Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Histochemical and contractile property changes during human muscle development

G C Elder1, B A Kakulas

  • 1Division of Kinesiology, Dalhousie University, Halifax, Nova Scotia, Canada.

Muscle & Nerve
|November 1, 1993
PubMed
Summary

Infant muscle development shows changes in contractile properties, particularly in plantarflexors, as muscles mature and usage increases. This study tracks these postnatal changes in muscle function and fiber type distribution.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

TGF-beta1 and TGF-beta2 expression after traumatic human spinal cord injury.

Spinal cord·2007
Same author

Sequential loss of myelin proteins during Wallerian degeneration in the human spinal cord.

Brain : a journal of neurology·2005
Same author

Neuropathology: the foundation for new treatments in spinal cord injury.

Spinal cord·2004
Same author

Prevalence of cerebral vascular amyloid-beta deposition and stroke in an aging Australian population: a postmortem study.

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia·2003
Same author

Retropulsion of intervertebral discs associated with traumatic hyperextension of the cervical spine and absence of vertebral fracture: an uncommon mechanism of spinal cord injury.

Spinal cord·2002
Same author

The mRNA of the NR1 subtype of glutamate receptor in Alzheimer's disease.

Journal of neural transmission (Vienna, Austria : 1996)·2002

Area of Science:

  • Developmental Biology
  • Physiology
  • Neuromuscular Science

Background:

  • Postnatal development involves significant changes in skeletal muscle histochemistry and contractile properties.
  • Understanding the interplay between muscle function and its developmental trajectory is crucial for assessing neuromuscular health.

Purpose of the Study:

  • To investigate the postnatal changes in histochemical and contractile properties of infant muscles.
  • To determine the influence of developing muscle function on these physiological adaptations.
  • To correlate muscle property changes with fiber type distribution during development.

Main Methods:

  • Contractile properties, including maximal twitch tension (Pt), time to peak tension (TPT), and half-relaxation times (1/2RT), were measured in plantarflexor (PF) and dorsiflexor (DF) muscles.

Related Experiment Videos

  • Measurements were taken in 19 newborns and 36 infants (5-16 months) over multiple monthly intervals.
  • Muscle fiber type distributions (Type I) were analyzed post-mortem from fetal to adult stages.
  • Main Results:

    • Time to peak tension (TPT) in plantarflexors slowed significantly from birth (77 ms) to 110-120 ms by 9-12 months, while dorsiflexors remained unchanged.
    • Soleus muscle differentiation coincided with the observed slowing of contractile properties and increased infant muscle usage.
    • A trend of higher Type I fiber percentages was noted in children compared to newborns and adults in several muscles.

    Conclusions:

    • Postnatal maturation leads to distinct changes in infant muscle contractile properties, particularly in plantarflexors, linked to increased functional use.
    • The findings suggest a correlation between muscle functional development, contractile property maturation, and shifts in fiber type distribution.
    • These insights have implications for evaluating peripheral neuromuscular function in infants and children.