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1 Department of Physical
Therapy,
This study was designed to test the hypothesis
that myosin heavy (MHC) and light chain (MLC) plasticity resulting from
hindlimb suspension (HS) is an age-dependent process. By using an
electrophoretic technique, the distribution of MHC and MLC isoforms was
quantitatively evaluated in the soleus muscles from 3- or 12-wk-old
rats after 1-3 wk of HS treatment was maintained. In normal 12- and 15-wk-old rats, the soleus muscles contained a predominance of
MHCI (~94%) with small amounts
of MHCIIa, but not
MHCIId or
MHCIIb. The suspended muscles of
adult rats were characterized by the appearance of MHCIIb and
MHCIId, the latter reaching ~6%
after 3 wk of HS treatment. In contrast to changes in MHC, HS did not
induce a transition in the MLC pattern in the soleus muscles from adult
rats. Compared with adult rats, in juveniles HS had a much more
pronounced effect on the shift toward faster MHC and MLC isoform
expression. The soleus muscles of 6-wk-old rats after 3 wk of HS were
composed of 37.0% MHCI, 19.1%
MHCIIa, 23.7%
MHCIId, and 20.2%
MHCIIb. Changes in MLC isoforms
consisted of an increase in MLC1f
and MLC2f concomitant with a
decrease in MLC2s. These results
indicate the existence of a differential effect of HS on MHC and MLC
transitions that appears to be age dependent. They also suggest that
the suspended soleus muscles from young rats may acquire the intrinsic
contractile properties that are intermediate between those in the
normal soleus and typical fast-twitch skeletal muscles.
development; hindlimb suspension; transition
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