Cargando…

Sleep fragmentation increases blood pressure and is associated with alterations in the gut microbiome and fecal metabolome in rats

The gut microbiota, via the production of metabolites entering the circulation, plays a role in blood pressure regulation. Blood pressure is also affected by the characteristics of sleep. To date, no studies have examined relationships among the gut microbiota/metabolites, blood pressure, and sleep....

Descripción completa

Detalles Bibliográficos
Autores principales: Maki, Katherine A., Burke, Larisa A., Calik, Michael W., Watanabe-Chailland, Miki, Sweeney, Dagmar, Romick-Rosendale, Lindsey E., Green, Stefan J., Fink, Anne M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Physiological Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468692/
https://www.ncbi.nlm.nih.gov/pubmed/32567509
http://dx.doi.org/10.1152/physiolgenomics.00039.2020
_version_ 1783578273664466944
author Maki, Katherine A.
Burke, Larisa A.
Calik, Michael W.
Watanabe-Chailland, Miki
Sweeney, Dagmar
Romick-Rosendale, Lindsey E.
Green, Stefan J.
Fink, Anne M.
author_facet Maki, Katherine A.
Burke, Larisa A.
Calik, Michael W.
Watanabe-Chailland, Miki
Sweeney, Dagmar
Romick-Rosendale, Lindsey E.
Green, Stefan J.
Fink, Anne M.
author_sort Maki, Katherine A.
collection PubMed
description The gut microbiota, via the production of metabolites entering the circulation, plays a role in blood pressure regulation. Blood pressure is also affected by the characteristics of sleep. To date, no studies have examined relationships among the gut microbiota/metabolites, blood pressure, and sleep. We hypothesized that fragmented sleep is associated with elevated mean arterial pressure, an altered and dysbiotic gut microbial community, and changes in fecal metabolites. In our model system, rats were randomized to 8 h of sleep fragmentation during the rest phase (light phase) or were undisturbed (controls) for 28 consecutive days. Rats underwent sleep and blood pressure recordings, and fecal samples were analyzed during: baseline (days −4 to −1), early sleep fragmentation (days 0–3), midsleep fragmentation (days 6–13), late sleep fragmentation (days 20–27), and recovery/rest (days 28–34). Less sleep per hour during the sleep fragmentation period was associated with increased mean arterial pressure. Analyses of gut microbial communities and metabolites revealed that putative short chain fatty acid-producing bacteria were differentially abundant between control and intervention animals during mid-/late sleep fragmentation and recovery. Midsleep fragmentation was also characterized by lower alpha diversity, lower Firmicutes:Bacteroidetes ratio, and higher Proteobacteria in intervention rats. Elevated putative succinate-producing bacteria and acetate-producing bacteria were associated with lower and higher mean arterial pressure, respectively, and untargeted metabolomics analysis demonstrates that certain fecal metabolites are significantly correlated with blood pressure. These data reveal associations between sleep fragmentation, mean arterial pressure, and the gut microbiome/fecal metabolome and provide insight to links between disrupted sleep and cardiovascular pathology.
format Online
Article
Text
id pubmed-7468692
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Physiological Society
record_format MEDLINE/PubMed
spelling pubmed-74686922020-09-15 Sleep fragmentation increases blood pressure and is associated with alterations in the gut microbiome and fecal metabolome in rats Maki, Katherine A. Burke, Larisa A. Calik, Michael W. Watanabe-Chailland, Miki Sweeney, Dagmar Romick-Rosendale, Lindsey E. Green, Stefan J. Fink, Anne M. Physiol Genomics Research Article The gut microbiota, via the production of metabolites entering the circulation, plays a role in blood pressure regulation. Blood pressure is also affected by the characteristics of sleep. To date, no studies have examined relationships among the gut microbiota/metabolites, blood pressure, and sleep. We hypothesized that fragmented sleep is associated with elevated mean arterial pressure, an altered and dysbiotic gut microbial community, and changes in fecal metabolites. In our model system, rats