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CaMKII activity is reduced in skeletal muscle during sepsis

Exercise‐induced muscle hypertrophy is associated with increased calcium/calmodulin‐dependent protein kinase II (CaMKII) expression and activity. In contrast, the influence of muscle atrophy‐related conditions on CaMKII is poorly understood. Here, we tested the hypothesis that sepsis‐induced muscle...

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Published in:Journal of cellular biochemistry 2013-06, Vol.114 (6), p.1294-1305
Main Authors: Aversa, Zaira, Alamdari, Nima, Castillero, Estibaliz, Muscaritoli, Maurizio, Fanelli, Filippo Rossi, Hasselgren, Per-Olof
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container_title Journal of cellular biochemistry
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Alamdari, Nima
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Fanelli, Filippo Rossi
Hasselgren, Per-Olof
description Exercise‐induced muscle hypertrophy is associated with increased calcium/calmodulin‐dependent protein kinase II (CaMKII) expression and activity. In contrast, the influence of muscle atrophy‐related conditions on CaMKII is poorly understood. Here, we tested the hypothesis that sepsis‐induced muscle wasting is associated with reduced CaMKII expression and activity. Sepsis, induced by cecal ligation and puncture in rats, and treatment of rats with TNFα, resulted in reduced total CaMKII activity in skeletal muscle whereas autonomous CaMKII activity was unaffected. The expression of CaMKIIδ, but not β and γ, was reduced in septic muscle. In additional experiments, treatment of cultured myotubes with TNFα resulted in reduced total CaMKII activity and decreased levels of phosphorylated glycogen synthase kinase (GSK)‐3β, a downstream target of CaMKII. The present results suggest that sepsis‐induced muscle wasting is associated with reduced CaMKII activity and that TNFα may be involved in the regulation of CaMKII activity in skeletal muscle. Decreased phosphorylation (consistent with activation) of GSK‐3β may be a consequence of reduced CaMKII activity, indicating that inhibited CaMKII activity may be involved in the catabolic response to sepsis. J. Cell. Biochem. 114: 1294–1305, 2013. © 2012 Wiley Periodicals, Inc.
doi_str_mv 10.1002/jcb.24469
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In contrast, the influence of muscle atrophy‐related conditions on CaMKII is poorly understood. Here, we tested the hypothesis that sepsis‐induced muscle wasting is associated with reduced CaMKII expression and activity. Sepsis, induced by cecal ligation and puncture in rats, and treatment of rats with TNFα, resulted in reduced total CaMKII activity in skeletal muscle whereas autonomous CaMKII activity was unaffected. The expression of CaMKIIδ, but not β and γ, was reduced in septic muscle. In additional experiments, treatment of cultured myotubes with TNFα resulted in reduced total CaMKII activity and decreased levels of phosphorylated glycogen synthase kinase (GSK)‐3β, a downstream target of CaMKII. The present results suggest that sepsis‐induced muscle wasting is associated with reduced CaMKII activity and that TNFα may be involved in the regulation of CaMKII activity in skeletal muscle. 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subjects Animals
ATROGIN-1
Calcium-Calmodulin-Dependent Protein Kinase Type 2 - genetics
Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism
CaMKII
Cell Line
Gene Expression
Glycogen Synthase Kinase 3 - metabolism
Glycogen Synthase Kinase 3 beta
GSK-3β
Male
MuRF1
Muscle Fibers, Fast-Twitch - enzymology
Muscle Fibers, Fast-Twitch - microbiology
Muscle Fibers, Fast-Twitch - pathology
MUSCLE WASTING
Muscle, Skeletal - enzymology
Muscle, Skeletal - microbiology
Muscle, Skeletal - pathology
Peritonitis - enzymology
Peritonitis - microbiology
Phosphorylation
Protein Processing, Post-Translational
Rats
Rats, Sprague-Dawley
RNA, Messenger - genetics
RNA, Messenger - metabolism
SEPSIS
Sepsis - enzymology
Serum Response Factor - metabolism
title CaMKII activity is reduced in skeletal muscle during sepsis
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