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  3. Leptomeningeal collaterals regulate reperfusion in ischemic stroke and rescue the brain from futile recanalization.
 

Leptomeningeal collaterals regulate reperfusion in ischemic stroke and rescue the brain from futile recanalization.

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BORIS DOI
10.48350/193536
Date of Publication
May 1, 2024
Publication Type
Article
Division/Institute

ARTORG Center for Bio...

Contributor
Binder, Nadine Felizitas
El Amki, Mohamad
Glück, Chaim
Middleham, William
Reuss, Anna Maria
Bertolo, Adrien
Thurner, Patrick
Deffieux, Thomas
Lambride, Chryso
ARTORG Center for Biomedical Engineering Research
Epp, Robert
Handelsmann, Hannah-Lea
Baumgartner, Philipp
Orset, Cyrille
Bethge, Philipp
Kulcsar, Zsolt
Aguzzi, Adriano
Tanter, Mickael
Schmid, Franca
Vivien, Denis
Wyss, Matthias Tasso
Luft, Andreas
Weller, Michael
Weber, Bruno
Wegener, Susanne
Subject(s)

500 - Science::570 - ...

600 - Technology::610...

Series
Neuron
ISSN or ISBN (if monograph)
1097-4199
Publisher
Elsevier
Language
English
Publisher DOI
10.1016/j.neuron.2024.01.031
PubMed ID
38412858
Uncontrolled Keywords

in vivo imaging ische...

Description
Recanalization is the mainstay of ischemic stroke treatment. However, even with timely clot removal, many stroke patients recover poorly. Leptomeningeal collaterals (LMCs) are pial anastomotic vessels with yet-unknown functions. We applied laser speckle imaging, ultrafast ultrasound, and two-photon microscopy in a thrombin-based mouse model of stroke and fibrinolytic treatment to show that LMCs maintain cerebral autoregulation and allow for gradual reperfusion, resulting in small infarcts. In mice with poor LMCs, distal arterial segments collapse, and deleterious hyperemia causes hemorrhage and mortality after recanalization. In silico analyses confirm the relevance of LMCs for preserving perfusion in the ischemic region. Accordingly, in stroke patients with poor collaterals undergoing thrombectomy, rapid reperfusion resulted in hemorrhagic transformation and unfavorable recovery. Thus, we identify LMCs as key components regulating reperfusion and preventing futile recanalization after stroke. Future therapeutic interventions should aim to enhance collateral function, allowing for beneficial reperfusion after stroke.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/174967
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1-s2.0-S0896627324000576-main.pdftextAdobe PDF10.49 MBpublishedOpen
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