Millisecond-scale biochemical response to change in strain.

Muscle fiber contraction involves the cyclical interaction of myosin cross-bridges with actin filaments, linked to hydrolysis of ATP that provides the required energy. We show here the relationship between cross-bridge states, force generation, and Pi release during ramp stretches of active mammalian skeletal muscle fibers at 20°C. The results show that force and Pi release respond quickly to the application of stretch: force rises rapidly, whereas the rate of Pi release decreases abruptly and remains low for the duration of the stretch. These measurements show that biochemical change on the millisecond timescale accompanies the mechanical and structural responses in active muscle fibers. A cross-bridge model is used to simulate the effect of stretch on the distribution of actomyosin cross-bridges, force, and Pi release, with explicit inclusion of ATP, ADP, and Pi in the biochemical states and length-dependence of transitions. In the simulation, stretch causes rapid detachment and reattachment of cross-bridges without release of Pi or ATP hydrolysis.

The effects of short-term sprint training on MCT expression in moderately endurance-trained runners.

The purpose of this study was to assess the effects of short-term sprint training on transient changes in monocarboxylate lactate transporter 1 (MCT1) and MCT4 protein and mRNA content. Seven moderately endurance-trained runners (mean +/- SE; age 27.7+/-2.9 years, body mass 81.1+/-5.9 kg, .VO(2max) 58.1+/-2.0 ml kg(-1) min(-1)) completed a .VO(2max) and a supramaximal running test to exhaustion (RTE) before and after a 6-week period of sprint training. The sprint training was progressive and consisted of 18 sessions of near maximal short duration (5-15 s) sprints to compliment the athlete's endurance training. Prior to the training period there was a significant (P<0.05) increase in MCT1, but not MCT4 protein, 2 h after the RTE. This occurred without any change in corresponding mRNA levels. After the training period, there was a significant increase in MCT1 protein but no significant change in the MCT4 isoform. Both MCT1 and MCT4 mRNA was significantly lower at rest and 2 h post-RTE after the completion of the training period. After the training period, there was a significant increase in the time to exhaustion and distance covered during the RTE. This study demonstrates that sprint training of this length and type results in an upregulation of MCT1 protein, but not MCT4 content. Additionally, this study shows conflicting adaptations in MCT1 and MCT4 protein and mRNA levels following training, which may indicate post-transcriptional regulation of MCT expression in human muscle.

.VO2 is attenuated above the lactate threshold in endurance-trained runners.

PURPOSE: To determine whether a deviation from linearity occurs in the .VO2-speed relationship, above the lactate threshold (LT) in running; and whether the length of the submaximal exercise bouts alters the magnitude of any deviation. METHODS: Ten endurance-trained runners (N = 3 state level, N = 4 club level, and N = 3 recreational) (mean +/- SE; age 24.4 +/- 2.8 yr, mass 76.1 +/- 2.2 kg, .VO2 59.3 +/- 10.6 mL.kg-1.min-1) completed a .VO2, LT test and 10 x 4-min submaximal constant load exercise bouts. Data were evenly spread above and below LT, which was fitted by a dual linear regression model. RESULTS: There was a significant decrease (51.4%) in slope of the .VO2-speed relationship above LT. The use of 3-min, in comparison with 4-min, submaximal data did not alter the slope of the .VO2-speed regression above LT. There was no significant difference in the .VO2max estimated from the .VO2-speed regression above LT (58.1 +/- 3.3 mL.kg-1.min-1) but a significant difference below LT (63.6 +/- 3.9 mL.kg-1.min-1) to that obtained during the .VO2max test. CONCLUSION: Data from the current study suggest that the use of the linear regression of .VO2-speed data below the LT may potentially overestimate the prediction of .VO2 values above LT.