Key result
Dystrophic mouse muscle matches normal fatigue patterns but exhibits weaker contractions and longer twitch times.
Dystrophic mouse muscles do not exhibit unique resistance to fatigue in vitro compared to normal muscles, but demonstrate weaker contraction and longer twitch times.
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Animal data on dystrophic muscle should not guide clinical fatigue assessment; leaves open in vivo and human translation.
A study of muscles of the dystrophic mouse has failed to substantiate earlier claims that these muscles were especially resistant to fatigue in vitro or that fast muscles are preferentially damaged. It has been found that the fast muscle selected for previous studies is very often unable to withstand isolation in an organ bath if it is working, and both the difficulty in removing the normal gastrocnemius muscle intact and the need to trim it surgically contribute independently toward its deterioration in vitro. The smaller dystrophic gastrocnemius muscle is less liable to excision damage, is able to satisfy its resting metabolic needs in nutrient solution, and requires no damaging dissection, but is nevertheless unable to recover normally from fatigue. Using EDL and soleus muscles which are small enough to withstand isolation in vitro, no differences are found between fatigue patterns of normal and dystrophic specimens. Responses to rest, KCl, and 2 mM caffeine are also quite similar, and the only distinguishing biomechanical characteristic we have found in dystrophic mouse muscle is a weaker contraction and a longer total twitch time.
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Hofmann et al. (1973) studied Muscular dystrophy (dystrophic mouse muscle). Dystrophic mouse muscle vs. Normal mouse muscle was evaluated on Fatigue patterns and biomechanical characteristics. Dystrophic mouse muscle showed no differences in fatigue patterns compared to normal specimens in vitro, with the only distinguishing biomechanical characteristic being a weaker contraction and longer total twitch time.
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