Effects of inhibitors on contractions of normal and dystrophic mouse muscles

Author:

Brust Manfred1

Affiliation:

1. Division of Physiology, Institute for Muscle Disease, Inc., New York City

Abstract

Exposure to 0.05 mm 2,4-dinitrophenol (DNP), 1 mm NaN3, and 1 mm KCN reveals the following differences between normal and dystrophic excised, curarized gastrocnemius muscles of mice of strain 129. DNP briefly enhances twitch but not tetanus tension in rested dystrophic mice before depressing both tensions. In rested normal mice these tensions decline immediately. NaN3 reduces tensions in rested normal mice for 30 min; slow recovery follows. Half-relaxation rate is also reduced. In rested dystrophic mice tension does not recover from depression in NaN3, and the relaxation rate increases. During fatigue, tension output in dystrophic declines less rapidly than in normal mice, regardless of inhibitors. NaN3 accentuates fatigue-associated increases of contraction rate in dystrophic mice, but accelerates the usual reduction of this rate in normal ones. The two muscle groups also show quantitative differences in their responses to the inhibitors. Except for some DNP effects, all changes are reversible. Known actions of the inhibitors account only inadequately for these observations, and no clearly identifiable metabolic lesions of dystrophic muscles emerge.

Publisher

American Physiological Society

Subject

Physiology (medical)

Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Active state of normal and dystrophic mouse muscle;American Journal of Physiology-Legacy Content;1976-04-01

2. Fatigue and caffeine effects in fast-twitch and slow-twitch muscles of the mouse;Pfl�gers Archiv European Journal of Physiology;1976

3. Effect of serum on fatigue of normal and dystrophic muscles;American Journal of Physiology-Legacy Content;1970-05-01

4. Effects of series of tetani on dystrophic and normal muscles of mouse;American Journal of Physiology-Legacy Content;1966-10-01

5. Changes in contractility of frog muscle due to fatigue and inhibitors;American Journal of Physiology-Legacy Content;1964-05-01

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