Key result
Hypergravity alters rat muscle spindle MyHC expression, increasing MyHC I and alpha-cardiac isoforms.
Why the study?
Does 19 days of hypergravity alter the expression of myosin heavy chain isoforms in rat soleus muscle spindles?
Does 19 days of hypergravity alter the expression of myosin heavy chain isoforms in rat soleus muscle spindles?
Hypergravity alters myosin heavy chain isoform expression in rat soleus muscle spindles, inducing changes inverse to those seen in hypogravity.
Supports gravity-dependent myosin plasticity in rat spindles; hypothesis-generating for human spaceflight muscle countermeasures.
The aim of this study was to determine whether a period of 19 days in hypergravity was long enough to induce changes in the expression of myosin heavy chain (MyHC) isoforms in the muscle spindles. The soleus muscle of 10 male Wistar rats (control: CONT, n=5; hypergravity: HG, n=5) was frozen, cut into serial sections, and labeled with antibodies against MyHCs: I, IIA, IIA + IIX + IIB, slow-tonic, and alpha-cardiac. Forty CONT and 45 HG spindles were analyzed. The results from HG spindles compared to CONT showed that there was no change in the cross-sectional area of intrafusal fibers. However, along the entire length of B1 fibers, the expression of both MyHC I and alpha-cardiac was increased significantly, whereas the labeling against MyHC IIA and MyHC slow-tonic was decreased. In B2 fibers, the labeling against MyHC IIA (region A), slow-tonic (region A), and fast myosins (regions A-C) was statistically decreased. In chain fibers, the labeling against both MyHC IIA and fast MyHC was reduced significantly. We conclude that hypergravity has a real impact on the MyHC content in the muscle spindles and induces some inverse changes of those observed in hypogravity for MyHCs I, alpha-cardiac, and slow-tonic.
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Picquet et al. (2003) studied this question. Hypergravity vs. Control was evaluated on Expression of myosin heavy chain (MyHC) isoforms in the muscle spindles. Hypergravity for 19 days significantly altered myosin heavy chain isoform expression in rat muscle spindles, increasing MyHC I and alpha-cardiac while decreasing MyHC IIA and slow-tonic.
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