Spatial signatures of anesthesia-induced burst-suppression differ between primates and rodents.

macaque anesthesia burst-suppression common marmoset fMRI human isoflurane neuroscience rat sevoflurane

Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
24 05 2022
Historique:
received: 18 10 2021
accepted: 01 05 2022
entrez: 24 5 2022
pubmed: 25 5 2022
medline: 26 5 2022
Statut: epublish

Résumé

During deep anesthesia, the electroencephalographic (EEG) signal of the brain alternates between bursts of activity and periods of relative silence (suppressions). The origin of burst-suppression and its distribution across the brain remain matters of debate. In this work, we used functional magnetic resonance imaging (fMRI) to map the brain areas involved in anesthesia-induced burst-suppression across four mammalian species: humans, long-tailed macaques, common marmosets, and rats. At first, we determined the fMRI signatures of burst-suppression in human EEG-fMRI data. Applying this method to animal fMRI datasets, we found distinct burst-suppression signatures in all species. The burst-suppression maps revealed a marked inter-species difference: in rats, the entire neocortex engaged in burst-suppression, while in primates most sensory areas were excluded-predominantly the primary visual cortex. We anticipate that the identified species-specific fMRI signatures and whole-brain maps will guide future targeted studies investigating the cellular and molecular mechanisms of burst-suppression in unconscious states. The development of anesthesia was a significant advance in medicine. It allows individuals to undergo surgery without feeling pain or remembering the experience. But scientists still do not know how anesthesia works. During anesthesia, scientists have measured brain activity using electroencephalograms (EEG) and found that the brain appears to turn on and off. Comatose patients also have similar switches between bursts of electrical activity and periods of silence. This burst-suppression pattern may be related to unconsciousness. But scientists still have many questions about how anesthesia causes burst-suppression. One challenge is that while an EEG can tell scientists when the brain turns on and off, it does not show exactly where this occurs. Another imaging method called functional Magnetic Resonance Imaging (fMRI) may fill this gap by allowing scientists to map where the brain activity occurs. Sirmpilatze et al. have created detailed maps of burst-suppression in humans, primates, and rats under anesthesia by analyzing brain scans using fMRI. In rats, the entire outer layer or cortex of the brain underwent a synchronized pattern of burst-suppression. In humans and primates, areas of the brain like those responsible for eyesight did not follow the rest of the cortex in switching on and off. The experiments reveal crucial differences in how rats and humans and other primates respond to anesthesia. The fMRI mapping technique Sirmpilatze et al. created may help scientists learn more about these differences and why some parts of human brains do not undergo burst-suppression. This may help scientists learn more about unconsciousness and help improve anesthesia or the care of comatose patients.

Autres résumés

Type: plain-language-summary (eng)
The development of anesthesia was a significant advance in medicine. It allows individuals to undergo surgery without feeling pain or remembering the experience. But scientists still do not know how anesthesia works. During anesthesia, scientists have measured brain activity using electroencephalograms (EEG) and found that the brain appears to turn on and off. Comatose patients also have similar switches between bursts of electrical activity and periods of silence. This burst-suppression pattern may be related to unconsciousness. But scientists still have many questions about how anesthesia causes burst-suppression. One challenge is that while an EEG can tell scientists when the brain turns on and off, it does not show exactly where this occurs. Another imaging method called functional Magnetic Resonance Imaging (fMRI) may fill this gap by allowing scientists to map where the brain activity occurs. Sirmpilatze et al. have created detailed maps of burst-suppression in humans, primates, and rats under anesthesia by analyzing brain scans using fMRI. In rats, the entire outer layer or cortex of the brain underwent a synchronized pattern of burst-suppression. In humans and primates, areas of the brain like those responsible for eyesight did not follow the rest of the cortex in switching on and off. The experiments reveal crucial differences in how rats and humans and other primates respond to anesthesia. The fMRI mapping technique Sirmpilatze et al. created may help scientists learn more about these differences and why some parts of human brains do not undergo burst-suppression. This may help scientists learn more about unconsciousness and help improve anesthesia or the care of comatose patients.

Identifiants

pubmed: 35607889
doi: 10.7554/eLife.74813
pii: 74813
pmc: PMC9129882
doi:
pii:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2022, Sirmpilatze et al.

Déclaration de conflit d'intérêts

NS, JM, MO, JB, JP, DG, AR, RI, OG, SB No competing interests declared

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Auteurs

Nikoloz Sirmpilatze (N)

Functional Imaging Laboratory, German Primate Center - Leibniz Institute for Primate Research, Göttingen, Germany.
Georg-August University of Göttingen, Göttingen, Germany.
International Max Planck Research School for Neurosciences, Göttingen, Germany.

Judith Mylius (J)

Functional Imaging Laboratory, German Primate Center - Leibniz Institute for Primate Research, Göttingen, Germany.

Michael Ortiz-Rios (M)

Functional Imaging Laboratory, German Primate Center - Leibniz Institute for Primate Research, Göttingen, Germany.

Jürgen Baudewig (J)

Functional Imaging Laboratory, German Primate Center - Leibniz Institute for Primate Research, Göttingen, Germany.

Jaakko Paasonen (J)

A.I.V. Institute for Molecular Sciences, University of Eastern Finland, Kuopio, Finland.

Daniel Golkowski (D)

Department of Neurology, Klinikum Rechts der Isar der Technischen Universität München, Munich, Germany.
Department of Neurology, Heidelberg University Hospital, Heidelberg, Germany.

Andreas Ranft (A)

Department of Anesthesiology and Intensive Care Medicine, Klinikum Rechts der Isar der Technischen Universität München, Munich, Germany.

Rüdiger Ilg (R)

Department of Neurology, Klinikum Rechts der Isar der Technischen Universität München, Munich, Germany.
Department of Neurology, Asklepios Stadtklinik Bad Tölz, Bad Tölz, Germany.

Olli Gröhn (O)

A.I.V. Institute for Molecular Sciences, University of Eastern Finland, Kuopio, Finland.

Susann Boretius (S)

Functional Imaging Laboratory, German Primate Center - Leibniz Institute for Primate Research, Göttingen, Germany.
Georg-August University of Göttingen, Göttingen, Germany.
International Max Planck Research School for Neurosciences, Göttingen, Germany.
Leibniz Science Campus Primate Cognition, Göttingen, Germany.

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