Brain vulnerability and viability after ischaemia.


Journal

Nature reviews. Neuroscience
ISSN: 1471-0048
Titre abrégé: Nat Rev Neurosci
Pays: England
ID NLM: 100962781

Informations de publication

Date de publication:
09 2021
Historique:
accepted: 14 06 2021
pubmed: 23 7 2021
medline: 28 9 2021
entrez: 22 7 2021
Statut: ppublish

Résumé

The susceptibility of the brain to ischaemic injury dramatically limits its viability following interruptions in blood flow. However, data from studies of dissociated cells, tissue specimens, isolated organs and whole bodies have brought into question the temporal limits within which the brain is capable of tolerating prolonged circulatory arrest. This Review assesses cell type-specific mechanisms of global cerebral ischaemia, and examines the circumstances in which the brain exhibits heightened resilience to injury. We suggest strategies for expanding such discoveries to fuel translational research into novel cytoprotective therapies, and describe emerging technologies and experimental concepts. By doing so, we propose a new multimodal framework to investigate brain resuscitation following extended periods of circulatory arrest.

Identifiants

pubmed: 34290397
doi: 10.1038/s41583-021-00488-y
pii: 10.1038/s41583-021-00488-y
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

553-572

Informations de copyright

© 2021. Springer Nature Limited.

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Auteurs

Stefano G Daniele (SG)

Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT, USA.
Medical Scientist Training Program (MD-PhD), Yale School of Medicine, New Haven, CT, USA.

Georg Trummer (G)

Department of Cardiovascular Surgery, University Hospital Freiburg, Medical Faculty of the Albert-Ludwigs-University Freiburg, Freiburg, Germany.

Konstantin A Hossmann (KA)

Max Planck Institute for Metabolism Research, Cologne, Germany.

Zvonimir Vrselja (Z)

Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT, USA.

Christoph Benk (C)

Department of Cardiovascular Surgery, University Hospital Freiburg, Medical Faculty of the Albert-Ludwigs-University Freiburg, Freiburg, Germany.

Kevin T Gobeske (KT)

Division of Neurocritical Care and Emergency Neurology, Department of Neurology, Yale School of Medicine, New Haven, CT, USA.

Domagoj Damjanovic (D)

Department of Cardiovascular Surgery, University Hospital Freiburg, Medical Faculty of the Albert-Ludwigs-University Freiburg, Freiburg, Germany.

David Andrijevic (D)

Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT, USA.

Jan-Steffen Pooth (JS)

Department of Cardiovascular Surgery, University Hospital Freiburg, Medical Faculty of the Albert-Ludwigs-University Freiburg, Freiburg, Germany.

David Dellal (D)

Department of Biomedical Engineering, Yale University, New Haven, CT, USA.

Friedhelm Beyersdorf (F)

Department of Cardiovascular Surgery, University Hospital Freiburg, Medical Faculty of the Albert-Ludwigs-University Freiburg, Freiburg, Germany. friedhelm.beyersdorf@uniklinik-freiburg.de.

Nenad Sestan (N)

Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA. nenad.sestan@yale.edu.
Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT, USA. nenad.sestan@yale.edu.
Department of Genetics, Yale School of Medicine, New Haven, CT, USA. nenad.sestan@yale.edu.
Department of Psychiatry, Yale School of Medicine, New Haven, CT, USA. nenad.sestan@yale.edu.
Department of Comparative Medicine, Yale School of Medicine, New Haven, CT, USA. nenad.sestan@yale.edu.
Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale School of Medicine, New Haven, CT, USA. nenad.sestan@yale.edu.
Yale Child Study Center, New Haven, CT, USA. nenad.sestan@yale.edu.

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