Bupivacaine-induced regeneration was studied in the rat soleus muscle in the presence or absence
of innervation, in the presence of tetrodotoxin (TTX)-induced block of nerve impulse
conduction, and/or in the presence of vinblastine-induced block of nerve axoplasmic flow.
Part of experiments were carried out on tenotomized muscles. Regenerated muscles were
analysed for myosin heavy chain (MHC) composition 14 days after bupivacaine injection. In
TTX-paralysed-regenerated muscles type 1 and type 2A MHC isoforms were not expressed.
In denervated-regenerated muscles type 1 isoform was lacking, while all fast isoforms (2A,
2B, 2X) were expressed. Tenotomy alone increased type 2A fibres, but did not modify the effects
of surgical or functional denervation. Vinblastine-block caused up-regulation of 2A isoform
expression in non-tenotomized muscles. The results confirm the essential role played by
neuromotor impulses for type 1 and type 2A isoform expression. They also support the
hypothesis that axoplasmic flow carries some chemical factor inhibiting 2A isoform expression
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