The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Chemical energetics of slow- and fast-twitch muscles of the mouse.
Open accessAbstract
The energy utilization associated with contraction was measured in isolated slow- and fast-twitch muscles of the mouse at 20 degrees C. The extent of this utilization was estimated from either the extent of high-energy phosphate splitting occurring during contraction (the initial chemical change, delta approximately P init) or from the extent of recovery resynthesis calculated from the observed oxygen consumption and lactate production occurring during the recovery period (recovery chemical resynthesis, delta approximately P rec). For short tetani, the cost to maintain isometric tension in the fast-twitch extensor digitorum longus (EDL) was approximately threefold greater than that in the slow-twitch soleus. With prolonged stimulation, however, the energy cost in the EDL diminished so that after 12 s of stimulation, the energy cost in the EDL was only 50% greater than that of the soleus. For both the slow-twitch soleus and the fast-twitch EDL and for all tetanus durations (up to 15 s), the extent of the initial chemical change was identical with the amount of recovery chemical resynthesis, showing that a biochemical energy balance existed in these muscles.
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Cites
Goodman, M. N., & Lowenstein, J. M. (1977) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)40157-8 · Cited by 155 · cited 2×
“During contraction, the extent of release of lactate as well as other possible termination products of the glycolytic sequence (pyruvate, alanine, glutamine, and ammonia) was similar in amount to that reported for rat muscles (Goodman and Lowenstein, 1977).”
BackgroundResultAMP deamination and IMP reamination in working skeletal muscle
Meyer, R. A., & Terjung, R. L. (1980) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1980.239.1.c32 · Cited by 143
Cited by
Fiber Types in Mammalian Skeletal Muscles
Schiaffino, S., & Reggiani, C. (2011) · Physiological Reviews · doi:10.1152/physrev.00031.2010 · Cited by 3,022
Neuronal Stimulation Triggers Neuronal Glycolysis and Not Lactate Uptake
Díaz-García, C. M., Mongeon, R., Lahmann, C., Koveal, D., Zucker, H., & Yellen, G. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.06.021 · Cited by 466
“However, it is known that in the evolution of skeletal muscle, themuscle fibers with themost dynamic energy requirements (the fast-twitch fibers) tend to rely on glycolysis for prompt energy production (Crow and Kushmerick, 1982; Spriet, 1989).”
Influence of muscle fiber type and pedal frequency on oxygen uptake kinetics of heavy exercise
Barstow, T. J., Jones, A. M., Nguyen, P. H., & Casaburi, R. (1996) · Journal of Applied Physiology · doi:10.1152/jappl.1996.81.4.1642 · Cited by 448
Motor unit recruitment during neuromuscular electrical stimulation: a critical appraisal
Bickel, C. S., Gregory, C. M., & Dean, J. C. (2011) · European Journal of Applied Physiology · doi:10.1007/s00421-011-2128-4 · Cited by 391
Fueling thought: Management of glycolysis and oxidative phosphorylation in neuronal metabolism
Yellen, G. (2018) · Journal of Cell Biology · doi:10.1083/jcb.201803152 · Cited by 371
“If the stimulated brain uses glycolysis as a low-capacity but fast mechanism for ATP production (as argued for fast-twitch skeletal muscle, for instance; Crow and Kushmerick, 1982; Spriet, 1989), it would make sense teleologically for this fast ATP resupply to occur within neurons, where the acute demand for energy is…”
BackgroundMethod
Metadata
- Authors
- Crow, M. T., & Kushmerick, M. J.
- Venue
- The Journal of general physiology
- Publisher
- Rockefeller University Press
- Published
- 1982-01-01
- Volume
- 79
- Issue
- 1
- Pages
- 147-166
- ISSN
- 0022-1295 (ISSN-L)
- 1540-7748
- OpenAlex
- W2130999848
- Cited by
- 549
- References
- 2
- FWCI
- 4.42
- Type
- journal article
- Language
- en
- Open access
- bronze
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