine hindgut microbial ecosystem under dietary change. Animal 11(7), 1136–1145.
    pubmed: 28065211
  17. Hall MB. Determination of starch, including maltooligosaccharides, in animal feeds: Comparison of methods and a method recommended for AOAC collaborative study. Journal of AOAC International 92(1), 42–49.
    pubmed: 19382561
  18. Hansen B. Determination of nitrogen as elementary N, an alternative to Kjeldahl. Acta Agriculturae Scandinavica 39(2), 113–118.
  19. Hansen TL, Rankins EM, Bobel JM, McKinney M, Hackmann TJ, Warren LK. Postprandial blood glucose and insulin responses of horses to feeds differing in soluble fiber concentration. Journal of equine veterinary science 88, 102963.
    pubmed: 32303311
  20. Hemmann KE, Koho NM, Vainio OM, Raekallio MR. Effects of feed on plasma leptin and ghrelin concentrations in crib‐biting horses. The Veterinary Journal 198(1), 122–126.
    pubmed: 23838207
  21. Hoffman RM. Carbohydrate metabolism and metabolic disorders in horses. Revista Brasileira de Zootecnia 38, 270–276.
  22. Hymøller L, Lashkari S, Clausen TN, Jensen SK. Distribution of α‐tocopherol stereoisomers in mink (Mustela vison) organs varies with the amount of all‐rac‐α‐tocopheryl acetate in the diet. British Journal of Nutrition 120(12), 1332–1337.
    pubmed: 30328404
  23. Jansson A, Lindberg JE. A forage‐only diet alters the metabolic response of horses in training. Animal 6(12), 1939–1946.
    pubmed: 22717208
  24. Jensen SK, Engberg RM, Hedemann MS. All‐rac‐α‐tocopherol acetate is a better vitamin E source than all‐rac‐α‐tocopherol succinate for broilers. The Journal of Nutrition 129(7), 1355–1360.
    pubmed: 10395598
  25. Jensen SK, Lashkari S, Kristensen NB. Pharmacokinetics of α‐tocopherol stereoisomers in plasma and milk of cows following a single dose injection of all‐rac‐α‐tocopheryl acetate. Food Chemistry 310, 125931.
    pubmed: 31835226
  26. Juul A, Bang P, Hertel NT, Main K, Dalgaard P, Jørgensen K, Müller J, Hall K, Skakkebaek NE. Serum insulin‐like growth factor‐I in 1030 healthy children, adolescents, and adults: Relation to age, sex, stage of puberty, testicular size, and body mass index. The Journal of Clinical Endocrinology and Metabolism 78(3), 744–752.
    pubmed: 8126152
  27. Knudsen KEB, Li BW. Determination of oligosaccharides in protein‐rich feedstuffs by gas‐liquid chromatography and high‐performance liquid chromatography. Journal of Agricultural and Food Chemistry 39(4), 689–694.
  28. Kuntz R, Kubalek C, Ruf T, Tataruch F, Arnold W. Seasonal adjustment of energy budget in a large wild mammal, the Przewalski horse (Equus ferus przewalskii) I. Energy intake. Journal of Experimental Biology 209(22), 4557–4565.
    pubmed: 17079725
  29. Lashkari S, Clausen TN, Foldager L, Jensen SK. Absorption of α‐tocopheryl acetate is limited in mink kits (Mustela vison) during weaning. Scientific Reports 11(1), 1–12.
    pmc: PMC7846754pubmed: 33514760
  30. Lashkari S, Jensen SK, Hansen CB, Krogh K, Theilgaard P, Raun BM, Vestergaard M. Feeding concentrate pellets enriched by natural vitamin E keeps the plasma vitamin E above the critical level in calves post‐weaning. Livestock Science 253, 104672.
  31. Lashkari S, Jensen SK, Vestergaard M. Response to different sources of vitamin E orally injected and to various doses of vitamin E in calf starter on the plasma vitamin E level in calves around weaning. Animal 16(4), 100492.
    pubmed: 35334395
  32. Lashkari S, Krogh Jensen S, Bernes G. Biodiscrimination of α‐tocopherol stereoisomers in plasma and tissues of lambs fed different proportions of all‐rac‐α‐tocopheryl acetate and RRR‐α‐tocopheryl acetate. Journal of Animal Science 97(3), 1222–1233.
    pmc: PMC6396261pubmed: 30624663
  33. Leonard SW, Terasawa Y, Farese Jr RV, Traber MG. Incorporation of deuterated RRR‐ or all‐rac‐α‐tocopherol in plasma and tissues of α‐tocopherol transfer protein–null mice. The American Journal of Clinical Nutrition 75(3), 555–560.
    pubmed: 11864863
  34. Lindner A, Mosen H, Kissenbeck S, Fuhrmann H, Sallmann HP. Effect of blood lactate‐guided conditioning of horses with exercises of differing durations and intensities on heart rate and biochemical blood variables. Journal of Animal Science 87(10), 3211–3217.
