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Precapillary sphincters maintain perfusion in the cerebral cortex

Active nerve cells release vasodilators that increase their energy supply by dilating local blood vessels, a mechanism termed neurovascular coupling and the basis of BOLD functional neuroimaging signals. Here, we reveal a mechanism for cerebral blood flow control, a precapillary sphincter at the tra...

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Autores principales: Grubb, Søren, Cai, Changsi, Hald, Bjørn O., Khennouf, Lila, Murmu, Reena Prity, Jensen, Aske G. K., Fordsmann, Jonas, Zambach, Stefan, Lauritzen, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971292/
https://www.ncbi.nlm.nih.gov/pubmed/31959752
http://dx.doi.org/10.1038/s41467-020-14330-z
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author Grubb, Søren
Cai, Changsi
Hald, Bjørn O.
Khennouf, Lila
Murmu, Reena Prity
Jensen, Aske G. K.
Fordsmann, Jonas
Zambach, Stefan
Lauritzen, Martin
author_facet Grubb, Søren
Cai, Changsi
Hald, Bjørn O.
Khennouf, Lila
Murmu, Reena Prity
Jensen, Aske G. K.
Fordsmann, Jonas
Zambach, Stefan
Lauritzen, Martin
author_sort Grubb, Søren
collection PubMed
description Active nerve cells release vasodilators that increase their energy supply by dilating local blood vessels, a mechanism termed neurovascular coupling and the basis of BOLD functional neuroimaging signals. Here, we reveal a mechanism for cerebral blood flow control, a precapillary sphincter at the transition between the penetrating arteriole and first order capillary, linking blood flow in capillaries to the arteriolar inflow. The sphincters are encircled by contractile mural cells, which are capable of bidirectional control of the length and width of the enclosed vessel segment. The hemodynamic consequence is that precapillary sphincters can generate the largest changes in the cerebrovascular flow resistance of all brain vessel segments, thereby controlling capillary flow while protecting the downstream capillary bed and brain tissue from adverse pressure fluctuations. Cortical spreading depolarization constricts sphincters and causes vascular trapping of blood cells. Thus, precapillary sphincters are bottlenecks for brain capillary blood flow.
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spelling pubmed-69712922020-01-22 Precapillary sphincters maintain perfusion in the cerebral cortex Grubb, Søren Cai, Changsi Hald, Bjørn O. Khennouf, Lila Murmu, Reena Prity Jensen, Aske G. K. Fordsmann, Jonas Zambach, Stefan Lauritzen, Martin Nat Commun Article Active nerve cells release vasodilators that increase their energy supply by dilating local blood vessels, a mechanism termed neurovascular coupling and the basis of BOLD functional neuroimaging signals. Here, we reveal a mechanism for cerebral blood flow control, a precapillary sphincter at the transition between the penetrating arteriole and first order capillary, linking blood flow in capillaries to the arteriolar inflow. The sphincters are encircled by contractile mural cells, which are capable of bidirectional control of the length and width of the enclosed vessel segment. The hemodynamic consequence is that precapillary sphincters can generate the largest changes in the cerebrovascular flow resistance of all brain vessel segments, thereby controlling capillary flow while protecting the downstream capillary bed and brain tissue from adverse pressure fluctuations. Cortical spreading depolarization constricts sphincters and causes vascular trapping of blood cells. Thus, precapillary sphincters are bottlenecks for brain capillary blood flow. Nature Publishing Group UK 2020-01-20 /pmc/articles/PMC6971292/ /pubmed/31959752 http://dx.doi.org/10.1038/s41467-020-14330-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Grubb, Søren
Cai, Changsi
Hald, Bjørn O.
Khennouf, Lila
Murmu, Reena Prity
Jensen, Aske G. K.
Fordsmann, Jonas
Zambach, Stefan
Lauritzen, Martin
Precapillary sphincters maintain perfusion in the cerebral cortex
title Precapillary sphincters maintain perfusion in the cerebral cortex
title_full Precapillary sphincters maintain perfusion in the cerebral cortex
title_fullStr Precapillary sphincters maintain perfusion in the cerebral cortex
title_full_unstemmed Precapillary sphincters maintain perfusion in the cerebral cortex
title_short Precapillary sphincters maintain perfusion in the cerebral cortex
title_sort precapillary sphincters maintain perfusion in the cerebral cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971292/
https://www.ncbi.nlm.nih.gov/pubmed/31959752
http://dx.doi.org/10.1038/s41467-020-14330-z
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