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dc.contributor.authorSolt, Ken
dc.contributor.authorCotten, Joseph F.
dc.contributor.authorCimenser, Aylin
dc.contributor.authorWong, Kin F. K.
dc.contributor.authorChemali, Jessica J.
dc.contributor.authorBrown, Emery N.
dc.date.accessioned2014-05-01T16:50:11Z
dc.date.available2014-05-01T16:50:11Z
dc.date.issued2011-10
dc.date.submitted2011-02
dc.identifier.issn0003-3022
dc.identifier.urihttp://hdl.handle.net/1721.1/86332
dc.description.abstractBackground: Although accumulating evidence suggests that arousal pathways in the brain play important roles in emergence from general anesthesia, the roles of monoaminergic arousal circuits are unclear. In this study, the authors tested the hypothesis that methylphenidate (an inhibitor of dopamine and norepinephrine transporters) induces emergence from isoflurane general anesthesia. Methods: Using adult rats, the authors tested the effect of intravenous methylphenidate on time to emergence from isoflurane general anesthesia. They then performed experiments to test separately for methylphenidate-induced changes in arousal and changes in minute ventilation. A dose–response study was performed to test for methylphenidate-induced restoration of righting during continuous isoflurane general anesthesia. Surface electroencephalogram recordings were performed to observe neurophysiological changes. Plethysmography recordings and arterial blood gas analysis were performed to assess methylphenidate-induced changes in respiratory function. Intravenous droperidol was administered to test for inhibition of methylphenidate's actions. Results: Methylphenidate decreased median time to emergence from 280 to 91 s. The median difference in time to emergence without methylphenidate compared with administration of methylphenidate was 200 [155–331] s (median, [95% CI]). During continuous inhalation of isoflurane, methylphenidate induced return of righting in a dose-dependent manner, induced a shift in electroencephalogram power from delta (less than 4 Hz) to theta (4–8 Hz), and induced an increase in minute ventilation. Administration of intravenous droperidol (0.5 mg/kg) before intravenous methylphenidate (5 mg/kg) largely inhibited methylphenidate-induced emergence behavior, electroencephalogram changes, and changes in minute ventilation. Conclusions: Methylphenidate actively induces emergence from isoflurane general anesthesia by increasing arousal and respiratory drive, possibly through activation of dopaminergic and adrenergic arousal circuits. The authors' findings suggest that methylphenidate may be useful clinically as an agent to reverse general anesthetic-induced unconsciousness and respiratory depression at the end of surgery.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant DP1-OD003646)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant K08-GM094394)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant K08-GM083216)en_US
dc.description.sponsorshipMassachusetts General Hospital. Dept. of Anesthesia and Critical Careen_US
dc.language.isoen_US
dc.publisherOvid Technologies (Wolters Kluwer) - Lippincott Williams & Wilkinsen_US
dc.relation.isversionofhttp://dx.doi.org/10.1097/ALN.0b013e31822e92e5en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleMethylphenidate Actively Induces Emergence from General Anesthesiaen_US
dc.typeArticleen_US
dc.identifier.citationSolt, Ken, Joseph F. Cotten, Aylin Cimenser, Kin F. K. Wong, Jessica J. Chemali, and Emery N. Brown. “Methylphenidate Actively Induces Emergence from General Anesthesia.” Anesthesiology 115, no. 4 (October 2011): 791–803.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.mitauthorSolt, Kenen_US
dc.contributor.mitauthorBrown, Emery N.en_US
dc.relation.journalAnesthesiologyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsSolt, Ken; Cotten, Joseph F.; Cimenser, Aylin; Wong, Kin F. K.; Chemali, Jessica J.; Brown, Emery N.en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-5328-2062
dc.identifier.orcidhttps://orcid.org/0000-0003-2668-7819
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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