Literature DB >> 35503026

Beyond the gastrointestinal tract: oral and sex-specific skin microbiota are associated with hypertension in rats with genetic disparities.

Xue Mei1, Blair Mell1, Xi Cheng1, Ji-Youn Yeo1, Tao Yang1, Nathaline Chiu1, Bina Joe1.   

Abstract

Current knowledge of the link between microbiota and hypertension is limited to the gut. Besides the gut, oral cavity and skin are other locations where sodium chloride (NaCl) is in direct contact with microbiota. Although oral nitrate-reducing bacteria generate nitric oxide, which leads to vasodilation and lowering of blood pressure (BP), the skin excretes sodium via sweat glands and is an important site for sodium and BP homeostasis. However, knowledge on the contributions of oral and skin microbiota to BP regulation, is limited. Therefore, the current study was conducted to compare the tripartite relationship between site, sex, and genetic effects on the composition of oral, skin, and gut microbiota impacting hypertension. Microbiota were profiled from the oral cavity, skin, and feces of both male and female hypertensive Dahl salt-sensitive (S) and congenic rats with genomic substitutions on rat chromosomes (RNO) 1, 5, 9, and 10, demonstrating disparate BP effects. Sex-specific differences in β-diversity were observed only in skin microbiota. The most abundant taxa of the oral and skin microbiota were Actinobacteria and Cyanobacteria, respectively. Oral Actinobacteria were inversely associated with BP. Although the abundance of oral Actinobacteria was upregulated by the BP locus on RNO10 in both sexes, depletion of skin Cyanobacteria decreased the protection from hypertension in the RNO5 female, but not male, congenic strain. In conclusion, to our knowledge this is the first study to identify specific microbiota in sites other than gut as contributors to BP regulation. Notably, both oral Actinobacteria and skin Cyanobacteria were beneficial for lowering BP.

Entities:  

Keywords:  blood pressure; cardiovascular; dermal; microbiome; salt-sensitive

Mesh:

Substances:

Year:  2022        PMID: 35503026      PMCID: PMC9208435          DOI: 10.1152/physiolgenomics.00169.2021

Source DB:  PubMed          Journal:  Physiol Genomics        ISSN: 1094-8341            Impact factor:   4.297


  39 in total

1.  (23)Na magnetic resonance imaging of tissue sodium.

Authors:  Christoph Kopp; Peter Linz; Lydia Wachsmuth; Anke Dahlmann; Thomas Horbach; Christof Schöfl; Wolfgang Renz; Davide Santoro; Thoralf Niendorf; Dominik N Müller; Myriam Neininger; Alexander Cavallaro; Kai-Uwe Eckardt; Roland E Schmieder; Friedrich C Luft; Michael Uder; Jens Titze
Journal:  Hypertension       Date:  2011-12-05       Impact factor: 10.190

2.  Two linked blood pressure quantitative trait loci on chromosome 10 defined by dahl rat congenic strains.

Authors:  M R Garrett; X Zhang; O I Dukhanina; A Y Deng; J P Rapp
Journal:  Hypertension       Date:  2001-10       Impact factor: 10.190

3.  Blood pressure and proteinuria effects of multiple quantitative trait loci on rat chromosome 9 that differentiate the spontaneously hypertensive rat from the Dahl salt-sensitive rat.

Authors:  Edward J Toland; Shane Yerga-Woolwine; Phyllis Farms; George T Cicila; Yasser Saad; Bina Joe
Journal:  J Hypertens       Date:  2008-11       Impact factor: 4.844

4.  23Na magnetic resonance imaging-determined tissue sodium in healthy subjects and hypertensive patients.

Authors:  Christoph Kopp; Peter Linz; Anke Dahlmann; Matthias Hammon; Jonathan Jantsch; Dominik N Müller; Roland E Schmieder; Alexander Cavallaro; Kai-Uwe Eckardt; Michael Uder; Friedrich C Luft; Jens Titze
Journal:  Hypertension       Date:  2013-01-21       Impact factor: 10.190

5.  Multiple blood pressure QTL on rat chromosome 1 defined by Dahl rat congenic strains.

Authors:  Y Saad; M R Garrett; J P Rapp
Journal:  Physiol Genomics       Date:  2001-01-19       Impact factor: 3.107

6.  Olfactory receptor responding to gut microbiota-derived signals plays a role in renin secretion and blood pressure regulation.

Authors:  Jennifer L Pluznick; Ryan J Protzko; Haykanush Gevorgyan; Zita Peterlin; Arnold Sipos; Jinah Han; Isabelle Brunet; La-Xiang Wan; Federico Rey; Tong Wang; Stuart J Firestein; Masashi Yanagisawa; Jeffrey I Gordon; Anne Eichmann; Janos Peti-Peterdi; Michael J Caplan
Journal:  Proc Natl Acad Sci U S A       Date:  2013-02-11       Impact factor: 11.205

7.  Characterization of the rat oral microbiome and the effects of dietary nitrate.

Authors:  Embriette R Hyde; Berkley Luk; Stanley Cron; Lenka Kusic; Tyler McCue; Tonya Bauch; Heidi Kaplan; Gena Tribble; Joseph F Petrosino; Nathan S Bryan
Journal:  Free Radic Biol Med       Date:  2014-10-12       Impact factor: 7.376

8.  Gut microbiota dysbiosis contributes to the development of hypertension.

Authors:  Jing Li; Fangqing Zhao; Yidan Wang; Junru Chen; Jie Tao; Gang Tian; Shouling Wu; Wenbin Liu; Qinghua Cui; Bin Geng; Weili Zhang; Ryan Weldon; Kelda Auguste; Lei Yang; Xiaoyan Liu; Li Chen; Xinchun Yang; Baoli Zhu; Jun Cai
Journal:  Microbiome       Date:  2017-02-01       Impact factor: 14.650

9.  Gut Microbiota-Related Evidence Provides New Insights Into the Association Between Activating Transcription Factor 4 and Development of Salt-Induced Hypertension in Mice.

Authors:  Tian-Hao Liu; Wen-Cong Tao; Qiu-Er Liang; Wan-Qing Tu; Ya Xiao; Li-Guo Chen
Journal:  Front Cell Dev Biol       Date:  2020-11-13

Review 10.  Targeting Gut Microbiota to Treat Hypertension: A Systematic Review.

Authors:  Joonatan Palmu; Leo Lahti; Teemu Niiranen
Journal:  Int J Environ Res Public Health       Date:  2021-01-30       Impact factor: 3.390

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