Journal
BRAIN BEHAVIOR AND IMMUNITY
Volume 98, Issue -, Pages 317-329Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbi.2021.08.228
Keywords
beta-naphthoflavone; Depression; Despair; Microbiota; Microbiota-gut-brain axis
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Funding
- Canadian Institutes of Health Research
- Canadian Institutes of Health Research Team Grant: Health Challenges in Chronic Inflammation
- National Council for Scientific and Technological Development (CNPq), Brazil
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The intestinal microbiota influences brain functions and behavior, with the aryl hydrocarbon receptor (Ahr) playing a crucial role in modulating microbiota-related alterations in behavior in male and female mice. Ahr activation can normalize despair behavior induced by antibiotic treatment, suggesting Ahr as a potential modulator of behavioral conditions influenced by the intestinal microbiota.
The intestinal microbiota plays an important role in regulating brain functions and behaviour. Microbiota-dependent changes in host physiology have been suggested to be key contributors to psychiatric conditions. However, specific host pathways modulated by the microbiota involved in behavioural control are lacking. Here, we assessed the role of the aryl hydrocarbon receptor (Ahr) in modulating microbiota-related alterations in behaviour in male and female mice after antibiotic (Abx) treatment. Mice of both sexes were treated with Abx to induce bacterial depletion. Mice were then tested in a battery of behavioural tests, including the elevated plus maze and open field tests (anxiety-like behaviour), 3 chamber test (social preference), and the tail suspension and forced swim tests (despair behaviour). Behavioural measurements in the tail suspension test were also performed after microbiota reconstitution and after administration of an Ahr agonist, beta-naphthoflavone. Gene expression analyses were performed in the brain, liver, and colon by qPCR. Abx-induced bacterial depletion did not alter anxiety-like behaviour, locomotion, or social preference in either sex. A sex-dependent effect was observed in despair behaviour. Male mice had a reduction in despair behaviour after Abx treatment in both the tail suspension and forced swim tests. A similar alteration in despair behaviour was observed in Ahr knockout mice. Despair behaviour was normalized by either microbiota recolonization or Ahr activation in Abx-treated mice. Ahr activation by beta-naphthoflavone was confirmed by increased expression of the Ahr-target genes Cyp1a1, Cyp1b1, and Ahrr. Our results demonstrate a role for Ahr in mediating the behaviours that are regulated by the crosstalk between the intestinal microbiota and the host. Ahr represents a novel potential modulator of behavioural conditions influenced by the intestinal microbiota.
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