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Object memory in young and aged mice after sevoflurane anaesthesia
Andreas Wiklund1, Sylvie Granon, Philippe Faure
1Department of Anaesthesiology, Surgical Services and Intensive Care Medicine, Karolinska University Hospital, Stockholm, Sweden. andreas.wiklund@karolinska.se
Neuroreport
|September 10, 2009
Summary
Sevoflurane anesthesia impairs episodic-like memory in mice, regardless of age or beta2 receptor function. This finding highlights anesthesia
Area of Science:
- Neuroscience
- Anesthesiology
- Cognitive Science
Background:
- Post-surgical cognitive dysfunction, particularly memory impairment, affects patients, especially the elderly.
- The role of specific anesthetic agents like sevoflurane in memory deficits requires further investigation.
- Nicotinic cholinergic pathways, involving beta2 receptors, are crucial for learning and memory.
Purpose of the Study:
- To investigate the impact of sevoflurane anesthesia on episodic-like memory in young and aged mice.
- To determine if beta2 receptor-mediated nicotinic cholinergic neurotransmission influences sevoflurane-induced memory impairment.
Main Methods:
- Object recognition memory task was used to assess memory retention in mice.
- Mice were exposed to sevoflurane anesthesia (2.6% for 2 hours) or a sham procedure immediately after training.
- Experiments included young and aged wild-type mice, as well as beta2 knockout (beta2KO) mice.
Main Results:
- Mice subjected to sevoflurane anesthesia exhibited significant impairment in object memory retention compared to non-anesthetized controls.
- Memory deficits were observed in both young and aged wild-type mice after sevoflurane exposure.
- Sevoflurane-induced memory impairment occurred irrespective of the presence or absence of functional beta2 receptors (in beta2KO mice).
Conclusions:
- Sevoflurane anesthesia induces significant episodic-like memory impairment in mice.
- This memory impairment is independent of the beta2 receptor-mediated nicotinic cholinergic pathway.
- The findings suggest a broader impact of sevoflurane on memory mechanisms beyond the nicotinic cholinergic system.
