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Título

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

AutorO'Connor, K.M.; Lucking, E.F.; Golubeva, Anna V.; Strain, C.R.; Fouhy, F.; Cénit, M. Carmen CSIC ORCID; Dhaliwal, P.; Bastiaanssen, T.F.S.; Burns, D.P.; Stanton, C.; Clarke, Gerard; Cryan, John F.; O'Halloran, K.D.
Palabras claveAntibiotics
Faecal microbiota transfer
Breathing
Hypercapnia
Cardiovascular
Vagus
Neurochemistry
Intestinal permeability
Microbiota
Fecha de publicación2019
EditorElsevier
CitaciónEBioMedicine (2019)
ResumenBackground: 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.
Versión del editorhttp://dx.doi.org/10.1016/j.ebiom.2019.03.029
URIhttp://hdl.handle.net/10261/201303
DOI10.1016/j.ebiom.2019.03.029
Identificadoresdoi: 10.1016/j.ebiom.2019.03.029
issn: 2352-3964
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