Training Plan: This proposal describes a mentored 5-year research training program for the development of an independent investigator in anesthetic mechanisms. The Principal Investigator is an Assistant Professor of Anaesthesia at Harvard Medical School (HMS) and a faculty anesthesiologist at Massachusetts General Hospital (MGH), with a background in anesthetic pharmacology and electrophysiology. His mentor, Dr. Emery N. Brown, is Warren M. Zapol Professor of Anaesthesia at HMS, Professor of Computational Neuroscience in the Dept. of Brain and Cognitive Sciences at the Massachusetts Institute of Technology (MIT), and Professor of Health Sciences and Technology at HMS and MIT. With the Mentored Clinical Scientist Research Career Development Award, the Principal Investigator will acquire new knowledge and skills in systems neuroscience sufficient to develop an independent research program. He will take courses in the Dept. of Brain and Cognitive Sciences at MIT, and his research training will take place in laboratories at MGH, MIT, and the University of California, San Diego. The long-term objective of this proposal is to prepare the Principal Investigator for a successful independent career studying anesthetic mechanisms using a systems neuroscience approach. Research Plan: Accumulating evidence suggests that ascending arousal pathways in the brain promote emergence from general anesthesia (GA). Elucidating these mechanisms may lead to improved pharmacological control over the arousal states of anesthetized patients, better treatments for emergence delirium, better neurophysiological monitors to detect intraoperative awareness, and ultimately a safer and more efficient practice of anesthesiology. Our preliminary data suggest that pharmacological activation of dopaminergic and cholinergic arousal circuits during steady-state exposure to isoflurane produce distinct arousal states that are characterized by different behavioral and neurophysiological endpoints. The goal of this project is to elucidate the roles of dopaminergic and cholinergic arousal circuits in promoting emergence from GA. Using a combination of pharmacological and brain microstimulation techniques, we will probe the behavioral and neurophysiological correlates of actively induced emergence from GA.

Public Health Relevance

Many of the clinical problems related to emergence from general anesthesia (GA) have not been solved because the neural mechanisms underlying emergence have not been elucidated. The goal of this project is to elucidate the roles of dopaminergic and cholinergic arousal circuits in promoting emergence from GA. Knowledge of these mechanisms may lead to advances in clinical care including novel methods to control the arousal states of patients, better treatments for emergence delirium, and improved neurophysiological monitors that optimize anesthetic dosing and protect patients from intraoperative awareness.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08GM094394-04
Application #
8528624
Study Section
Surgery, Anesthesiology and Trauma Study Section (SAT)
Program Officer
Cole, Alison E
Project Start
2010-09-01
Project End
2014-08-31
Budget Start
2013-09-01
Budget End
2014-08-31
Support Year
4
Fiscal Year
2013
Total Cost
$102,139
Indirect Cost
$7,339
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
Kenny, Jonathan D; Chemali, Jessica J; Cotten, Joseph F et al. (2016) Physostigmine and Methylphenidate Induce Distinct Arousal States During Isoflurane General Anesthesia in Rats. Anesth Analg 123:1210-1219
Kenny, Jonathan D; Taylor, Norman E; Brown, Emery N et al. (2015) Dextroamphetamine (but Not Atomoxetine) Induces Reanimation from General Anesthesia: Implications for the Roles of Dopamine and Norepinephrine in Active Emergence. PLoS One 10:e0131914
Chemali, J J; Kenny, J D; Olutola, O et al. (2015) Ageing delays emergence from general anaesthesia in rats by increasing anaesthetic sensitivity in the brain. Br J Anaesth 115 Suppl 1:i58-i65
Solt, Ken; Van Dort, Christa J; Chemali, Jessica J et al. (2014) Electrical stimulation of the ventral tegmental area induces reanimation from general anesthesia. Anesthesiology 121:311-9
Ching, ShiNung; Liberman, Max Y; Chemali, Jessica J et al. (2013) Real-time closed-loop control in a rodent model of medically induced coma using burst suppression. Anesthesiology 119:848-60
Shanechi, Maryam M; Chemali, Jessica J; Liberman, Max et al. (2013) A brain-machine interface for control of medically-induced coma. PLoS Comput Biol 9:e1003284
Chemali, Jessica; Ching, ShiNung; Purdon, Patrick L et al. (2013) Burst suppression probability algorithms: state-space methods for tracking EEG burst suppression. J Neural Eng 10:056017
Wong, Kin Foon Kevin; Gong, Jen J; Cotten, Joseph F et al. (2013) Assessing the effects of pharmacological agents on respiratory dynamics using time-series modeling. IEEE Trans Biomed Eng 60:1118-25
Taylor, Norman E; Chemali, Jessica J; Brown, Emery N et al. (2013) Activation of D1 dopamine receptors induces emergence from isoflurane general anesthesia. Anesthesiology 118:30-9
Chemali, Jessica J; Van Dort, Christa J; Brown, Emery N et al. (2012) Active emergence from propofol general anesthesia is induced by methylphenidate. Anesthesiology 116:998-1005

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