2 results
Evaluation of oxygen consumption during field exercise tests in Standardbred trotters
- Emmanuelle van Erck, Dominique-Marie Votion, Didier Serteyn, Tatiana Art
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- Journal:
- Equine and Comparative Exercise Physiology / Volume 4 / Issue 1 / February 2007
- Published online by Cambridge University Press:
- 01 February 2007, pp. 43-49
- Print publication:
- February 2007
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Reasons for performing the study: In human exercise physiology, the current gold standard for evaluating aerobic capacity is the measurement of oxygen consumption (VO2) and maximal oxygen uptake (VO2max). The evaluation of VO2 in horses is performed in some laboratories equipped with a treadmill but has only been exceptionally reported in field conditions because of the lack of adapted equipment. Objectives: The aim of this study was (1) to assess the feasibility of VO2 measurement on the track using a recently validated portable breath-by-breath gas analyser system adapted to horses (Cosmed K4b2® and Equimask®), (2) to compare these results with those obtained during a treadmill exercise test and (3) to study correlations between VO2 and physiological parameters usually measured in field condition such as heart rate (HR), lactataemia (LA) and the speed at which HR equals 200 beats per minute (bpm) (V200) or LA 4 mmol l− 1 (VLA4). Methods: Five healthy Standardbred trotters in training were submitted to two stepwise incremental exercise tests, one driven on the racetrack and the other on a high-speed treadmill with a 4% incline. Speed (v), HR, ventilatory parameters and VO2 were continuously recorded throughout the duration of the tests and LA was evaluated after each step. Results: All horses completed the test satisfactorily after an initial acclimatization to the mask. There were marked individual differences in ventilatory strategy, and breathing frequency (Rf) at the higher levels of exercise was noticeably low. The VCO2 measurements were incoherent. There were no significant differences between track and treadmill maximal data obtained during the last step [VO2peak (track: 139.9 ± 8.9 ml kg− 1 min− 1; treadmill: 139.9 ± 13.4 ml kg− 1 min− 1), LAmax (track: 6.5 ± 1.6 mmol l− 1; treadmill: 7.3 ± 3.0 mmol l− 1), HRmax (track: 229 ± 6.2 bpm; treadmill: 222 ± 13 bpm)], although the maximal speed required to reach similar workloads was significantly higher on the track (11.9 ± 0.6 m s− 1vs. 9.7 ± 0.4 m s− 1). The correlation between VO2 and HR (r = 0.87; P < 0.001) and VO2 and LA (r = 0.75; P < 0.0001) during both tests was good but no correlation was found between VO2peak and HRmax, LAmax, V200 or VLA4. Conclusions: This is the first report of a practical portable system to measure VO2 and ventilation continuously during high-speed field exercise tests. However, current mask design markedly influences ventilation and could have prohibited the attainment of VO2max. Furthermore, consistent VCO2 measurements should be implemented by the manufacturers. Potential relevance: Continuous breath-by-breath ventilation and VO2 measurements can be recorded in horses in the field at submaximal levels. With necessary adaptations to the system entailed, this study opens new perspectives in the analysis of physiological and metabolic mechanisms of exercise in the equine species in genuine track conditions.
Assessment of the oxidant–antioxidant blood balance in a field exercise test in Standardbredand eventing horses
- Brieuc de Moffarts, Nathalie Kirschvink, Emmanuelle van Erck, Tatiana Art, Joël Pincemail, Pierre Lekeux
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- Journal:
- Equine and Comparative Exercise Physiology / Volume 2 / Issue 4 / November 2005
- Published online by Cambridge University Press:
- 09 March 2007, pp. 253-261
- Print publication:
- November 2005
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The aim of this study was to determine which oxidant–antioxidant blood markers are of interest for a field exercise test (ET) performed on a racetrack. Healthy Standardbred horses (S: n = 12) and healthy eventing horses (E: n=12) were investigated. Exercise was monitored by measuring velocity (V), heart rate (HR), and plasma lactate (LA). Whilst maximal LA did not differ (11.8±0.88 mmol l−1), maximal V (S: 12.3±0.17 m s−1versus E: 11.1±0.24 m s−1, P<0.05) and final HR (S: 222±1 versus E: 203±8 beats min−1, P<0.05) were significantly different between groups. Venous blood was collected at rest (R) prior to ET and the following oxidant–antioxidant markers were determined: uric acid (UA), ascorbic acid (AA), α-tocopherol (Vit E), vitamin A (Vit A), superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione (reduced: GSH and oxidized: GSSG), glutathione redox ratio (GRR), copper (Cu), zinc (Zn) and selenium (Se), oxidized proteins (Protox), lipid peroxides (Pool), antioxidant capacity of water-soluble components (ACW) and antioxidant capacity of lipid-soluble components (ACL). The following markers were further determined 15 min (E15) after the ET: UA, ACW, AA, GSH, Protox, Pool, ACL. Standardbreds had significantly higher concentrations of ACW, GSH, ACL and Protox, whilst Se, Zn and SOD were significantly lower than in eventing horses. Exercise induced a significant increase in ACW and UA. GSH decreased in eventing horses and Pool significantly decreased in both horse groups. This study describes a field ET of high intensity for Standardbred and eventing horses, which could be performed by all animals tested. By sampling blood at rest and at E15, changes of the hydrophilic antioxidant defence were partially assessed, whereas no interpretable changes of the lipophilic antioxidants and of oxidation markers (Protox, Pool) could be detected.