    pubmed: 19542497
  35. Luthersson N, Nielsen KH, Harris P, Parkin TDH. Risk factors associated with equine gastric ulceration syndrome (EGUS) in 201 horses in Denmark. Equine Veterinary Journal 41(7), 625–630.
    pubmed: 19927579
  36. Lyte M, Chapel A, Lyte JM, Ai Y, Proctor A, Jane J.‐L., Phillips GJ. Resistant starch alters the microbiota–gut brain axis: Implications for dietary modulation of behavior. PLoS One 11(1), e0146406.
    pmc: PMC4706316pubmed: 26745269
  37. Løvendahl P, Purup HM. Technical note: Time‐resolved fluoro‐immunometric assay for intact insulin in livestock species. Journal of Animal Science 80(1), 191–195.
    pubmed: 11831516
  38. Mertens DR. Gravimetric determination of amylase‐treated neutral detergent fiber in feeds with refluxing in beakers or crucibles: Collaborative study. Journal of AOAC International 85(6), 1217–1240.
    pubmed: 12477183
  39. Meyers MC, Potter GD, Evans JW, Greene LW, Crouse SF. Physiologic and metabolic response of exercising horses to added dietary fat. Journal of Equine Veterinary Science 9(4), 218–223.
  40. Mills PC, Smith NC, Casas I, Harris P, Harris RC, Marlin DJ. Effects of exercise intensity and environmental stress on indices of oxidative stress and iron homeostasis during exercise in the horse. European Journal of Applied Physiology and Occupational Physiology 74(1), 60–66.
    pubmed: 8891501
  41. Nicol CJ, Badnell‐Waters AJ, Bice R, Kelland A, Wilson AD, Harris PA. The effects of diet and weaning method on the behaviour of young horses. Applied Animal Behaviour Science 95(3–4), 205–221.
  42. Nicol CJ, Davidson HPD, Harris PA, Waters AJ, Wilson AD. Study of crib‐biting and gastric inflammation and ulceration in young horses. Veterinary Record 151(22), 658–662.
    pubmed: 12498408
  43. NRC. Nutrient requirements of horses, In: Natl (6th rev.). 2007.
  44. Redondo AJ, Carranza J, Trigo P. Fat diet reduces stress and intensity of startle reaction in horses. Applied Animal Behaviour Science 118(1–2), 69–75.
  45. Reusch CE, Liehs MR, Hoyer M, Vochezer R. Fructosamine: A new parameter for diagnosis and metabolic control in diabetic dogs and cats. Journal of Veterinary Internal Medicine 7(3), 177–182.
    pubmed: 8331612
  46. Ronéus N, Essén‐Gustavsson B, Lindholm A, Eriksson Y. Plasma lactate response to submaximal and maximal exercise tests with training, and its relationship to performance and muscle characteristics in Standardbred trotters. Equine Veterinary Journal 26(2), 117–121.
    pubmed: 8575372
  47. Ropp JK, Raub RH, Minton JE. The effect of dietary energy source on serum concentration of insulin‐like growth factor‐I, growth hormone, insulin, glucose, and fat metabolites in weanling horses. Journal of Animal Science 81(6), 1581–589.
    pubmed: 12817507
  48. Stoldt W. Vorschlag zur vereinheitlichung der fettbestimmung in lebensmitteln. Fette und Seifen 54(4), 206–207.
  49. Traber M, Burton G, Ingold K, Kayden H. RRR‐and SRR‐alpha‐tocopherols are secreted without discrimination in human chylomicrons, but RRR‐alpha‐tocopherol is preferentially secreted in very low density lipoproteins. Journal of Lipid Research 31(4), 675–685.
    pubmed: 2351872
  50. Vervuert I, Voigt K, Hollands T, Cí·¯ord D, Coenen M. Effect of feeding increasing quantities of starch on glycaemic and insulinaemic responses in healthy horses. The Veterinary Journal 182(1), 67–72.
    pubmed: 18558504
  51. Vincze A, Szabó C, Bakos Z, Szabó V, Veres S, Ü tď D, Hevesi Á. Effect of dietary energy source on the plasma parameters of equine athletes trained in a deep water aqua treadmill. Italian Journal of Animal Science 15(1), 137–143.
  52. Watson TD. Metabolic and endocrine problems of the horse. .
  53. Wernicki A, Urban‐Chmiel R, Kankofer M, Mikucki P, Puchalski A, Tokarzewski S. Evaluation of plasma cortisol and TBARS levels in calves after short‐term transportation. Revue de médecine vétérinaire 157(1), 30.
  54. Zeyner A, Bessert J, Gropp JM. Effect of feeding exercised horses on high‐starch or high‐fat diets for 390 days. Equine Veterinary Journal 34(S34), 50–57.
    pubmed: 12405659