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pubmed-article:8048492pubmed:abstractTextSelected enzymes were measured in mixed-fiber bundles and individual fibers from rat plantaris (PL) and soleus (Sol) muscles that had undergone either 2 wk of tetrodotoxin (TTX) inactivation of the sciatic nerve, a sham operation, or were contralateral to the TTX limb. TTX disuse caused severe wasting of PL (46%) and Sol (26%) muscles and of single fibers (50% and 40%, respectively). TTX PL and Sol also had reduced (50%) glycogen content. In TTX, PL, and Sol macro samples and single fibers, the activities (mol.h-1.kg dry wt-1) of hexokinase, glycogen phosphorylase, and lactate dehydrogenase were higher, lower, and unchanged, respectively, compared with controls. Single-fiber data showed that these changes occurred in all fibers. In TTX PL macro samples, activities of glycerol-3-phosphate dehydrogenase (GPDH), pyruvate kinase (PK), malate dehydrogenase (MDH), citrate synthase (CS), beta-hydroxyacyl-CoA dehydrogenase (BOAC), and thiolase were, or tended to be, lower. Single-fiber data showed a disappearance of high-oxidative moderate glycolytic fibers (i.e., usually fast-twitch oxidative in control) and the appearance of more fibers with a metabolic enzyme profile approaching that of control slow-oxidative fibers. In TTX Sol macro samples, GPDH and PK tended to be higher, and thiolase, BOAC, CS, and MDH lower. Single-fiber data corroborated these findings and suggested the appearance of fast fibers with downregulated oxidative enzyme profiles. Our results suggest that neuromuscular activity is a major, but not the sole, determinant of the size and metabolic heterogeneity that exists in muscle cells.lld:pubmed
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pubmed-article:8048492pubmed:authorpubmed-author:LowryO HOHlld:pubmed
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pubmed-article:8048492pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:8048492pubmed:articleTitleEffects of tetrodotoxin-induced neural inactivation on single muscle fiber metabolic enzymes.lld:pubmed
pubmed-article:8048492pubmed:affiliationSchool of Human Movement, Laurentian University, Sudbury, Ontario, Canada.lld:pubmed
pubmed-article:8048492pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8048492pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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