Abstract
We examined reactive oxygen species as upstream activators of nuclear factor kappaB; (NF-kappaB) and forkhead box O (Foxo) in skeletal muscle during disuse atrophy. Catalase, an enzyme that degrades H2O2, was overexpressed in soleus muscles via plasmid injection prior to 7 days of hindlimb immobilization. The increased catalase activity abolished immobilization-induced transactivation of both NF-kappaB and Foxo and attenuated the loss of muscle mass. Thus, H2O2 may be an important initiator of these signaling pathways that lead to muscle atrophy.
Publication types
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Comparative Study
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Research Support, N.I.H., Extramural
MeSH terms
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Animals
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Blotting, Western
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Cell Line
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Disease Models, Animal
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Enzyme Activation / physiology*
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Follow-Up Studies
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Forkhead Transcription Factors / drug effects
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Forkhead Transcription Factors / metabolism*
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Male
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Muscle, Skeletal / metabolism*
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Muscle, Skeletal / pathology
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Muscular Disorders, Atrophic / metabolism*
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Muscular Disorders, Atrophic / pathology
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NF-kappa B / drug effects
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NF-kappa B / metabolism*
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Rats
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Rats, Sprague-Dawley
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Reactive Oxygen Species / pharmacology*
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Signal Transduction
Substances
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Forkhead Transcription Factors
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NF-kappa B
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Reactive Oxygen Species