Resting-state Network-specific Breakdown of Functional Connectivity during Ketamine Alteration of Consciousness in Volunteers

被引:142
作者
Bonhomme, Vincent [1 ,2 ,3 ,6 ]
Vanhaudenhuyse, Audrey [2 ,3 ,4 ,5 ]
Demertzi, Athena [2 ,3 ,4 ,12 ]
Bruno, Marie-Aurelie [2 ,3 ,4 ]
Jaquet, Oceane [1 ,2 ,6 ]
Bahri, Mohamed Ali [2 ,3 ,4 ]
Plenevaux, Alain [4 ]
Boly, Melanie [8 ]
Boveroux, Pierre [6 ,9 ,10 ]
Soddu, Andrea [4 ,11 ]
Brichant, Jean Francois [6 ]
Maquet, Pierre [4 ,7 ]
Laureys, Steven [2 ,3 ,4 ,7 ]
机构
[1] CHR Citadelle, Univ Dept Anesthesia & Intens Care Med, Bd 12eme Ligne 1, B-4000 Liege, Belgium
[2] CHU Univ Hosp Liege, Liege, Belgium
[3] Univ Liege, Coma Sci Grp, GIGA Res, Liege, Belgium
[4] Univ Liege, GIGA Cyclotron Res Ctr Vivo Imaging, Liege, Belgium
[5] CHU Univ Hosp Liege, Dept Algol & Palliat Care, Liege, Belgium
[6] CHU Univ Hosp Liege, Dept Anesthesia & Intens Care Med, Liege, Belgium
[7] CHU Univ Hosp Liege, Dept Neurol, Liege, Belgium
[8] Univ Wisconsin, Dept Neurol, Madison, WI 53706 USA
[9] Univ Western Ontario, Dept Anesthesia, London, ON, Canada
[10] Univ Western Ontario, Dept Intens Care Med, London, ON, Canada
[11] Univ Western Ontario, Dept Phys & Astron, London, ON, Canada
[12] Hop La Pitie Salpetriere, Inst Cerveau & Moelle Epiniere ICM, Paris, France
关键词
PROPOFOL-INDUCED LOSS; GENERAL-ANESTHESIA; HUMAN BRAIN; SEDATION; DISRUPTION;
D O I
10.1097/ALN.0000000000001275
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Consciousness-altering anesthetic agents disturb connectivity between brain regions composing the resting-state consciousness networks (RSNs). The default mode network (DMn), executive control network, salience network (SALn), auditory network, sensorimotor network (SMn), and visual network sustain mentation. Ketamine modifies consciousness differently from other agents, producing psychedelic dreaming and no apparent interaction with the environment. The authors used functional magnetic resonance imaging to explore ketamine-induced changes in RSNs connectivity. Methods: Fourteen healthy volunteers received stepwise intravenous infusions of ketamine up to loss of responsiveness. Because of agitation, data from six subjects were excluded from analysis. RSNs connectivity was compared between absence of ketamine (wake state [W1]), light ketamine sedation, and ketamine-induced unresponsiveness (deep sedation [S2]). Results: Increasing the depth of ketamine sedation from W1 to S2 altered DMn and SALn connectivity and suppressed the anticorrelated activity between DMn and other brain regions. During S2, DMn connectivity, particularly between the medial prefrontal cortex and the remaining network (effect size beta [95% CI]: W1 = 0.20 [0.18 to 0.22]; S2 = 0.07 [0.04 to 0.09]), and DMn anticorrelated activity (e.g., right sensory cortex: W1 = -0.07 [-0.09 to -0.04]; S2 = 0.04 [0.01 to 0.06]) were broken down. SALn connectivity was nonuniformly suppressed (e.g., left parietal operculum: W1 = 0.08 [0.06 to 0.09]; S2 = 0.05 [0.02 to 0.07]). Executive control networks, auditory network, SMn, and visual network were minimally affected. Conclusions: Ketamine induces specific changes in connectivity within and between RSNs. Breakdown of frontoparietal DMn connectivity and DMn anticorrelation and sensory and SMn connectivity preservation are common to ketamine and propofol-induced alterations of consciousness.
引用
收藏
页码:873 / 888
页数:16
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