[Purpose] Although the shapes observed in myofiber cross-sections have been subjectively identified as polygonal, precise methodologies to classify such shapes have not been elucidated previously. Therefore, we aimed to determine the approximate shapes found in myofiber cross-sections, and to elucidate their relationship with the myofiber cross-sectional area. [Materials and Methods] Soleus muscles of five 11-week-old male Wistar rats were collected as specimens. The muscle specimens were rapid-frozen in isopentane-cooled in dry ice and acetone-and sliced into 10-μm slices in a cryostat and stained with hematoxylin-eosin. The NIH ImageJ software was used to analyze the number of corners that were counted according to the proposed criteria and the myofiber cross-sectional areas of 500 myofibers. [Results] In assessments of the approximate shapes of myofiber cross-sections, the proportion of pentagons was 41%, which was the highest among polygons. A weak positive correlation was noted between the corner count and myofiber cross-sectional area, which indicated that polygons with more corners were associated with a larger myofiber cross-sectional area. [Conclusion] The myofiber cross-sections of the soleus muscle were considered to frequently show an approximately pentagonal shape. Moreover, a correlation was observed between the myofiber cross-section shape and myofiber cross-sectional area, suggesting that the area was also associated with the relevant functional features.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636916 | PMC |
http://dx.doi.org/10.1589/jpts.33.931 | DOI Listing |
Metabolites
December 2024
Department of Molecular Biology and Genetics, Lopukhin Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency, 119435 Moscow, Russia.
Background: Data on the genetic factors contributing to inter-individual variability in muscle fiber size are limited. Recent research has demonstrated that mice lacking the Arkadia (RNF111) N-terminal-like PKA signaling regulator 2N (; also known as ) gene exhibit reduced muscle fiber size, contraction force, and exercise capacity, along with defects in calcium handling within fast-twitch muscle fibers. However, the role of the gene in human muscle physiology, and particularly in athletic populations, remains poorly understood.
View Article and Find Full Text PDFMar Drugs
December 2024
Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul 03722, Republic of Korea.
The objective of this study was to examine whether fucosterol, a phytosterol of marine algae, could ameliorate skeletal muscle atrophy in tumor necrosis factor-alpha (TNF-α)-treated C2C12 myotubes and in immobilization-induced C57BL/6J mice. Male C57BL6J mice were immobilized for 1 week to induce skeletal muscle atrophy. Following immobilization, the mice were administrated orally with saline or fucosterol (10 or 30 mg/kg/day) for 1 week.
View Article and Find Full Text PDFFront Neurol
December 2024
Department of Surgery, Division of Otolaryngology, University of Wisconsin, Madison, WI, United States.
Introduction: Down syndrome (DS) is associated with difficulties with feeding during infancy and childhood. Weaning, or transitioning from nursing to independent deglutition, requires developmental progression in tongue function. However, little is known about whether postnatal tongue muscle maturation is impacted in DS.
View Article and Find Full Text PDFFront Physiol
December 2024
Emergency Center, Hubei Clinical Research Center for Emergency and Resuscitaion, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Background: Skeletal muscle atrophy significantly affects quality of life and has socio-economic and health implications. This study evaluates the effects of entacapone (ENT) on skeletal muscle atrophy linked with oxidative stress and proteolysis.
Methods: C2C12 cells were treated with dexamethasone (Dex) to simulate muscle atrophy.
Curr Stem Cell Res Ther
December 2024
Center for Rehabilitation Medicine, Rehabilitation & Sports Medicine Research Institute of Zhejiang Province, Department of Rehabilitation Medicine, Zhejiang Provincial People's Hospital(Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, Zhejiang, China.
Background: Skeletal muscle atrophy in myotonic dystrophy type 1 (DM1) is caused by abnormal skeletal muscle satellite cell (SSC) proliferation due to increased glycolysis, which impairs muscle regeneration. In DM1, RNA foci sequester muscleblind-like protein 1 (MBNL1) in the nucleus, inhibiting its role in regulating SSC proliferation. Aerobic training reduces glycolysis and increases SSC proliferation and muscle fiber volume.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!