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A Lactate Kinetics Method for Assessing the Maximal Lactate Steady State Workload

During a continuously increasing exercise workload (WL) a point will be reached at which arterial lactate accumulates rapidly. This so-called lactate threshold (LT) is associated with the maximal lactate steady state workload (MLSS(W)), the highest WL, at which arterial lactate concentration [LA] do...

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Detalles Bibliográficos
Autores principales: Hering, Gernot O., Hennig, Ewald M., Riehle, Hartmut J., Stepan, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5884876/
https://www.ncbi.nlm.nih.gov/pubmed/29651253
http://dx.doi.org/10.3389/fphys.2018.00310
Descripción
Sumario:During a continuously increasing exercise workload (WL) a point will be reached at which arterial lactate accumulates rapidly. This so-called lactate threshold (LT) is associated with the maximal lactate steady state workload (MLSS(W)), the highest WL, at which arterial lactate concentration [LA] does not change. However, the physiological range in which the LT and the MLSS(W) occur has not been demonstrated directly. We used minor WL variations in the MLSS(W) range to assess arterial lactate kinetics in 278 treadmill and 148 bicycle ergometer exercise tests. At a certain workload, minimal further increment of running speed (0.1–0.15 m/s) or cycling power (7–10 W) caused a steep elevation of [LA] (0.9 ± 0.43 mM, maximum increase 2.4 mM), indicating LT achievement. This sharp [LA] increase was more pronounced when higher WL increments were used (0.1 vs. 0.30 m/s, P = 0.02; 0.15 vs. 0.30 m/s, P < 0.001; 7 vs. 15 W, P = 0.002; 10 vs. 15 W, P = 0.001). A subsequent workload reduction (0.1 m/s/7 W) stopped the [LA] increase indicating MLSS(W) realization. LT based determination of running speed (MLSS(W)) was highly reproducible on a day-to-day basis (r = 0.996, P < 0.001), valid in a 10 km constant velocity setting (r = 0.981, P < 0.001) and a half marathon race (r = 0.969, P < 0.001). These results demonstrate a fine-tuned regulation of exercise-related lactate metabolism, which can be reliably captured by assessing lactate kinetics at the MLSS(W).