Effect of microgravity on metabolic enzymes of individual muscle fibers

1990 ◽  
Vol 4 (1) ◽  
pp. 55-63 ◽  
Author(s):  
Jill K. Manchester ◽  
Maggie M.‐Y. Chi ◽  
Beverly Norris ◽  
Bernard Ferrier ◽  
Igor Krasnov ◽  
...  
Metabolism ◽  
1987 ◽  
Vol 36 (8) ◽  
pp. 761-767 ◽  
Author(s):  
Maggie M.-Y. Chi ◽  
Carol S. Hintz ◽  
Deidre McKee ◽  
Steven Felder ◽  
Natasha Grant ◽  
...  

1976 ◽  
Vol 39 (1) ◽  
pp. 84-90 ◽  
Author(s):  
E. Frank ◽  
J. K. Jansen

Foreign somatic motor nerves were made to innervate denervated gill muscles of the perch. The foreign innervation remained functional after reinnervation by the original nerve. Intracellular recordings showed that individual muscle fibers could be activated by both foreign and original neurons. Extensive foreign innervation appeared to inhibit the ability of the original nerve to reinnervate its own muscle. These studies provide evidence for a functional coexistence of appropriate and inappropriate innervation and show that foreign synapses need not be repressed by the "correct" nerve.


1984 ◽  
Vol 62 (2) ◽  
pp. 235-240 ◽  
Author(s):  
H. J. Swatland

Samples of iliotibialis anterior and pectoralis muscles were taken from five ganders (Anser domesticus). Serial transverse sections were reacted for succinate dehydrogenase (SDH) and alkali-stable adenosine triphosphatase (ATPase). The distribution of SDH activity within individual muscle fibers was measured with a scanning photometer. In many individual fibers, SDH activity was stronger in the periphery than in the axis. This gradient was steepest (−0.034 ± 0.019 absorbance units per concentric zone of 2 μm diameter measurements) in pectoralis fibers with strong SDH activity. In the pectoralis, radial gradients were correlated with fiber area so that the smallest fibers tended to have the steepest gradients of SDH activity. However, this relationship was reversed in fibers with strong ATPase and weak SDH activity in the iliotibialis anterior, and the largest fibers tended to have the steepest gradients. In all fiber types of both muscles, fibers with greater mean SDH activity tended to have steeper gradients.


1973 ◽  
Vol 61 (2) ◽  
pp. 207-221 ◽  
Author(s):  
Betty M. Twarog ◽  
Maynard M. Dewey ◽  
Tohoru Hidaka

The individual muscle fibers of the anterior byssus retractor muscle (ABRM) of Mytilus edulis L. are uninucleate, 1.2–1.8 mm in length, 5 µm in diameter, and organized into bundles 100–200 µm in diameter, surrounded by connective tissue. Some bundles run the length of the whole muscle. Adjacent muscle cell membranes are interconnected by nexuses at frequent intervals. Specialized attachments exist between muscle fibers and connective tissue. Electrical constants of the resting muscle membrane were measured with intracellular recording electrodes and both extracellular and intracellular current-passing electrodes. With an intracellular current-passing electrode, the time constant τ, was 4.3 ± 1.5 ms. With current delivered via an extracellular electrode τ was 68.3 ± 15 ms. The space constant, λ, was 1.8 mm ± 0.4. The membrane input resistance, Reff, ranged from 23 to 51 MΩ. The observations that values of τ depend on the method of passing current, and that the value of λ is large relative to fiber length and diameter are considered evidence that the individual muscle fibers are electrically interconnected within bundles in a three-dimensional network. Estimations are made of the membrane resistance, Rm, to compare the values to fast and slow striated muscle fibers and mammalian smooth muscles. The implications of this study in reinterpreting previous mechanical and electrical studies are discussed.


2017 ◽  
Vol 45 (7) ◽  
pp. 961-976 ◽  
Author(s):  
Kristin Wilson ◽  
Crystal Faelan ◽  
Janet C. Patterson-Kane ◽  
Daniel G. Rudmann ◽  
Steven A. Moore ◽  
...  

Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are neuromuscular disorders that primarily affect boys due to an X-linked mutation in the DMD gene, resulting in reduced to near absence of dystrophin or expression of truncated forms of dystrophin. Some newer therapeutic interventions aim to increase sarcolemmal dystrophin expression, and accurate dystrophin quantification is critical for demonstrating pharmacodynamic relationships in preclinical studies and clinical trials. Current challenges with measuring dystrophin include the variation in protein expression within individual muscle fibers and across whole muscle samples, the presence of preexisting dystrophin-positive revertant fibers, and trace amounts of residual dystrophin. Immunofluorescence quantification of dystrophin can overcome many of these challenges, but manual quantification of protein expression may be complicated by variations in the collection of images, reproducible scoring of fluorescent intensity, and bias introduced by manual scoring of typically only a few high-power fields. This review highlights the pathology of DMD and BMD, discusses animal models of DMD and BMD, and describes dystrophin biomarker quantitation in DMD and BMD, with several image analysis approaches, including a new automated method that evaluates protein expression of individual muscle fibers.


2000 ◽  
Vol 301 (3) ◽  
pp. 397-403 ◽  
Author(s):  
Andreas Sander ◽  
Antje Güth ◽  
Hans Rudolf Brenner ◽  
Veit Witzemann

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