Role of the Gut Microbiome in Obstructive Sleep Apnea-Induced Hypertension
Individuals suffering from obstructive sleep apnea (OSA) are at increased risk for systemic hypertension. The importance of a healthy gut microbiota, and detriment of a dysbiotic microbiota, on host physiology is becoming increasingly evident. We tested the hypothesis that gut dysbiosis contributes...
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Veröffentlicht in: | Hypertension (Dallas, Tex. 1979) Tex. 1979), 2016-02, Vol.67 (2), p.469-474 |
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creator | Durgan, David J Ganesh, Bhanu P Cope, Julia L Ajami, Nadim J Phillips, Sharon C Petrosino, Joseph F Hollister, Emily B Bryan, Jr, Robert M |
description | Individuals suffering from obstructive sleep apnea (OSA) are at increased risk for systemic hypertension. The importance of a healthy gut microbiota, and detriment of a dysbiotic microbiota, on host physiology is becoming increasingly evident. We tested the hypothesis that gut dysbiosis contributes to hypertension observed with OSA. OSA was modeled in rats by inflating a tracheal balloon during the sleep cycle (10-s inflations, 60 per hour). On normal chow diet, OSA had no effect on blood pressure; however, in rats fed a high-fat diet, blood pressure increased 24 and 29 mm Hg after 7 and 14 days of OSA, respectively (P |
doi_str_mv | 10.1161/HYPERTENSIONAHA.115.06672 |
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The importance of a healthy gut microbiota, and detriment of a dysbiotic microbiota, on host physiology is becoming increasingly evident. We tested the hypothesis that gut dysbiosis contributes to hypertension observed with OSA. OSA was modeled in rats by inflating a tracheal balloon during the sleep cycle (10-s inflations, 60 per hour). On normal chow diet, OSA had no effect on blood pressure; however, in rats fed a high-fat diet, blood pressure increased 24 and 29 mm Hg after 7 and 14 days of OSA, respectively (P<0.05 each). Bacterial community characterization was performed on fecal pellets isolated before and after 14 days of OSA in chow and high-fat fed rats. High-fat diet and OSA led to significant alterations of the gut microbiota, including decreases in bacterial taxa known to produce the short chain fatty acid butyrate (P<0.05). Finally, transplant of dysbiotic cecal contents from hypertensive OSA rats on high-fat diet into OSA recipient rats on normal chow diet (shown to be normotensive) resulted in hypertension similar to that of the donor (increased 14 and 32 mm Hg after 7 and 14 days of OSA, respectively; P<0.05). These studies demonstrate a causal relationship between gut dysbiosis and hypertension, and suggest that manipulation of the microbiota may be a viable treatment for OSA-induced, and possibly other forms of, hypertension.</description><identifier>ISSN: 0194-911X</identifier><identifier>EISSN: 1524-4563</identifier><identifier>DOI: 10.1161/HYPERTENSIONAHA.115.06672</identifier><identifier>PMID: 26711739</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Blood Pressure - physiology ; Disease Models, Animal ; Dysbiosis - complications ; Dysbiosis - microbiology ; Gastrointestinal Microbiome - physiology ; Hypertension - etiology ; Hypertension - physiopathology ; Male ; Polysomnography ; Rats ; Rats, Long-Evans ; Sleep - physiology ; Sleep Apnea Syndromes - complications ; Sleep Apnea Syndromes - microbiology ; Sleep Apnea Syndromes - physiopathology</subject><ispartof>Hypertension (Dallas, Tex. 1979), 2016-02, Vol.67 (2), p.469-474</ispartof><rights>2015 American Heart Association, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c549t-e0a0eaa51b262a3abe90e3f49b7759c1938862adbdf48266cbd1942862f892903</citedby><cites>FETCH-LOGICAL-c549t-e0a0eaa51b262a3abe90e3f49b7759c1938862adbdf48266cbd1942862f892903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3674,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26711739$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Durgan, David J</creatorcontrib><creatorcontrib>Ganesh, Bhanu P</creatorcontrib><creatorcontrib>Cope, Julia L</creatorcontrib><creatorcontrib>Ajami, Nadim J</creatorcontrib><creatorcontrib>Phillips, Sharon C</creatorcontrib><creatorcontrib>Petrosino, Joseph F</creatorcontrib><creatorcontrib>Hollister, Emily B</creatorcontrib><creatorcontrib>Bryan, Jr, Robert M</creatorcontrib><title>Role of the Gut Microbiome in Obstructive Sleep Apnea-Induced Hypertension</title><title>Hypertension (Dallas, Tex. 