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Cerebrospinal fluid sodium rhythms

BACKGROUND: Cerebrospinal fluid (CSF) sodium levels have been reported to rise during episodic migraine. Since migraine frequently starts in early morning or late afternoon, we hypothesized that natural sodium chronobiology may predispose susceptible persons when extracellular CSF sodium increases....

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Autores principales: Harrington, Michael G, Salomon, Ronald M, Pogoda, Janice M, Oborina, Elena, Okey, Neil, Johnson, Benjamin, Schmidt, Dennis, Fonteh, Alfred N, Dalleska, Nathan F
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2822736/
https://www.ncbi.nlm.nih.gov/pubmed/20205754
http://dx.doi.org/10.1186/1743-8454-7-3
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author Harrington, Michael G
Salomon, Ronald M
Pogoda, Janice M
Oborina, Elena
Okey, Neil
Johnson, Benjamin
Schmidt, Dennis
Fonteh, Alfred N
Dalleska, Nathan F
author_facet Harrington, Michael G
Salomon, Ronald M
Pogoda, Janice M
Oborina, Elena
Okey, Neil
Johnson, Benjamin
Schmidt, Dennis
Fonteh, Alfred N
Dalleska, Nathan F
author_sort Harrington, Michael G
collection PubMed
description BACKGROUND: Cerebrospinal fluid (CSF) sodium levels have been reported to rise during episodic migraine. Since migraine frequently starts in early morning or late afternoon, we hypothesized that natural sodium chronobiology may predispose susceptible persons when extracellular CSF sodium increases. Since no mammalian brain sodium rhythms are known, we designed a study of healthy humans to test if cation rhythms exist in CSF. METHODS: Lumbar CSF was collected every ten minutes at 0.1 mL/min for 24 h from six healthy participants. CSF sodium and potassium concentrations were measured by ion chromatography, total protein by fluorescent spectrometry, and osmolarity by freezing point depression. We analyzed cation and protein distributions over the 24 h period and spectral and permutation tests to identify significant rhythms. We applied the False Discovery Rate method to adjust significance levels for multiple tests and Spearman correlations to compare sodium fluctuations with potassium, protein, and osmolarity. RESULTS: The distribution of sodium varied much more than potassium, and there were statistically significant rhythms at 12 and 1.65 h periods. Curve fitting to the average time course of the mean sodium of all six subjects revealed the lowest sodium levels at 03.20 h and highest at 08.00 h, a second nadir at 09.50 h and a second peak at 18.10 h. Sodium levels were not correlated with potassium or protein concentration, or with osmolarity. CONCLUSION: These CSF rhythms are the first reports of sodium chronobiology in the human nervous system. The results are consistent with our hypothesis that rising levels of extracellular sodium may contribute to the timing of migraine onset. The physiological importance of sodium in the nervous system suggests that these rhythms may have additional repercussions on ultradian functions.
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spelling pubmed-28227362010-02-17 Cerebrospinal fluid sodium rhythms Harrington, Michael G Salomon, Ronald M Pogoda, Janice M Oborina, Elena Okey, Neil Johnson, Benjamin Schmidt, Dennis Fonteh, Alfred N Dalleska, Nathan F Cerebrospinal Fluid Res Research BACKGROUND: Cerebrospinal fluid (CSF) sodium levels have been reported to rise during episodic migraine. Since migraine frequently starts in early morning or late afternoon, we hypothesized that natural sodium chronobiology may predispose susceptible persons when extracellular CSF sodium increases. Since no mammalian brain sodium rhythms are known, we designed a study of healthy humans to test if cation rhythms exist in CSF. METHODS: Lumbar CSF was collected every ten minutes at 0.1 mL/min for 24 h from six healthy participants. CSF sodium and potassium concentrations were measured by ion chromatography, total protein by fluorescent spectrometry, and osmolarity by freezing point depression. We analyzed cation and protein distributions over the 24 h period and spectral and permutation tests to identify significant rhythms. We applied the False Discovery Rate method to adjust significance levels for multiple tests and Spearman correlations to compare sodium fluctuations with potassium, protein, and osmolarity. RESULTS: The distribution of sodium varied much more than potassium, and there were statistically significant rhythms at 12 and 1.65 h periods. Curve fitting to the average time course of the mean sodium of all six subjects revealed the lowest sodium levels at 03.20 h and highest at 08.00 h, a second nadir at 09.50 h and a second peak at 18.10 h. Sodium levels were not correlated with potassium or protein concentration, or with osmolarity. CONCLUSION: These CSF rhythms are the first reports of sodium chronobiology in the human nervous system. The results are consistent with our hypothesis that rising levels of extracellular sodium may contribute to the timing of migraine onset. The physiological importance of sodium in the nervous system suggests that these rhythms may have additional repercussions on ultradian functions. BioMed Central 2010-01-20 /pmc/articles/PMC2822736/ /pubmed/20205754 http://dx.doi.org/10.1186/1743-8454-7-3 Text en Copyright ©2010 Harrington et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Harrington, Michael G
Salomon, Ronald M
Pogoda, Janice M
Oborina, Elena
Okey, Neil
Johnson, Benjamin
Schmidt, Dennis
Fonteh, Alfred N
Dalleska, Nathan F
Cerebrospinal fluid sodium rhythms
title Cerebrospinal fluid sodium rhythms
title_full Cerebrospinal fluid sodium rhythms
title_fullStr Cerebrospinal fluid sodium rhythms
title_full_unstemmed Cerebrospinal fluid sodium rhythms
title_short Cerebrospinal fluid sodium rhythms
title_sort cerebrospinal fluid sodium rhythms
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2822736/
https://www.ncbi.nlm.nih.gov/pubmed/20205754
http://dx.doi.org/10.1186/1743-8454-7-3
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