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Nocturnal increase in cerebrospinal fluid secretion as a circadian regulator of intracranial pressure
BACKGROUND: It is crucial to maintain the intracranial pressure (ICP) within the physiological range to ensure proper brain function. The ICP may fluctuate during the light-dark phase cycle, complicating diagnosis and treatment choice in patients with pressure-related disorders. Such ICP fluctuation...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290349/ https://www.ncbi.nlm.nih.gov/pubmed/37353833 http://dx.doi.org/10.1186/s12987-023-00451-2 |
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author | Steffensen, Annette Buur Edelbo, Beatriche Louise Barbuskaite, Dagne Andreassen, Søren Norge Olsen, Markus Harboe Møller, Kirsten MacAulay, Nanna |
author_facet | Steffensen, Annette Buur Edelbo, Beatriche Louise Barbuskaite, Dagne Andreassen, Søren Norge Olsen, Markus Harboe Møller, Kirsten MacAulay, Nanna |
author_sort | Steffensen, Annette Buur |
collection | PubMed |
description | BACKGROUND: It is crucial to maintain the intracranial pressure (ICP) within the physiological range to ensure proper brain function. The ICP may fluctuate during the light-dark phase cycle, complicating diagnosis and treatment choice in patients with pressure-related disorders. Such ICP fluctuations may originate in circadian or sleep-wake cycle-mediated modulation of cerebrospinal fluid (CSF) flow dynamics, which in addition could support diurnal regulation of brain waste clearance. METHODS: ICP was monitored continuously in patients who underwent placement of an external ventricular drain (EVD) and by telemetric monitoring in experimental rats. CSF was collected via the EVD in patients and the rodent CSF secretion rate determined by in vivo experimentation. Rodent choroid plexus transporter transcripts were quantified with RNAseq and transport activity with ex vivo isotope transport assays. RESULTS: We demonstrated that ICP increases by 30% in the dark phase in both species, independently of vascular parameters. This increase aligns with elevated CSF collection in patients (12%) and CSF production rate in rats (20%), the latter obtained with the ventriculo-cisternal perfusion assay. The dark-phase increase in CSF secretion in rats was, in part, assigned to increased transport activity of the choroid plexus Na(+),K(+),2Cl(-) cotransporter (NKCC1), which is implicated in CSF secretion by this tissue. CONCLUSION: CSF secretion, and thus ICP, increases in the dark phase in humans and rats, irrespective of their diurnal/nocturnal activity preference, in part due to altered choroid plexus transport activity in the rat. Our findings suggest that CSF dynamics are modulated by the circadian rhythm, rather than merely sleep itself. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12987-023-00451-2. |
format | Online Article Text |
id | pubmed-10290349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102903492023-06-25 Nocturnal increase in cerebrospinal fluid secretion as a circadian regulator of intracranial pressure Steffensen, Annette Buur Edelbo, Beatriche Louise Barbuskaite, Dagne Andreassen, Søren Norge Olsen, Markus Harboe Møller, Kirsten MacAulay, Nanna Fluids Barriers CNS Research BACKGROUND: It is crucial to maintain the intracranial pressure (ICP) within the physiological range to ensure proper brain function. The ICP may fluctuate during the light-dark phase cycle, complicating diagnosis and treatment choice in patients with pressure-related disorders. Such ICP fluctuations may originate in circadian or sleep-wake cycle-mediated modulation of cerebrospinal fluid (CSF) flow dynamics, which in addition could support diurnal regulation of brain waste clearance. METHODS: ICP was monitored continuously in patients who underwent placement of an external ventricular drain (EVD) and by telemetric monitoring in experimental rats. CSF was collected via the EVD in patients and the rodent CSF secretion rate determined by in vivo experimentation. Rodent choroid plexus transporter transcripts were quantified with RNAseq and transport activity with ex vivo isotope transport assays. RESULTS: We demonstrated that ICP increases by 30% in the dark phase in both species, independently of vascular parameters. This increase aligns with elevated CSF collection in patients (12%) and CSF production rate in rats (20%), the latter obtained with the ventriculo-cisternal perfusion assay. The dark-phase increase in CSF secretion in rats was, in part, assigned to increased transport activity of the choroid plexus Na(+),K(+),2Cl(-) cotransporter (NKCC1), which is implicated in CSF secretion by this tissue. CONCLUSION: CSF secretion, and thus ICP, increases in the dark phase in humans and rats, irrespective of their diurnal/nocturnal activity preference, in part due to altered choroid plexus transport activity in the rat. Our findings suggest that CSF dynamics are modulated by the circadian rhythm, rather than merely sleep itself. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12987-023-00451-2. BioMed Central 2023-06-23 /pmc/articles/PMC10290349/ /pubmed/37353833 http://dx.doi.org/10.1186/s12987-023-00451-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Steffensen, Annette Buur Edelbo, Beatriche Louise Barbuskaite, Dagne Andreassen, Søren Norge Olsen, Markus Harboe Møller, Kirsten MacAulay, Nanna Nocturnal increase in cerebrospinal fluid secretion as a circadian regulator of intracranial pressure |
title | Nocturnal increase in cerebrospinal fluid secretion as a circadian regulator of intracranial pressure |
title_full | Nocturnal increase in cerebrospinal fluid secretion as a circadian regulator of intracranial pressure |
title_fullStr | Nocturnal increase in cerebrospinal fluid secretion as a circadian regulator of intracranial pressure |
title_full_unstemmed | Nocturnal increase in cerebrospinal fluid secretion as a circadian regulator of intracranial pressure |
title_short | Nocturnal increase in cerebrospinal fluid secretion as a circadian regulator of intracranial pressure |
title_sort | nocturnal increase in cerebrospinal fluid secretion as a circadian regulator of intracranial pressure |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290349/ https://www.ncbi.nlm.nih.gov/pubmed/37353833 http://dx.doi.org/10.1186/s12987-023-00451-2 |
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