Manipulation of gut microbiota blunts the ventilatory response to hypercapnia in adult rats

Background: It is increasingly evident that perturbations to the diversity and composition of the gut microbiota have significant consequences for the regulation of integrative physiological systems. There is growing interest in the potential contribution of microbiota-gut-brain signalling to cardiorespiratory control in health and disease. Methods: In adult male rats, we sought to determine the cardiorespiratory effects of manipulation of the gut microbiota following a 4-week administration of a cocktail of antibiotics. We subsequently explored the effects of administration of faecal microbiota from pooled control (vehicle) rat faeces, given by gavage to vehicle- and antibiotic-treated rats. Findings: Antibiotic intervention depressed the ventilatory response to hypercapnic stress in conscious animals, owing to a reduction in the respiratory frequency response to carbon dioxide. Baseline frequency, respiratory timing variability, and the expression of apnoeas and sighs were normal. Microbiota-depleted rats had decreased systolic blood pressure. Faecal microbial transfer to vehicle- and antibiotic-treated animals also disrupted the gut microbiota composition, associated with depressed ventilatory responsiveness to hypercapnia. Chronic antibiotic intervention or faecal microbial transfer both caused significant disruptions to brainstem monoamine neurochemistry, with increased homovanillic acid:dopamine ratio indicative of increased dopamine turnover, which correlated with the abundance of several bacteria of six different phyla. Interpretation: Chronic antibiotic administration and faecal microbial transfer disrupt gut microbiota, brainstem monoamine concentrations and the ventilatory response to hypercapnia. We suggest that aberrant microbiota-gut-brain axis signalling has a modulatory influence on respiratory behaviour during hypercapnic stress. Fund: Department of Physiology and APC Microbiome Ireland, University College Cork, Ireland.

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Main Authors: O'Connor, K.M., Lucking, E.F., Golubeva, Anna V., Strain, C.R., Fouhy, F., Cénit, M. Carmen, Dhaliwal, P., Bastiaanssen, T.F.S., Burns, D.P., Stanton, C., Clarke, Gerard, Cryan, John F., O'Halloran, K.D.
Other Authors: Science Foundation Ireland
Format: artículo biblioteca
Published: Elsevier 2019
Subjects:Antibiotics, Faecal microbiota transfer, Breathing, Hypercapnia, Cardiovascular, Vagus, Neurochemistry, Intestinal permeability, Microbiota,
Online Access:http://hdl.handle.net/10261/201303
http://dx.doi.org/10.13039/501100001602
http://dx.doi.org/10.13039/501100001636
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spelling dig-iata-es-10261-2013032022-08-19T08:34:43Z Manipulation of gut microbiota blunts the ventilatory response to hypercapnia in adult rats O'Connor, K.M. Lucking, E.F. Golubeva, Anna V. Strain, C.R. Fouhy, F. Cénit, M. Carmen Dhaliwal, P. Bastiaanssen, T.F.S. Burns, D.P. Stanton, C. Clarke, Gerard Cryan, John F. O'Halloran, K.D. Science Foundation Ireland University College Cork Antibiotics Faecal microbiota transfer Breathing Hypercapnia Cardiovascular Vagus Neurochemistry Intestinal permeability Microbiota Background: It is increasingly evident that perturbations to the diversity and composition of the gut microbiota have significant consequences for the regulation of integrative physiological systems. There is growing interest in the potential contribution of microbiota-gut-brain signalling to cardiorespiratory control in health and disease. Methods: In adult male rats, we sought to determine the cardiorespiratory effects of manipulation of the gut microbiota following a 4-week administration of a cocktail of antibiotics. We subsequently explored the effects of administration of faecal microbiota from pooled control (vehicle) rat faeces, given by gavage to vehicle- and antibiotic-treated rats. Findings: Antibiotic intervention depressed the ventilatory response to hypercapnic stress in conscious animals, owing to a reduction in the respiratory frequency response to carbon dioxide. Baseline frequency, respiratory timing variability, and the expression of apnoeas and sighs were normal. Microbiota-depleted rats had decreased systolic blood pressure. Faecal microbial transfer to vehicle- and antibiotic-treated animals also disrupted the gut microbiota composition, associated with depressed ventilatory responsiveness to hypercapnia. Chronic antibiotic intervention or faecal microbial transfer both caused significant disruptions to brainstem monoamine neurochemistry, with increased homovanillic acid:dopamine ratio indicative of increased dopamine turnover, which correlated with the abundance of several bacteria of six different phyla. Interpretation: Chronic antibiotic administration and faecal microbial transfer disrupt gut microbiota, brainstem monoamine concentrations and the ventilatory response to hypercapnia. We suggest that aberrant microbiota-gut-brain axis signalling has a modulatory influence on respiratory behaviour during hypercapnic stress. Fund: Department of Physiology and APC Microbiome Ireland, University College Cork, Ireland. This project was funded by the Department of Physiology, and the APC Microbiome Ireland (funded by Science Foundation Ireland (SFI/12/RC/2273)), University College Cork, Ireland. 2020-02-20T08:29:22Z 2020-02-20T08:29:22Z 2019 2020-02-20T08:29:22Z artículo http://purl.org/coar/resource_type/c_6501 doi: 10.1016/j.ebiom.2019.03.029 issn: 2352-3964 EBioMedicine (2019) http://hdl.handle.net/10261/201303 10.1016/j.ebiom.2019.03.029 http://dx.doi.org/10.13039/501100001602 http://dx.doi.org/10.13039/501100001636 30898652 Publisher's version http://dx.doi.org/10.1016/j.ebiom.2019.03.029 Sí open Elsevier
institution IATA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-iata-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del IATA España
topic Antibiotics
Faecal microbiota transfer
Breathing
Hypercapnia
Cardiovascular
Vagus
Neurochemistry
Intestinal permeability
Microbiota
Antibiotics
Faecal microbiota transfer
Breathing
Hypercapnia
Cardiovascular
Vagus
Neurochemistry
Intestinal permeability
Microbiota
spellingShingle Antibiotics
Faecal microbiota transfer
Breathing
Hypercapnia
Cardiovascular
Vagus
Neurochemistry
Intestinal permeability
Microbiota
Antibiotics
Faecal microbiota transfer
Breathing
Hypercapnia
Cardiovascular
Vagus
Neurochemistry
Intestinal permeability
Microbiota
O'Connor, K.M.
