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Published on: June 29, 2015
Microglia, but not astrocytes, react to sciatic nerve injury in aging rats
1Department of Anatomy-510, University of Arkansas for Medical Sciences, 4301 West Markham Street, Little Rock, AR 72205, USA. sgilmore@exchange.uams.edu
Brain Research
|September 18, 1998
Summary
Peripheral nerve injury activates brain and spinal cord glial cells. Age impacts this response: young rats show both astrocyte and microglial activation, while older rats only activate microglia after sciatic nerve axotomy.
Area of Science:
- Neuroscience
- Neuroinflammation
- Glial cell biology
Background:
- Peripheral nerve axotomy triggers glial cell activation in the central nervous system.
- Microglia and astrocytes are key glial cell types involved in neuroinflammatory responses.
- Age-related differences in neuroinflammation are increasingly recognized.
Purpose of the Study:
- To investigate age-dependent glial responses (microglia and astrocytes) to peripheral nerve axotomy.
- To compare the activation patterns of astrocytes and microglia in young versus aged rats following sciatic nerve injury.
Main Methods:
- Unilateral sciatic axotomy was performed on rats aged 2 months (young) and 8 to 18 months (aged).
- Glial activation was assessed 4 days postaxotomy.
- Immunohistochemistry or similar methods were used to identify and quantify activated astrocytes and microglia in relevant spinal cord or brainstem regions.
Main Results:
- In 2-month-old rats, both astrocytes and microglia exhibited activation 4 days after sciatic axotomy.
- In rats aged 8 to 18 months, only microglial activation was observed 4 days postaxotomy; astrocyte activation was not detected.
- This indicates a differential age-dependent response of astrocytes and microglia to peripheral nerve injury.
Conclusions:
- Peripheral nerve axotomy elicits distinct age-related glial responses.
- Young rats demonstrate robust activation of both astrocytes and microglia, suggesting a comprehensive neuroinflammatory reaction.
- Aged rats exhibit a more restricted response, primarily involving microglial activation, highlighting the impact of aging on neuroinflammatory processes.

