Active Emergence from Propofol General Anesthesia Is Induced by Methylphenidate

Background: A recent study showed that methylphenidate induces emergence from isoflurane general anesthesia. Isoflurane and propofol are general anesthetics that may have distinct molecular mechanisms of action. The objective of this study was to test the hypothesis that methylphenidate actively induces emergence from propofol general anesthesia. Methods: Using adult rats, the effect of methylphenidate on time to emergence after a single bolus of propofol was determined. The ability of methylphenidate to restore righting during a continuous target-controlled infusion (TCI) of propofol was also tested. In a separate group of rats, a TCI of propofol was established and spectral analysis was performed on electroencephalogram recordings taken before and after methylphenidate administration. Results: Methylphenidate decreased median time to emergence after a single dose of propofol from 735 s (95% CI: 598–897 s, n = 6) to 448 s (95% CI: 371–495 s, n = 6). The difference was statistically significant (P = 0.0051). During continuous propofol anesthesia with a median final target plasma concentration of 4.0 &mgr;g/ml (95% CI: 3.2–4.6, n = 6), none of the rats exhibited purposeful movements after injection of normal saline. After methylphenidate, however, all six rats promptly exhibited arousal and had restoration of righting with a median time of 82 s (95% CI: 30–166 s). Spectral analysis of electroencephalogram data demonstrated a shift in peak power from &dgr; (less than 4 Hz) to &thgr; (4–8 Hz) and &bgr; (12–30 Hz) after administration of methylphenidate, indicating arousal in 4/4 rats. Conclusions: Methylphenidate decreases time to emergence after a single dose of propofol, and induces emergence during continuous propofol anesthesia in rats. Further study is warranted to test the hypothesis that methylphenidate induces emergence from propofol general anesthesia in humans.

[1]  M. Degroot,et al.  Probability and Statistics , 2021, Examining an Operational Approach to Teaching Probability.

[2]  P C Vijn,et al.  I.v. anaesthesia and EEG burst suppression in rats: bolus injections and closed-loop infusions. , 1998, British journal of anaesthesia.

[3]  P Fiset,et al.  Physostigmine reverses propofol-induced unconsciousness and attenuation of the auditory steady state response and bispectral index in human volunteers. , 2000, Anesthesiology.

[4]  E. Brown,et al.  General anesthesia, sleep, and coma. , 2010, The New England journal of medicine.

[5]  Masashi Yanagisawa,et al.  An essential role for orexins in emergence from general anesthesia , 2008, Proceedings of the National Academy of Sciences.

[6]  Siveshigan Pillay,et al.  Norepinephrine Infusion into Nucleus Basalis Elicits Microarousal in Desflurane-anesthetized Rats , 2011, Anesthesiology.

[7]  P. Lalley,et al.  Dopamine1 receptor agonists reverse opioid respiratory network depression, increase CO2 reactivity , 2004, Respiratory Physiology & Neurobiology.

[8]  Anthony G Hudetz,et al.  Cholinergic Reversal of Isoflurane Anesthesia in Rats as Measured by Cross-approximate Entropy of the Electroencephalogram , 2003, Anesthesiology.

[9]  Michael T Alkire,et al.  Thalamic Microinjection of Nicotine Reverses Sevoflurane-induced Loss of Righting Reflex in the Rat , 2007, Anesthesiology.

[10]  G. Plourde,et al.  Antagonism of sevoflurane anaesthesia by physostigmine: effects on the auditory steady-state response and bispectral index. , 2003, British journal of anaesthesia.

[11]  L. Leung,et al.  Involvement of Tuberomamillary Histaminergic Neurons in Isoflurane Anesthesia , 2011, Anesthesiology.

[12]  Joseph F. Cotten,et al.  Methoxycarbonyl-etomidate: A Novel Rapidly Metabolized and Ultra–short-acting Etomidate Analogue that Does Not Produce Prolonged Adrenocortical Suppression , 2009, Anesthesiology.

[13]  P. Lalley,et al.  D1-dopamine receptor agonists prevent and reverse opiate depression of breathing but not antinociception in the cat. , 2005, American journal of physiology. Regulatory, integrative and comparative physiology.

[14]  David J. Sheskin,et al.  Handbook of Parametric and Nonparametric Statistical Procedures , 1997 .

[15]  Tao Luo,et al.  Basal Forebrain Histaminergic Transmission Modulates Electroencephalographic Activity and Emergence from Isoflurane Anesthesia , 2009, Anesthesiology.

[16]  S. Cheetham,et al.  The neuropharmacology of ADHD drugs in vivo: Insights on efficacy and safety , 2009, Neuropharmacology.

[17]  P. Lalley D1/D2-dopamine receptor agonist dihydrexidine stimulates inspiratory motor output and depresses medullary expiratory neurons. , 2009, American journal of physiology. Regulatory, integrative and comparative physiology.

[18]  Meindert Danhof,et al.  Allometric relationships between the pharmacokinetics of propofol in rats, children and adults. , 2005, British journal of clinical pharmacology.

[19]  K. Hanaoka,et al.  [General anesthesia for two patients taking methylphenidate (Ritalin)]. , 2008, Masui. The Japanese journal of anesthesiology.

[20]  D. Ririe,et al.  Unexpected interaction of methylphenidate (Ritalin®) with anaesthetic agents , 1997, Paediatric anaesthesia.

[21]  D. Sheskin Handbook of Parametric and Nonparametric Statistical Procedures: Third Edition , 2000 .

[22]  Gwilym M. Jenkins,et al.  Time series analysis, forecasting and control , 1972 .

[23]  E. Eger,et al.  &bgr;3-Containing Gamma-Aminobutyric AcidA Receptors Are Not Major Targets for the Amnesic and Immobilizing Actions of Isoflurane , 2005, Anesthesia and analgesia.

[24]  B. Antkowiak,et al.  General anesthetic actions in vivo strongly attenuated by a point mutation in the GABAA receptor β3 subunit , 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[25]  E. Brown,et al.  General anesthesia and altered states of arousal: a systems neuroscience analysis. , 2011, Annual review of neuroscience.

[26]  M. Maze,et al.  The Involvement of Hypothalamic Sleep Pathways in General Anesthesia: Testing the Hypothesis Using the GABAA Receptor β3N265M Knock-In Mouse , 2009, The Journal of Neuroscience.

[27]  N. Franks General anaesthesia: from molecular targets to neuronal pathways of sleep and arousal , 2008, Nature Reviews Neuroscience.

[28]  Partha P. Mitra,et al.  Chronux: A platform for analyzing neural signals , 2010, Journal of Neuroscience Methods.

[29]  Emery N. Brown,et al.  Methylphenidate Actively Induces Emergence from General Anesthesia , 2011, Anesthesiology.