The aim of this study was to determine the MHC profile of regenerated
soleus muscles in control (C, n = 8) and hindlimb suspended rats (HS,
n = 8). After muscle degeneration was induced by injection of snake ve
nom containing notexin, male rats were either tail suspended for 21 da
ys or submitted to normal weight-bearing activity. Separation and dete
ction of MHCs by sodium dodecyl sulphate-polyarcylamide gel electropho
resis (SDS-PAGE) showed that regenerated soleus muscles from C rats co
ntained only type I and type Ila MHCs. The relative amount of type I M
HC was higher in regenerated (93.9 +/- 1.7%) than in untreated muscles
(86.5 +/- 2.3%) (P < 0.01). in the HS group, the immunohistochemical
analysis showed that the majority of regenerated myofibres reacted pos
itively with the antibody against fast MHCs. SDS-PAGE analysis demonst
rated that HS resulted in a shift toward faster MHCs in both intact an
d regenerated myofibres. Regenerated soleus muscle from HS rats contai
ned approximate to 34% type Ila MHC, approximate to 37% type IIx/d MHC
and approximate to 18% type IIb MHC, when type I MHC contributed to o
nly approximate to 12% of total myosin. The proportions of fast MHC is
oforms in regenerated muscles were higher than those recorded in untre
ated muscles. Collectively, these results suggest that the shift in th
e MHC profile associated with hindlimb unweighting in adult undamaged
soleus muscles is also related to the heterogeneity of early myoblasts
.