Plasma acylcarnitine and fatty acid profiles during exercise and training in Standardbreds

Cornélie M. Westermann Department of Equine Sciences, Medicine Section, Faculty of Veterinary Medicine, Utrecht University, 3508 TD Utrecht, The Netherlands

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Bert Dorland Department of Metabolic and Endocrine Diseases, UMC Utrecht, 3508 AB Utrecht, The Netherlands

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Monique G. de Sain-van der Velden Department of Metabolic and Endocrine Diseases, UMC Utrecht, 3508 AB Utrecht, The Netherlands

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Inge D. Wijnberg Department of Equine Sciences, Medicine Section, Faculty of Veterinary Medicine, Utrecht University, 3508 TD Utrecht, The Netherlands

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Eric van Breda Department of Movement Sciences, Faculty of Health Sciences, University of Maastricht, 6200 MD Maastricht, The Netherlands

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Ellen de Graaf-Roelfsema Department of Equine Sciences, Medicine Section, Faculty of Veterinary Medicine, Utrecht University, 3508 TD Utrecht, The Netherlands

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Hans A. Keizer Department of Human Physiology and Sports Medicine, Free University of Brussels, 1050 Brussels, Belgium

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Johannes H. van der Kolk Department of Equine Sciences, Medicine Section, Faculty of Veterinary Medicine, Utrecht University, 3508 TD Utrecht, The Netherlands

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Abstract

Objective—To evaluate alterations in skeletal muscle carnitine metabolism during exercise and training by measuring changes in plasma acylcarnitine concentrations in Standardbreds.

Animals—10 Standardbred geldings with a mean ± SD age of 20 ± 2 months and weight of 384 ± 42 kg.

Procedures—In a 32-week longitudinal study, training on a treadmill was divided into 4 phases as follows: phase 1, acclimatization for 4 weeks; phase 2, 18 weeks with alternating endurance and high-intensity exercise training; phase 3, increased training volume and intensity for another 6 weeks; and phase 4, deconditioning for 4 weeks. In phase 3, horses were randomly assigned to 2 groups as follows: control horses (which continued training at the same level as in phase 2) and high-intensity exercise trained horses. At the end of each phase, a standardized exercise test (SET) was performed. Plasma acylcarnitine, fatty acids, and lactic acid and serum β-hydroxybutyric acid (BHBA) concentrations were assessed before and at different time points after each SET.

Results—Plasma lactic acid, total nonesterified fatty acids, 3-hydroxyisobutyric acid, and acetylcarnitine (C2-carnitine) concentrations significantly increased during SETs, whereas serum BHBA, plasma propionylcarnitine (C3-carnitine), and plasma butyryl- and isobutyrylcarnitine (C4-carnitine) concentrations decreased significantly, compared with those before SETs.

Conclusions and Clinical Relevance—Our findings indicated that the plasma acylcarnitine profile in horses likely reflects skeletal muscle carnitine metabolism following exercise, thereby providing a possible practical method to investigate potential disorders in carnitine metabolism in horses with myopathy.

Abstract

Objective—To evaluate alterations in skeletal muscle carnitine metabolism during exercise and training by measuring changes in plasma acylcarnitine concentrations in Standardbreds.

Animals—10 Standardbred geldings with a mean ± SD age of 20 ± 2 months and weight of 384 ± 42 kg.

Procedures—In a 32-week longitudinal study, training on a treadmill was divided into 4 phases as follows: phase 1, acclimatization for 4 weeks; phase 2, 18 weeks with alternating endurance and high-intensity exercise training; phase 3, increased training volume and intensity for another 6 weeks; and phase 4, deconditioning for 4 weeks. In phase 3, horses were randomly assigned to 2 groups as follows: control horses (which continued training at the same level as in phase 2) and high-intensity exercise trained horses. At the end of each phase, a standardized exercise test (SET) was performed. Plasma acylcarnitine, fatty acids, and lactic acid and serum β-hydroxybutyric acid (BHBA) concentrations were assessed before and at different time points after each SET.

Results—Plasma lactic acid, total nonesterified fatty acids, 3-hydroxyisobutyric acid, and acetylcarnitine (C2-carnitine) concentrations significantly increased during SETs, whereas serum BHBA, plasma propionylcarnitine (C3-carnitine), and plasma butyryl- and isobutyrylcarnitine (C4-carnitine) concentrations decreased significantly, compared with those before SETs.

Conclusions and Clinical Relevance—Our findings indicated that the plasma acylcarnitine profile in horses likely reflects skeletal muscle carnitine metabolism following exercise, thereby providing a possible practical method to investigate potential disorders in carnitine metabolism in horses with myopathy.

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