1979)</title><addtitle>Hypertension</addtitle><description>Individuals suffering from obstructive sleep apnea (OSA) are at increased risk for systemic hypertension. The importance of a healthy gut microbiota, and detriment of a dysbiotic microbiota, on host physiology is becoming increasingly evident. We tested the hypothesis that gut dysbiosis contributes to hypertension observed with OSA. OSA was modeled in rats by inflating a tracheal balloon during the sleep cycle (10-s inflations, 60 per hour). On normal chow diet, OSA had no effect on blood pressure; however, in rats fed a high-fat diet, blood pressure increased 24 and 29 mm Hg after 7 and 14 days of OSA, respectively (P<0.05 each). Bacterial community characterization was performed on fecal pellets isolated before and after 14 days of OSA in chow and high-fat fed rats. High-fat diet and OSA led to significant alterations of the gut microbiota, including decreases in bacterial taxa known to produce the short chain fatty acid butyrate (P<0.05). Finally, transplant of dysbiotic cecal contents from hypertensive OSA rats on high-fat diet into OSA recipient rats on normal chow diet (shown to be normotensive) resulted in hypertension similar to that of the donor (increased 14 and 32 mm Hg after 7 and 14 days of OSA, respectively; P<0.05). These studies demonstrate a causal relationship between gut dysbiosis and hypertension, and suggest that manipulation of the microbiota may be a viable treatment for OSA-induced, and possibly other forms of, hypertension.</description><subject>Animals</subject><subject>Blood Pressure - physiology</subject><subject>Disease Models, Animal</subject><subject>Dysbiosis - complications</subject><subject>Dysbiosis - microbiology</subject><subject>Gastrointestinal Microbiome - physiology</subject><subject>Hypertension - etiology</subject><subject>Hypertension - physiopathology</subject><subject>Male</subject><subject>Polysomnography</subject><subject>Rats</subject><subject>Rats, Long-Evans</subject><subject>Sleep - physiology</subject><subject>Sleep Apnea Syndromes - complications</subject><subject>Sleep Apnea Syndromes - microbiology</subject><subject>Sleep Apnea Syndromes - physiopathology</subject><issn>0194-911X</issn><issn>1524-4563</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdUctO3DAUtVBRmdL-QuXuugn4xq94U2mEpswgYCoeEqwsJ7kpRpk4xAkSf49bHgJWVzr3nHMfh5AfwPYAFOwvr_8szi4Wp-er9el8OU-g3GNK6XyLzEDmIhNS8U9kxsCIzABc7ZAvMd4yBkII_Zns5EoDaG5m5OgstEhDQ8cbpIfTSE98NYTShw1S39F1GcdhqkZ_j_S8RezpvO_QZauuniqs6fKhx2HELvrQfSXbjWsjfnuuu-Ty9-LiYJkdrw9XB_PjrJLCjBkyx9A5CWWucsddiYYhb4QptZamAsOLIjXqsm5EkStVlXU6I09YU5jcML5Lfj359lO5wbrCbhxca_vBb9zwYIPz9n2n8zf2b7i3QgPnyiSDn88GQ7ibMI5242OFbes6DFO0oBUrtJRQJKp5oqanxDhg8zoGmP2Xhf2QRQKl_Z9F0n5_u-er8uX5_BEaOohP</recordid><startdate>20160201</startdate><enddate>20160201</enddate><creator>Durgan, David J</creator><creator>Ganesh, Bhanu P</creator><creator>Cope, Julia L</creator><creator>Ajami, Nadim J</creator><creator>Phillips, Sharon C</creator><creator>Petrosino, Joseph F</creator><creator>Hollister, Emily B</creator><creator>Bryan, Jr, Robert M</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160201</creationdate><title>Role of the Gut Microbiome in Obstructive Sleep Apnea-Induced Hypertension</title><author>Durgan, David J ; 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Finally, transplant of dysbiotic cecal contents from hypertensive OSA rats on high-fat diet into OSA recipient rats on normal chow diet (shown to be normotensive) resulted in hypertension similar to that of the donor (increased 14 and 32 mm Hg after 7 and 14 days of OSA, respectively; P<0.05). These studies demonstrate a causal relationship between gut dysbiosis and hypertension, and suggest that manipulation of the microbiota may be a viable treatment for OSA-induced, and possibly other forms of, hypertension.</abstract><cop>United States</cop><pmid>26711739</pmid><doi>10.1161/HYPERTENSIONAHA.115.06672</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Blood Pressure - physiology Disease Models, Animal Dysbiosis - complications Dysbiosis - microbiology Gastrointestinal Microbiome - physiology Hypertension - etiology Hypertension - physiopathology Male Polysomnography Rats Rats, Long-Evans Sleep - physiology Sleep Apnea Syndromes - complications Sleep Apnea Syndromes - microbiology Sleep Apnea Syndromes - physiopathology |
title | Role of the Gut Microbiome in Obstructive Sleep Apnea-Induced Hypertension |
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