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Changes in denervated skeletal muscle of amiodarone‐fed mice

Identifieur interne : 003261 ( Main/Exploration ); précédent : 003260; suivant : 003262

Changes in denervated skeletal muscle of amiodarone‐fed mice

Auteurs : Frederic R. Costa-Jussà [Royaume-Uni] ; Ana Guevara ; Gary A. Brook [Royaume-Uni] ; Leo W. Duchen [Royaume-Uni] ; Jean M. Jacobs [Royaume-Uni]

Source :

RBID : ISTEX:84B99B180D064D739017B7A9F19382C6D66DD899

English descriptors

Abstract

Prolonged dosing of mice with amiodarone produced a myopathy characterized by autophagic vacuolation and phospholipid inclusions. A previous morphological study had shown that amiodarone did not affect the rate of nerve regeneration after sciatic nerve crush. In the present study, reinnervation was assessed by the reappearance of miniature endplate potentials that confirmed that axonal regeneration and motor reinnervation was not affected by amiodarone. However, there was a marked delay in the recovery of motor function in the amiodarone‐treated mice. Denervation was found to induce an extensive necrosis of muscle fibers in the deeper parts of fast‐twitch muscles. Histochemical studies showed that type 1 fibers were spared, necrosis affecting mainly type 2 fibers with relatively high oxidative enzyme activity (fast‐twitch oxidative fibers). Biochemical studies showed a significant increase in the amount of amiodarone and its metabolite in denervated muscle of amiodarone‐treated mice when compared with contralateral, normally innervated muscles.

Url:
DOI: 10.1002/mus.880110616


Affiliations:


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Le document en format XML

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<term>Absolute values</term>
<term>Acid phosphatase</term>
<term>Acid phosphatase activity</term>
<term>Amiodarone</term>
<term>Amiodarone toxicity</term>
<term>Autophagic vacuoles</term>
<term>Axonal regeneration</term>
<term>Biochemical studies</term>
<term>Body weight</term>
<term>Central nuclei</term>
<term>Checkerboard pattern</term>
<term>Cholinesterase activity</term>
<term>Clin pathol</term>
<term>Control animals</term>
<term>Control mice</term>
<term>Crush</term>
<term>Days dosing liver</term>
<term>Deeper parts</term>
<term>Denervated</term>
<term>Denervated muscle</term>
<term>Denervated muscles</term>
<term>Denervation</term>
<term>Dosing</term>
<term>Electron micrograph</term>
<term>Electron microscopy</term>
<term>Electrondense cores</term>
<term>Empty vacuoles</term>
<term>Endothelial cells</term>
<term>Endplate</term>
<term>Gastrocnemius muscle</term>
<term>Granular material</term>
<term>High oxidative enzyme activity</term>
<term>Higher oxidative enzyme activity</term>
<term>Histochem cytochem</term>
<term>Histochemical</term>
<term>Histochemical methods</term>
<term>Histochemical studies</term>
<term>Inclusion</term>
<term>Innervated</term>
<term>Innervated muscles</term>
<term>Intramuscular nerves</term>
<term>Jacobs</term>
<term>June</term>
<term>Lateral head</term>
<term>Lateral heads</term>
<term>Liquid chromatography</term>
<term>Many muscle fibers</term>
<term>Methyl cellulose</term>
<term>Mice muscle nerve june</term>
<term>Miniature endplate potentials</term>
<term>Motor function</term>
<term>Mouse</term>
<term>Muscle fiber regeneration</term>
<term>Muscle fibers</term>
<term>Muscle necrosis</term>
<term>Muscle nerve june</term>
<term>Muscle tensions</term>
<term>Myosin atpase</term>
<term>Necrosis</term>
<term>Necrotic fibers</term>
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<term>Nerve crush</term>
<term>Nerve crush figure</term>
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<term>Nerve regeneration</term>
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<term>Peripheral neuropathy</term>
<term>Physiological methods</term>
<term>Present study</term>
<term>Regeneration</term>
<term>Sarcoplasmic reticulum</term>
<term>Satellite cells</term>
<term>Sciatic</term>
<term>Sciatic nerve</term>
<term>Sciatic nerve crush</term>
<term>Second week</term>
<term>Serum proteins</term>
<term>Significant increase</term>
<term>Silver impregnation</term>
<term>Skeletal muscle</term>
<term>Skeletal muscles</term>
<term>Soleus</term>
<term>Soleus muscle</term>
<term>Spheromembranous bodies</term>
<term>Spheromembranous inclusions</term>
<term>Staining fibers</term>
<term>Vacuole</term>
<term>Vesicular structures</term>
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<div type="abstract" xml:lang="en">Prolonged dosing of mice with amiodarone produced a myopathy characterized by autophagic vacuolation and phospholipid inclusions. A previous morphological study had shown that amiodarone did not affect the rate of nerve regeneration after sciatic nerve crush. In the present study, reinnervation was assessed by the reappearance of miniature endplate potentials that confirmed that axonal regeneration and motor reinnervation was not affected by amiodarone. However, there was a marked delay in the recovery of motor function in the amiodarone‐treated mice. Denervation was found to induce an extensive necrosis of muscle fibers in the deeper parts of fast‐twitch muscles. Histochemical studies showed that type 1 fibers were spared, necrosis affecting mainly type 2 fibers with relatively high oxidative enzyme activity (fast‐twitch oxidative fibers). Biochemical studies showed a significant increase in the amount of amiodarone and its metabolite in denervated muscle of amiodarone‐treated mice when compared with contralateral, normally innervated muscles.</div>
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