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Brain vulnerability and viability after ischaemia.
Daniele, Stefano G; Trummer, Georg; Hossmann, Konstantin A; Vrselja, Zvonimir; Benk, Christoph; Gobeske, Kevin T; Damjanovic, Domagoj; Andrijevic, David; Pooth, Jan-Steffen; Dellal, David; Beyersdorf, Friedhelm; Sestan, Nenad.
Afiliação
  • Daniele SG; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Trummer G; Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Hossmann KA; Medical Scientist Training Program (MD-PhD), Yale School of Medicine, New Haven, CT, USA.
  • Vrselja Z; Department of Cardiovascular Surgery, University Hospital Freiburg, Medical Faculty of the Albert-Ludwigs-University Freiburg, Freiburg, Germany.
  • Benk C; Max Planck Institute for Metabolism Research, Cologne, Germany.
  • Gobeske KT; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Damjanovic D; Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Andrijevic D; Department of Cardiovascular Surgery, University Hospital Freiburg, Medical Faculty of the Albert-Ludwigs-University Freiburg, Freiburg, Germany.
  • Pooth JS; Division of Neurocritical Care and Emergency Neurology, Department of Neurology, Yale School of Medicine, New Haven, CT, USA.
  • Dellal D; Department of Cardiovascular Surgery, University Hospital Freiburg, Medical Faculty of the Albert-Ludwigs-University Freiburg, Freiburg, Germany.
  • Beyersdorf F; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Sestan N; Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT, USA.
Nat Rev Neurosci ; 22(9): 553-572, 2021 09.
Article em En | MEDLINE | ID: mdl-34290397
ABSTRACT
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Isquemia Encefálica / Circulação Cerebrovascular / Neuroproteção Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Isquemia Encefálica / Circulação Cerebrovascular / Neuroproteção Idioma: En Ano de publicação: 2021 Tipo de documento: Article