Fecal microbiota transplantation from mice exposed to chronic intermittent hypoxia elicits sleep disturbances in naïve mice.


Journal

Experimental neurology
ISSN: 1090-2430
Titre abrégé: Exp Neurol
Pays: United States
ID NLM: 0370712

Informations de publication

Date de publication:
12 2020
Historique:
received: 15 05 2020
revised: 21 07 2020
accepted: 18 08 2020
pubmed: 25 8 2020
medline: 11 3 2021
entrez: 25 8 2020
Statut: ppublish

Résumé

Obstructive sleep apnea (OSA) is a chronic prevalent condition characterized by intermittent hypoxia (IH) and sleep fragmentation (SF). Evidence suggests that OSA can alter the gut microbiome (GM) diversity and composition that may then promote the occurrence of some of the OSA-associated morbidities. However, it is unclear whether perturbations in the GM caused by IH can elicit sleep disturbances that underlie the increased sleep propensity that occurs in IH-exposed mice. To evaluate this issue, we exposed C57Bl/6 J mice to IH or room air (RA) for 6 weeks, and fecal matter was collected and frozen. C57Bl/6 J naïve mice were then randomly assigned to a fecal microbiota transfer (FMT) protocol for 3 weeks with either IH or RA fecal slur, and their GM was then analyzed using 16 s rRNA sequencing. In addition, FMT recipients underwent sleep recordings using piezoelectric approaches for 3 consecutive days. As anticipated, FMT-IH and FMT-RA mice showed different taxonomic profiles that corresponded to previous effects of IH on GM. Furthermore, FMT-IH mice exhibited increased sleep duration and the frequency of longer sleep bouts during the dark cycle, suggesting increased sleepiness (p < 0.0001 vs. FMT-RA mice). Thus, alterations of GM diversity induced by IH exposures can elicit sleep disturbances in the absence of concurrent IH, suggesting that sleep disturbances can be mediated, at least in part, by IH-induced alterations in GM.

Identifiants

pubmed: 32835671
pii: S0014-4886(20)30270-3
doi: 10.1016/j.expneurol.2020.113439
pmc: PMC7642108
mid: NIHMS1623175
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

113439

Subventions

Organisme : NHLBI NIH HHS
ID : R56 HL140548
Pays : United States
Organisme : NIA NIH HHS
ID : RF1 AG061824
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL130984
Pays : United States
Organisme : NIH HHS
ID : K01 OD019924
Pays : United States
Organisme : NIH HHS
ID : U42 OD010918
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Mohammad Badran (M)

Department of Child Health and Child Health Research Institute, Faculty of Medicine, University of Missouri, Columbia, MO 65201, United States.

Abdelnaby Khalyfa (A)

Department of Child Health and Child Health Research Institute, Faculty of Medicine, University of Missouri, Columbia, MO 65201, United States.

Aaron Ericsson (A)

Department of Veterinary Pathobiology, University of Missouri, Columbia, MO, United States; University of Missouri, Metagenomics Center, Columbia, MO, United States.

David Gozal (D)

Department of Child Health and Child Health Research Institute, Faculty of Medicine, University of Missouri, Columbia, MO 65201, United States. Electronic address: gozald@health.missouri.edu.

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