Spinal Cord Research Help
AboutCategoriesLatest ResearchContact
Subscribe
Spinal Cord Research Help

Making Spinal Cord Injury (SCI) Research Accessible to Everyone. Simplified summaries of the latest research, designed for patients, caregivers and anybody who's interested.

Quick Links

  • Home
  • About
  • Categories
  • Latest Research
  • Disclaimer

Contact

  • Contact Us
© 2025 Spinal Cord Research Help

All rights reserved.

  1. Home
  2. Research
  3. Neurology
  4. Molecular, Cellular and Functional Events in Axonal Sprouting after Stroke

Molecular, Cellular and Functional Events in Axonal Sprouting after Stroke

Exp Neurol, 2017 · DOI: 10.1016/j.expneurol.2016.02.007 · Published: January 1, 2017

NeurologyNeuroplasticity

Simple Explanation

Stroke often leads to long-term disability, prompting research into how the brain repairs itself. One key mechanism is axonal sprouting, where neurons form new connections after a stroke. Studies have shown that this sprouting occurs in various species, including mice, rats, primates, and humans. Inducing sprouting can improve recovery, while blocking it impairs recovery, highlighting its importance. There are three types of axonal sprouting: reactive, reparative, and unbounded. Reactive sprouting is local and part of scar formation. Reparative sprouting is longer-distance and aids recovery. Unbounded sprouting is widespread and can hinder recovery.

Study Duration
Not specified
Participants
Mice, rats, primates and humans
Evidence Level
Not specified

Key Findings

  • 1
    Post-stroke axonal sprouting occurs in mice, rats, primates and humans, suggesting it's a conserved response to brain injury.
  • 2
    Behavioral activity patterns after stroke modify the axonal sprouting response, showing that rehabilitation and activity levels influence brain rewiring.
  • 3
    The types of connections that are formed after stroke indicate three patterns of axonal sprouting after stroke: Reactive, Reparative and Unbounded Axonal Sprouting.

Research Summary

Stroke triggers axonal sprouting in areas connected to the damage, initiating within the first week and involving the growth factor GDF10. This process involves a molecular growth program with coordinated regulation of cellular components and the epigenetic modifying protein ATRX. Axonal sprouting is classified into reactive, reparative, and unbounded patterns, with reparative sprouting linked to recovery but unbounded sprouting potentially hindering it.

Practical Implications

Biomarker Development

Identifying clinically relevant markers for axonal sprouting to track and assess treatment effectiveness.

Clinical Trials for Axonal Sprouting Drugs

Moving drugs that stimulate axonal sprouting, such as anti-NogoA antibodies, into clinical trials for stroke patients.

Optimizing Therapy Timing

Carefully timing axonal sprouting therapeutics and neurorehabilitation to avoid unbounded sprouting and maximize functional recovery.

Study Limitations

  • 1
    Lack of biomarkers for axonal sprouting in animal models and humans.
  • 2
    Difficulty in translating preclinical findings of axonal sprouting drugs to clinical stroke.
  • 3
    Complexity of interactions between axonal sprouting therapies and neurorehabilitation timing.

Your Feedback

Was this summary helpful?

Back to Neurology