Billat Veronique L, Mouisel Etienne, Roblot Natacha, Melki Judith
Laboratory of Exercise Physiology, UFRSFA, Université d'Evry-Val d'Essonne Boulevard François Mitterrand, 94025 Evry Cedex France.
J Appl Physiol (1985). 2005 Apr;98(4):1258-63. doi: 10.1152/japplphysiol.00991.2004. Epub 2004 Nov 12.
With the generation of mouse models of human cardiovascular or neuromuscular disorders, the development of noninvasive methods to evaluate the physiological responses to exercise presents an important challenge. The possibility for determining critical speed (CS) in the mouse model was examined according to strain (CD1, C57BL/6J, FVB/N) and sex. Sixty mice performed four exhaustive runs on a treadmill to determine their CS. Twenty-one performed an incremental test to determine the velocity at the lactate threshold. CS was significantly different between the strains (P < 0.0001) but not between sexes. Two measures of heritability showed that CS was partially heritable. CS was not significantly different from lactate threshold velocity. We conclude that CS, which reflects the aerobic capacity, can be determined in mice, as in humans and horses. Considering the intrastrain variability, CS could represent a valuable means for designing an optimal and individualized physical training in mice.
随着人类心血管或神经肌肉疾病小鼠模型的产生,开发用于评估运动生理反应的非侵入性方法面临着一项重大挑战。根据品系(CD1、C57BL/6J、FVB/N)和性别,研究了在小鼠模型中确定临界速度(CS)的可能性。60只小鼠在跑步机上进行了4次力竭性跑步以确定其CS。21只小鼠进行了递增测试以确定乳酸阈值时的速度。品系之间的CS存在显著差异(P < 0.0001),但性别之间无显著差异。两种遗传力测量结果表明CS具有部分遗传性。CS与乳酸阈值速度无显著差异。我们得出结论,与人类和马匹一样,在小鼠中也可以确定反映有氧能力的CS。考虑到品系内的变异性,CS可能是为小鼠设计最佳个性化体育训练的一种有价值的手段。