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1 Laboratoire d'Optique
Appliquée-Ecole Polytechnique,
We investigated
the hypothesis that diaphragm compliance was abnormal in
cardiomyopathic Syrian hamsters (CSH), an experimental model of
myopathy. The passive elastic properties of isolated diaphragm muscles
were analyzed at both the muscle and sarcomere levels. We used the
following passive exponential relationship between stress (
) and
strain (
):
= (Eo/
)
(e
1), where Eo is the initial
elastic modulus and
is the stiffness constant. Immunocytochemistry
procedures were used to analyze the distribution of two key elastic
components of muscle, extracellular collagen and intracellular titin
elastic components, as well as the extracellular matrix glycoprotein
laminin. Muscle and sarcomere values of
were nearly twofold lower
in CSH (8.7 ± 1.9 and 8.3 ± 1.4, respectively) than in control
animals (19.7 ± 1.7 and 16.8 ± 2.1, respectively)
(P < 0.01 for each). Compared with
controls, Eo was higher in CSH.
Sarcomere slack length was significantly longer in CSH than in control
animals (2.1 ± 0.1 vs. 1.9 ± 0.1 µm,
P < 0.05). The surface area of
collagen I was significantly larger in CSH (17.4 ± 1.8%) than in
control animals (12.4 ± 0.7%, P < 0.05). There was no change in the distribution of titin or laminin
labelings between the groups. These results demonstrate increased
diaphragm compliance in cardiomyopathic hamsters. The increase in CSH
diaphragm compliance was observed despite an increase in the surface
area of collagen and was not associated with an abnormal distribution
of titin or laminin.
myopathy; skeletal muscle; stiffness; extracellullar matrix; titin
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