2000
DOI: 10.1267/ahc.33.295
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Cell Size and Succinate Dehydrogenase Activity of Different Types of Fibers in Different Regions of the Tibialis Anterior Muscle in Mice and Rats.

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Cited by 25 publications
(34 citation statements)
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“…The metabolic properties of muscle fibers also differ among fiber types [12,30,31]. The oxidative enzyme activity is higher in type IIA fibers than in type I fibers of the rat slow skeletal muscle, while the oxidative enzyme activity is higher in type I and type IIA fibers than in type IIB fibers of the rat fast skeletal muscle.…”
Section: Discussionmentioning
confidence: 97%
See 1 more Smart Citation
“…The metabolic properties of muscle fibers also differ among fiber types [12,30,31]. The oxidative enzyme activity is higher in type IIA fibers than in type I fibers of the rat slow skeletal muscle, while the oxidative enzyme activity is higher in type I and type IIA fibers than in type IIB fibers of the rat fast skeletal muscle.…”
Section: Discussionmentioning
confidence: 97%
“…The fiber type distribution of the soleus muscle was determined from the entire transverse section of the muscle, while that of the plantaris muscle was determined from~500 fibers in the middle region of the transverse section of the muscle. The cross-sectional area of each fiber was measured using a computer-assisted image processing system (Neuroimaging System) on the ATPase-stained (pH 10.4) sections [12,30,31].…”
Section: Fiber Type Classificationmentioning
confidence: 99%
“…Skeletal muscle fibers generally consist of type 1 (slow twitch, oxidative), type 2A (fast twitch, oxidative, glycolytic) and type 2B (fast twitch, glycolytic) fibers, which can be identified by ATPase staining [4]. These fibers demonstrate physiologic properties unique to each type, and these properties have been shown to be closely related to muscle function [12]. Different types of myosin isoforms, e.g., alpha-cardiac and neonatal isoforms, have also been described in the masseter [5,30,35].…”
Section: Discussionmentioning
confidence: 99%
“…The sections were incubated for the demonstration of ATPase and SDH [12,13,23,24]. For determination of the alkali preincubation ATPase activity, the following procedures were employed: 1) preincubation for 15 min at room temperature in 75 mM glycine, 50 mM CaCl2, and 75 mM NaCl in distilled water, adjusted to pH 10.4 with NaOH; 2) washing in 5 changes of distilled water; 3) incubation for 45 min at 37°C in 2.8 mM ATP, 50 mM CaCl 2 , and 75 mM NaCl in distilled water, adjusted to pH 9.4 with NaOH; 4) washing in 5 changes of distilled water; 5) immersion for 3 min in 1% CaCl2; 6) washing in 5 changes of distilled water; 7) immersion for 3 min in 2% CoCl2; 8) washing in 5 changes of distilled water; 9) immersion for 1 min in 1% (NH 4 ) 2 S; 10) washing in 5 changes of distilled water; and 11) dehydration in a graded series of ethanol, passing through xylene and then coverslipping.…”
Section: Tissue Preparationmentioning
confidence: 99%