Vj. Caiozzo et al., EFFECT OF SPACEFLIGHT ON SKELETAL-MUSCLE - MECHANICAL-PROPERTIES AND MYOSIN ISOFORM CONTENT OF A SLOW MUSCLE, Journal of applied physiology, 76(4), 1994, pp. 1764-1773
This study examined changes in contractile, biochemical, and histochem
ical properties of slow antigravity skeletal muscle after a 6-day spac
eflight mission. Twelve male Sprague-Dawley rats were randomly divided
into two groups: flight and ground-based control. Approximately 3 h a
fter the landing, in situ contractile measurements were made on the so
leus muscles of the flight animals. The control animals were studied 2
4 h later. The contractile measurements included force-velocity relati
onship, force-frequency relationship, and fatigability. Biochemical me
asurements focused on the myosin heavy chain (MHC) and myosin light ch
ain profiles. Adenosinetriphosphatase histochemistry was performed to
identify cross-sectional area of slow and fast muscle fibers and to de
termine the percent fiber type distribution. The force-velocity relati
onships of the flight muscles were altered such that maximal isometric
tension (P,) was decreased by 24% and maximal shortening velocity was
increased by 14% (P < 0.05). The force-frequency relationship of the
flight muscles was shifted to the right of the control muscles. At the
end of the 2-min fatigue test, the flight muscles generated only 34%
of P-o, whereas the control muscles generated 64% of P-o. The flight m
uscles exhibited de novo expression of the type IIx MHC isoform as wel
l as a slight decrease in the slow type I and fast type IIa MHC isofor
ms. Histochemical analyses of flight muscles demonstrated a small incr
ease in the percentage of fast type II fibers and a greater atrophy of
the slow type I fibers. The results demonstrate that contractile prop
erties of slow antigravity skeletal muscle are sensitive to the microg
ravity environment and that changes begin to occur within the Ist wk.
These changes were at least, in part, associated with changes in the a
mount and type of contractile protein expressed.