Rapid Eye Movement Sleep Debt Accrues in Mice Exposed to Volatile Anesthetics

Author:

Pick Jeremy1,Chen Yihan2,Moore Jason T.3,Sun Yi4,Wyner Abraham J.5,Friedman Eliot B.6,Kelz Max B.7

Affiliation:

1. Medical Student, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania.

2. Undergraduate, University of Pennsylvania, Philadelphia, Pennsylvania.

3. Graduate Student, Departments of Neuroscience and Anesthesiology and Critical Care, University of Pennsylvania.

4. Research Specialist, Department of Anesthesiology and Critical Care, University of Pennsylvania School of Medicine.

5. Associate Professor, Department of Statistics, The Wharton School, University of Pennsylvania.

6. Instructor, Department of Medicine, Center for Sleep and Circadian Neurobiology, Institute for Translational Medicine and Therapeutics, University of Pennsylvania School of Medicine.

7. Assistant Professor, Department of Anesthesiology and Critical Care, Center for Sleep and Circadian Neurobiology, Institute for Translational Medicine and Therapeutics, University of Pennsylvania School of Medicine.

Abstract

Background General anesthesia has been likened to a state in which anesthetized subjects are locked out of access to both rapid eye movement (REM) sleep and wakefulness. Were this true for all anesthetics, a significant REM rebound after anesthetic exposure might be expected. However, for the intravenous anesthetic propofol, studies demonstrate that no sleep debt accrues. Moreover, preexisting sleep debts dissipate during propofol anesthesia. To determine whether these effects are specific to propofol or are typical of volatile anesthetics, the authors tested the hypothesis that REM sleep debt would accrue in rodents anesthetized with volatile anesthetics. Methods Electroencephalographic and electromyographic electrodes were implanted in 10 mice. After 9-11 days of recovery and habituation to a 12 h:12 h light-dark cycle, baseline states of wakefulness, nonrapid eye movement sleep, and REM sleep were recorded in mice exposed to 6 h of an oxygen control and on separate days to 6 h of isoflurane, sevoflurane, or halothane in oxygen. All exposures were conducted at the onset of light. Results Mice in all three anesthetized groups exhibited a significant doubling of REM sleep during the first 6 h of the dark phase of the circadian schedule, whereas only mice exposed to halothane displayed a significant increase in nonrapid eye movement sleep that peaked at 152% of baseline. Conclusion REM sleep rebound after exposure to volatile anesthetics suggests that these volatile anesthetics do not fully substitute for natural sleep. This result contrasts with the published actions of propofol for which no REM sleep rebound occurred.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Anesthesiology and Pain Medicine

Reference65 articles.

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