Related Experiment Videos
Volatile anaesthetics as central nervous system excitants
Annals of the Academy of Medicine, Singapore
|November 1, 1994
Summary
Volatile anesthetics (VAs) can excite the central nervous system (CNS), contrary to their depressant effects. Studies show VAs like isoflurane and enflurane induce opisthotonus in mice, indicating CNS stimulation.
Area of Science:
- Neuroscience
- Anesthesiology
- Pharmacology
Background:
- Volatile anesthetics (VAs) are primarily known as central nervous system (CNS) depressants.
- Emerging evidence suggests VAs also exhibit CNS excitatory actions.
Purpose of the Study:
- To review behavioral evidence supporting the CNS excitatory actions of VAs.
- To investigate the mechanisms and correlates of VA-induced CNS excitation.
Main Methods:
- Observation of anesthetic-induced opisthotonus (OP) in mice.
- Correlation analysis of OP incidence with anesthetic properties (e.g., blood/gas partition coefficient).
- Assessment of receptor mediation (NMDA, glycine, GABAA) and neurochemical changes (methionine-enkephalin) in enflurane-induced OP.
- Evaluation of open-field activity and active avoidance learning post-anesthesia.
Main Results:
- The incidence of VA-induced opisthotonus (OP) in mice correlates inversely with the blood/gas partition coefficient, suggesting shorter induction times lead to higher OP incidence.
- Isoflurane induced higher OP incidence than enflurane in mice, contrasting with human clinical observations.
- Enflurane-induced OP appears mediated by NMDA and glycine receptors, not GABAA receptors.
- Methionine-enkephalin immunoreactivity in the hippocampus correlates with OP incidence across mouse strains.
- Open-field activity increased post-anesthesia with enflurane and isoflurane.
Conclusions:
- Volatile anesthetics exhibit significant CNS excitatory properties, evidenced by behaviors like opisthotonus in mice.
- The incidence and mechanisms of VA-induced CNS excitation vary between anesthetic agents and species.
- Further research is needed to fully elucidate the excitatory pathways of VAs and their clinical implications.