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 Concept Videos

Neurons: The Axon01:21

Neurons: The Axon

Axons are long, cytoplasmic processes of nerve cells capable of propagating electrical impulses known as action potentials. The cytoplasm or axoplasm of an axon contains neurofibrils, neurotubules, small vesicles, lysosomes, mitochondria, and various enzymes, all encased within the axolemma, the plasma membrane of the axon.
The axon attaches to the cell body at a cone-shaped elevation called the axon hillock. The initial part of the axon, closest to the hillock, is known as the initial segment.
Neurogenesis and Regeneration of Nervous Tissue01:15

Neurogenesis and Regeneration of Nervous Tissue

In the CNS, neurogenesis, the birth of new neurons from stem cells, is limited to the hippocampus in adults. In other regions of the brain and spinal cord, neurogenesis is almost non-existent due to inhibitory influences from neuroglia, especially oligodendrocytes, and the absence of growth-stimulating cues. The myelin produced by oligodendrocytes in the CNS inhibits neuronal regeneration. Furthermore, astrocytes proliferate rapidly after neuronal damage, forming scar tissue that physically...
Nervous Tissue: Myelin01:25

Nervous Tissue: Myelin

The myelin sheath is a multilayered lipid and protein covering that insulates the axon of a neuron, enhancing the speed of nerve impulse conduction. Axons without this sheath are referred to as unmyelinated. Two types of neuroglia, Schwann cells in the peripheral nervous system (PNS) and oligodendrocytes in the central nervous system (CNS) are responsible for producing myelin sheaths.
Schwann cells begin to form myelin sheaths around axons during fetal development. They wrap around a small...

You might also read

Related Articles

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

Sort by
Same author

Association of ambient air pollution with cognitive functioning and markers of structural brain damage: The Maastricht study.

Environment international·2024
Same author

A (Sub)field Guide to Quality Control in Hippocampal Subfield Segmentation on Highresolution T<sub>2</sub>-weighted MRI.

bioRxiv : the preprint server for biology·2023
Same author

Cognitive Functioning in Survivors of Hematopoietic Stem Cell Transplantation Compared With a Matched General Population Sample-The Maastricht Observational Study of Late Effects After Stem Cell trAnsplantation Study.

Transplantation and cellular therapy·2023
Same author

School Achievement in Early Adolescence Is Associated With Students' Self-Perceived Executive Functions.

Frontiers in psychology·2022
Same author

Prenatal diagnosis of rhombencephalosynapsis: neuroimaging features and severity of vermian anomaly.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2021
Same author

Sex differences in self-regulation in early, middle and late adolescence: A large-scale cross-sectional study.

PloS one·2020

Related Experiment Video

Updated: Jun 5, 2026

Imaging and Analysis of Neurofilament Transport in Excised Mouse Tibial Nerve
09:52

Imaging and Analysis of Neurofilament Transport in Excised Mouse Tibial Nerve

Published on: August 31, 2020

Age differences in speed of processing are partially mediated by differences in axonal integrity.

S Burgmans1, E H B M Gronenschild, Y Fandakova

  • 1Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands.

Neuroimage
|January 15, 2011
PubMed
Summary

White matter integrity decline, specifically axonal integrity, partially explains age-related slowing in processing speed. This brain aging effect is more pronounced in posterior brain regions.

More Related Videos

A Method for Investigating Age-related Differences in the Functional Connectivity of Cognitive Control Networks Associated with Dimensional Change Card Sort Performance
09:01

A Method for Investigating Age-related Differences in the Functional Connectivity of Cognitive Control Networks Associated with Dimensional Change Card Sort Performance

Published on: May 7, 2014

An Ex Vivo Laser-induced Spinal Cord Injury Model to Assess Mechanisms of Axonal Degeneration in Real-time
11:18

An Ex Vivo Laser-induced Spinal Cord Injury Model to Assess Mechanisms of Axonal Degeneration in Real-time

Published on: November 25, 2014

Related Experiment Videos

Last Updated: Jun 5, 2026

Imaging and Analysis of Neurofilament Transport in Excised Mouse Tibial Nerve
09:52

Imaging and Analysis of Neurofilament Transport in Excised Mouse Tibial Nerve

Published on: August 31, 2020

A Method for Investigating Age-related Differences in the Functional Connectivity of Cognitive Control Networks Associated with Dimensional Change Card Sort Performance
09:01

A Method for Investigating Age-related Differences in the Functional Connectivity of Cognitive Control Networks Associated with Dimensional Change Card Sort Performance

Published on: May 7, 2014

An Ex Vivo Laser-induced Spinal Cord Injury Model to Assess Mechanisms of Axonal Degeneration in Real-time
11:18

An Ex Vivo Laser-induced Spinal Cord Injury Model to Assess Mechanisms of Axonal Degeneration in Real-time

Published on: November 25, 2014

Area of Science:

  • Neuroscience
  • Cognitive Psychology
  • Aging Research

Background:

  • Advanced age is linked to brain structure and cognitive function decline.
  • The specific brain aging mechanisms underlying cognitive deficits remain unclear.
  • White matter integrity is crucial for cognitive performance and vulnerable to aging.

Purpose of the Study:

  • To investigate if white matter integrity differences mediate age-related cognitive declines.
  • To examine the relationship between white matter integrity and executive functioning and processing speed.
  • To determine if vascular risk factors influence these age-related brain-cognition associations.

Main Methods:

  • Latent variable analyses were used to assess age differences in white matter integrity.
  • Diffusion-related measures of white matter integrity were compared to volumes and hyperintensities.
  • Mediation analyses examined the role of white matter integrity in age-related cognitive performance.
  • Participants included healthy adults aged 50-81, with and without hypertension.

Main Results:

  • Diffusion-related latent variables showed greater age differences than volumetric measures.
  • Reduced white matter linear anisotropy partially mediated age-related declines in processing speed.
  • This mediation effect was significant in posterior brain regions and stronger for cognitive measures of processing speed.
  • Hypertension status did not alter the observed results.

Conclusions:

  • Deterioration of axonal integrity and connectivity underlies age-related slowing of information processing in healthy adults.
  • White matter integrity is a key mediator of cognitive aging, particularly in posterior brain areas.
  • These findings highlight the importance of maintaining white matter health for cognitive function in aging.