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Meakins-Christie Laboratories, Royal Victoria Hospital, McGill University, Montreal, Quebec, Canada H2X 2P2
The object of this study was to investigate
how changes in the contractile state of smooth muscle would modify
oscillatory mechanics of tracheal muscle and lung parenchyma during
agonist challenge. Guinea pig tracheal and parenchymal lung strips were suspended in an organ bath. Measurements of length
(L) and tension (T) were recorded
during sinusoidal oscillations under baseline conditions and after
challenge with 1 mM ACh. Measurements were also obtained in strips
pretreated with the calmodulin inhibitor calmidazolium (Cmz) or
staurosporine (Stauro), a protein kinase C inhibitor. Elastance (E) and
resistance (R) were calculated by fitting changes in T,
L, and
L/
t
to the equation of motion. Hysteresivity (
) was obtained from the
following equation:
= (R/E)2
f,
where f is frequency. Finally, maximal
unloaded shortening velocity during electrical field stimulation was
measured in Cmz-pretreated and control tracheal strips. In tracheal
strips, pretreatment with Cmz caused a significant decrease in the
response to ACh challenge and in maximal unloaded shortening velocity
measured during electrical field stimulation; Stauro decreased the T,
E, and R response to ACh. In parenchymal strips, Cmz decreased the
response, whereas Stauro had no effect. These results suggest that
modifications in the contractile state of the smooth muscle are
reflected in changes in the hysteretic behavior and that T and
may
be controlled independently. Second, inasmuch as changes in
were
similar in parenchymal and tracheal strips, the contractile element is
implicated as the structure responsible for constriction-induced changes in the mechanical behavior of the lung periphery.
calmodulin; protein kinase C; smooth muscle contraction; elastance; resistance
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