Literature DB >> 22446983

Active emergence from propofol general anesthesia is induced by methylphenidate.

Jessica J Chemali1, Christa J Van Dort, Emery N Brown, Ken Solt.   

Abstract

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 μg/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 δ (less than 4 Hz) to θ (4-8 Hz) and β (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.

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Year:  2012        PMID: 22446983      PMCID: PMC3339625          DOI: 10.1097/ALN.0b013e3182518bfc

Source DB:  PubMed          Journal:  Anesthesiology        ISSN: 0003-3022            Impact factor:   7.892


  25 in total

1.  General anesthetic actions in vivo strongly attenuated by a point mutation in the GABA(A) receptor beta3 subunit.

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Journal:  FASEB J       Date:  2002-12-03       Impact factor: 5.191

2.  Methylphenidate actively induces emergence from general anesthesia.

Authors:  Ken Solt; Joseph F Cotten; Aylin Cimenser; Kin F K Wong; Jessica J Chemali; Emery N Brown
Journal:  Anesthesiology       Date:  2011-10       Impact factor: 7.892

Review 3.  General anesthesia and altered states of arousal: a systems neuroscience analysis.

Authors:  Emery N Brown; Patrick L Purdon; Christa J Van Dort
Journal:  Annu Rev Neurosci       Date:  2011       Impact factor: 12.449

4.  Cholinergic reversal of isoflurane anesthesia in rats as measured by cross-approximate entropy of the electroencephalogram.

Authors:  Anthony G Hudetz; James D Wood; John P Kampine
Journal:  Anesthesiology       Date:  2003-11       Impact factor: 7.892

5.  Involvement of tuberomamillary histaminergic neurons in isoflurane anesthesia.

Authors:  Tao Luo; L Stan Leung
Journal:  Anesthesiology       Date:  2011-07       Impact factor: 7.892

6.  Norepinephrine infusion into nucleus basalis elicits microarousal in desflurane-anesthetized rats.

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Review 7.  General anesthesia, sleep, and coma.

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8.  Physostigmine reverses propofol-induced unconsciousness and attenuation of the auditory steady state response and bispectral index in human volunteers.

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10.  Antagonism of sevoflurane anaesthesia by physostigmine: effects on the auditory steady-state response and bispectral index.

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  49 in total

Review 1.  The Neurobiology of Anesthetic Emergence.

Authors:  Vijay Tarnal; Phillip E Vlisides; George A Mashour
Journal:  J Neurosurg Anesthesiol       Date:  2016-07       Impact factor: 3.956

2.  Electrical stimulation of the ventral tegmental area induces reanimation from general anesthesia.

Authors:  Ken Solt; Christa J Van Dort; Jessica J Chemali; Norman E Taylor; Jonathan D Kenny; Emery N Brown
Journal:  Anesthesiology       Date:  2014-08       Impact factor: 7.892

3.  Ageing delays emergence from general anaesthesia in rats by increasing anaesthetic sensitivity in the brain.

Authors:  J J Chemali; J D Kenny; O Olutola; N E Taylor; E Y Kimchi; P L Purdon; E N Brown; K Solt
Journal:  Br J Anaesth       Date:  2015-07       Impact factor: 9.166

4.  The Ageing Brain: Age-dependent changes in the electroencephalogram during propofol and sevoflurane general anaesthesia.

Authors:  P L Purdon; K J Pavone; O Akeju; A C Smith; A L Sampson; J Lee; D W Zhou; K Solt; E N Brown
Journal:  Br J Anaesth       Date:  2015-07       Impact factor: 9.166

Review 5.  Escape From Oblivion: Neural Mechanisms of Emergence From General Anesthesia.

Authors:  Max B Kelz; Paul S García; George A Mashour; Ken Solt
Journal:  Anesth Analg       Date:  2019-04       Impact factor: 5.108

6.  Brainstem stimulation increases functional connectivity of basal forebrain-paralimbic network in isoflurane-anesthetized rats.

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Journal:  Brain Connect       Date:  2014-09

7.  Designer receptor manipulations reveal a role of the locus coeruleus noradrenergic system in isoflurane general anesthesia.

Authors:  Elena M Vazey; Gary Aston-Jones
Journal:  Proc Natl Acad Sci U S A       Date:  2014-02-24       Impact factor: 11.205

8.  Activation of D1 dopamine receptors induces emergence from isoflurane general anesthesia.

Authors:  Norman E Taylor; Jessica J Chemali; Emery N Brown; Ken Solt
Journal:  Anesthesiology       Date:  2013-01       Impact factor: 7.892

9.  Sleep and Anesthesia Interactions: A Pharmacological Appraisal.

Authors:  Matthew T Scharf; Max B Kelz
Journal:  Curr Anesthesiol Rep       Date:  2013-03-01

10.  Competitive Antagonism of Anesthetic Action at the γ-Aminobutyric Acid Type A Receptor by a Novel Etomidate Analog with Low Intrinsic Efficacy.

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