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Updated: Jul 3, 2026

A Mouse Model of Orthopedic Surgery to Study Postoperative Cognitive Dysfunction and Tissue Regeneration
Published on: February 27, 2018
Neuroinflammation and cognitive function in aged mice following minor surgery
H A Rosczyk1, N L Sparkman, R W Johnson
1Neuroscience Program, University of Illinois, Urbana, IL 61801, USA.
Minor surgery triggers heightened neuroinflammation in aged mice, indicated by increased IL-1beta mRNA. While cognitive flexibility showed slight deficits, severe cognitive dysfunction was not observed in aged mice post-surgery.
Area of Science:
- Neuroscience
- Immunology
- Gerontology
Background:
- Postoperative cognitive dysfunction (POCD) is a common concern in elderly patients after surgery.
- Surgical trauma activates the peripheral innate immune system, releasing inflammatory mediators.
- Aged individuals exhibit heightened neuroinflammation and microglial priming, leading to exaggerated responses.
Purpose of the Study:
- To investigate if surgical trauma induces neuroinflammation and cognitive impairment in aged mice.
- To compare the neuroinflammatory and cognitive responses to surgery in adult versus aged mice.
Main Methods:
- Adult and aged mice underwent minor abdominal surgery.
- Hippocampal cytokine levels (IL-1beta mRNA) were measured 24 hours post-surgery.
- Working memory and cognitive flexibility were assessed using a Morris water maze reversal learning task.
Main Results:
- Aged mice showed significantly increased IL-1beta mRNA levels in the hippocampus post-surgery.
- Adult mice did not exhibit neuroinflammation after surgery.
- Aged mice demonstrated a trend towards perseveration, suggesting reduced cognitive flexibility, but no severe cognitive impairment.
Conclusions:
- Minor surgery elicits an exaggerated neuroinflammatory response in aged mice.
- The observed neuroinflammation in aged mice did not lead to significant cognitive impairment in the Morris water maze task.
- Age-related differences in immune response to surgical stress are evident at the neuroinflammatory level.
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