Related Experiment Video
Updated: May 6, 2026

Assessing Changes in Synaptic Plasticity Using an Awake Closed-Head Injury Model of Mild Traumatic Brain Injury
Published on: January 20, 2023
Mild and repetitive mild traumatic brain injury: Changes in microglial cells and synapses
Adna Smajkan1,2,3, Elizabeth Naranjo-Cinto1,2,4, Florence M Bareyre1,2,5
1Institute of Clinical Neuroimmunology, University Hospital, LMU Munich, Munich, Germany.
Abstract:
Mild traumatic brain injury results from external mechanical forces to the head. Repetitive mild traumatic brain injury, characterized by multiple concussive events over time, is increasingly recognized in contact sports or domestic abuse. Repetitive injuries are associated with a greater risk of cumulative deficits and chronic neurodegenerative conditions. After a period of large focus on gross morphological changes following mild traumatic brain injury and repetitive mild traumatic brain injury, recent research is exploring more subtle yet critical changes at the synaptic and microglial levels. Novel findings indicate that even a single mild traumatic brain injury can induce transient alterations in synaptic function, including increased excitatory neurotransmission and disrupted synaptic plasticity. Parallel to synaptic changes, microglial cells, the brain's resident immune cells, undergo rapid and prolonged activation after mild traumatic brain injury, including morphological transformation and functional activation. In repetitive mild traumatic brain injury, microglial priming is more pronounced, leading to sustained neuroimmune dysregulation and heightened and persistent vulnerability. In this review, we will summarize the current literature on mild traumatic brain injury and repetitive mild traumatic brain injury with a specific emphasis on microglial and synaptic changes.
Insights
Repetitive mild traumatic brain injury (mTBI) causes cumulative deficits by altering synaptic function and activating immune cells. Understanding these microglial and synaptic changes is crucial for managing chronic neurodegenerative conditions.
Area of Science:
- Neuroscience
- Immunology
- Traumatic Brain Injury Research
Background:
- Mild traumatic brain injury (mTBI) stems from external head trauma.
- Repetitive mTBI (rmTBI) is common in sports and abuse, increasing risks of neurodegeneration.
- Recent research focuses on subtle synaptic and microglial changes post-mTBI.
Purpose of the Study:
- To review current literature on mTBI and rmTBI.
- To emphasize microglial and synaptic alterations following these injuries.
Main Methods:
- Literature review of studies on mTBI and rmTBI.
- Focus on synaptic function and microglial cell activation.
- Analysis of morphological and functional changes.
Main Results:
- Single mTBI causes transient synaptic alterations, including increased excitation and disrupted plasticity.
- Microglial cells activate rapidly and persistently post-mTBI.
- rmTBI leads to pronounced microglial priming, neuroimmune dysregulation, and heightened vulnerability.
Conclusions:
- Synaptic and microglial changes are critical early events in mTBI.
- rmTBI exacerbates neuroimmune dysregulation, increasing chronic risks.
- Further research into these mechanisms is vital for therapeutic strategies.
More Related Videos
04:54Modified Mouse Model of Repetitive Mild Traumatic Brain Injury Incorporating Thinned-Skull Window and Fluid Percussion
Published on: April 19, 2024
08:27Development of an Uncomplicated Mild Traumatic Brain Injury Model Modified by Weight-Drop Method and Evidenced by Magnetic Resonance Imaging
Published on: April 11, 2025