Lucking, E.F.
Golubeva, Anna V.
Strain, C.R.
Fouhy, F.
Cénit, M. Carmen
Dhaliwal, P.
Bastiaanssen, T.F.S.
Burns, D.P.
Stanton, C.
Clarke, Gerard
Cryan, John F.
O'Halloran, K.D.
Manipulation of gut microbiota blunts the ventilatory response to hypercapnia in adult rats
description Background: It is increasingly evident that perturbations to the diversity and composition of the gut microbiota have significant consequences for the regulation of integrative physiological systems. There is growing interest in the potential contribution of microbiota-gut-brain signalling to cardiorespiratory control in health and disease. Methods: In adult male rats, we sought to determine the cardiorespiratory effects of manipulation of the gut microbiota following a 4-week administration of a cocktail of antibiotics. We subsequently explored the effects of administration of faecal microbiota from pooled control (vehicle) rat faeces, given by gavage to vehicle- and antibiotic-treated rats. Findings: Antibiotic intervention depressed the ventilatory response to hypercapnic stress in conscious animals, owing to a reduction in the respiratory frequency response to carbon dioxide. Baseline frequency, respiratory timing variability, and the expression of apnoeas and sighs were normal. Microbiota-depleted rats had decreased systolic blood pressure. Faecal microbial transfer to vehicle- and antibiotic-treated animals also disrupted the gut microbiota composition, associated with depressed ventilatory responsiveness to hypercapnia. Chronic antibiotic intervention or faecal microbial transfer both caused significant disruptions to brainstem monoamine neurochemistry, with increased homovanillic acid:dopamine ratio indicative of increased dopamine turnover, which correlated with the abundance of several bacteria of six different phyla. Interpretation: Chronic antibiotic administration and faecal microbial transfer disrupt gut microbiota, brainstem monoamine concentrations and the ventilatory response to hypercapnia. We suggest that aberrant microbiota-gut-brain axis signalling has a modulatory influence on respiratory behaviour during hypercapnic stress. Fund: Department of Physiology and APC Microbiome Ireland, University College Cork, Ireland.
author2 Science Foundation Ireland
author_facet Science Foundation Ireland
O'Connor, K.M.
Lucking, E.F.
Golubeva, Anna V.
Strain, C.R.
Fouhy, F.
Cénit, M. Carmen
Dhaliwal, P.
Bastiaanssen, T.F.S.
Burns, D.P.
Stanton, C.
Clarke, Gerard
Cryan, John F.
O'Halloran, K.D.
format artículo
topic_facet Antibiotics
Faecal microbiota transfer
Breathing
Hypercapnia
Cardiovascular
Vagus
Neurochemistry
Intestinal permeability
Microbiota
author O'Connor, K.M.
Lucking, E.F.
Golubeva, Anna V.
Strain, C.R.
Fouhy, F.
Cénit, M. Carmen
Dhaliwal, P.
Bastiaanssen, T.F.S.
Burns, D.P.
Stanton, C.
Clarke, Gerard
Cryan, John F.
O'Halloran, K.D.
author_sort O'Connor, K.M.
title Manipulation of gut microbiota blunts the ventilatory response to hypercapnia in adult rats
title_short Manipulation of gut microbiota blunts the ventilatory response to hypercapnia in adult rats
title_full Manipulation of gut microbiota blunts the ventilatory response to hypercapnia in adult rats
title_fullStr Manipulation of gut microbiota blunts the ventilatory response to hypercapnia in adult rats
title_full_unstemmed Manipulation of gut microbiota blunts the ventilatory response to hypercapnia in adult rats
title_sort manipulation of gut microbiota blunts the ventilatory response to hypercapnia in adult rats
publisher Elsevier
publishDate 2019
url http://hdl.handle.net/10261/201303
http://dx.doi.org/10.13039/501100001602
http://dx.doi.org/10.13039/501100001636
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