were randomized to 8 h of sleep fragmentation during the rest phase (light phase) or were undisturbed (controls) for 28 consecutive days. Rats underwent sleep and blood pressure recordings, and fecal samples were analyzed during: baseline (days −4 to −1), early sleep fragmentation (days 0–3), midsleep fragmentation (days 6–13), late sleep fragmentation (days 20–27), and recovery/rest (days 28–34). Less sleep per hour during the sleep fragmentation period was associated with increased mean arterial pressure. Analyses of gut microbial communities and metabolites revealed that putative short chain fatty acid-producing bacteria were differentially abundant between control and intervention animals during mid-/late sleep fragmentation and recovery. Midsleep fragmentation was also characterized by lower alpha diversity, lower Firmicutes:Bacteroidetes ratio, and higher Proteobacteria in intervention rats. Elevated putative succinate-producing bacteria and acetate-producing bacteria were associated with lower and higher mean arterial pressure, respectively, and untargeted metabolomics analysis demonstrates that certain fecal metabolites are significantly correlated with blood pressure. These data reveal associations between sleep fragmentation, mean arterial pressure, and the gut microbiome/fecal metabolome and provide insight to links between disrupted sleep and cardiovascular pathology. American Physiological Society 2020-07-01 2020-06-22 /pmc/articles/PMC7468692/ /pubmed/32567509 http://dx.doi.org/10.1152/physiolgenomics.00039.2020 Text en Copyright © 2020 the American Physiological Society http://creativecommons.org/licenses/by/4.0/deed.en_US Licensed under Creative Commons Attribution CC-BY 4.0 (http://creativecommons.org/licenses/by/4.0/deed.en_US) : © the American Physiological Society.
spellingShingle Research Article
Maki, Katherine A.
Burke, Larisa A.
Calik, Michael W.
Watanabe-Chailland, Miki
Sweeney, Dagmar
Romick-Rosendale, Lindsey E.
Green, Stefan J.
Fink, Anne M.
Sleep fragmentation increases blood pressure and is associated with alterations in the gut microbiome and fecal metabolome in rats
title Sleep fragmentation increases blood pressure and is associated with alterations in the gut microbiome and fecal metabolome in rats
title_full Sleep fragmentation increases blood pressure and is associated with alterations in the gut microbiome and fecal metabolome in rats
title_fullStr Sleep fragmentation increases blood pressure and is associated with alterations in the gut microbiome and fecal metabolome in rats
title_full_unstemmed Sleep fragmentation increases blood pressure and is associated with alterations in the gut microbiome and fecal metabolome in rats
title_short Sleep fragmentation increases blood pressure and is associated with alterations in the gut microbiome and fecal metabolome in rats
title_sort sleep fragmentation increases blood pressure and is associated with alterations in the gut microbiome and fecal metabolome in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468692/
https://www.ncbi.nlm.nih.gov/pubmed/32567509
http://dx.doi.org/10.1152/physiolgenomics.00039.2020
work_keys_str_mv AT makikatherinea sleepfragmentationincreasesbloodpressureandisassociatedwithalterationsinthegutmicrobiomeandfecalmetabolomeinrats
AT burkelarisaa sleepfragmentationincreasesbloodpressureandisassociatedwithalterationsinthegutmicrobiomeandfecalmetabolomeinrats
AT calikmichaelw sleepfragmentationincreasesbloodpressureandisassociatedwithalterationsinthegutmicrobiomeandfecalmetabolomeinrats
AT watanabechaillandmiki sleepfragmentationincreasesbloodpressureandisassociatedwithalterationsinthegutmicrobiomeandfecalmetabolomeinrats
AT sweeneydagmar sleepfragmentationincreasesbloodpressureandisassociatedwithalterationsinthegutmicrobiomeandfecalmetabolomeinrats
AT romickrosendalelindseye sleepfragmentationincreasesbloodpressureandisassociatedwithalterationsinthegutmicrobiomeandfecalmetabolomeinrats
AT greenstefanj sleepfragmentationincreasesbloodpressureandisassociatedwithalterationsinthegutmicrobiomeandfecalmetabolomeinrats
AT finkannem sleepfragmentationincreasesbloodpressureandisassociatedwithalterationsinthegutmicrobiomeandfecalmetabolomeinrats