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Optogenetic stimulation of cholinergic brainstem neurons during focal limbic seizures: Effects on cortical physiology
Authors:Moran Furman  Qiong Zhan  Cian McCafferty  Benjamin A. Lerner  Joshua E. Motelow  Jin Meng  Chanthia Ma  Gordon F. Buchanan  Ilana B. Witten  Karl Deisseroth  Jessica A. Cardin  Hal Blumenfeld
Affiliation:1. Department of Neurology, Yale University School of Medicine, New Haven, Connecticut, U.S.A.;2. Xiangya Hospital, Central South University, Changsha, China;3. Psychology, Princeton University, Princeton, New Jersey, U.S.A.;4. Bioengineering, Psychiatry and Behavioral Science, Stanford University, Stanford, California, U.S.A.;5. Department of Neuroscience, Yale University School of Medicine, New Haven, Connecticut, U.S.A.;6. Kavli Institute, Yale University School of Medicine, New Haven, Connecticut, U.S.A.;7. Department of Neurosurgery, Yale University School of Medicine, New Haven, Connecticut, U.S.A.
Abstract:Focal temporal lobe seizures often cause impaired cortical function and loss of consciousness. Recent work suggests that the mechanism for depressed cortical function during focal seizures may depend on decreased subcortical cholinergic arousal, which leads to a sleep‐like state of cortical slow‐wave activity. To test this hypothesis, we sought to directly activate subcortical cholinergic neurons during focal limbic seizures to determine the effects on cortical function. Here we used an optogenetic approach to selectively stimulate cholinergic brainstem neurons in the pedunculopontine tegmental nucleus during focal limbic seizures induced in a lightly anesthetized rat model. We found an increase in cortical gamma activity and a decrease in delta activity in response to cholinergic stimulation. These findings support the mechanistic role of reduced subcortical cholinergic arousal in causing cortical dysfunction during seizures. Through further work, electrical or optogenetic stimulation of subcortical arousal networks may ultimately lead to new treatments aimed at preventing cortical dysfunction during seizures.
Keywords:Epilepsy  Consciousness  Optogenetics  Neurostimulation  Acetylcholine  Sudden unexpected death in epilepsy (SUDEP)
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