Abstract

A growing body of evidence suggests a relationship between olfactory dysfunction and the pathogenesis of mental disorders. Our previous studies indicated that chronic nasal inflammation caused loss of olfactory sensory neurons and gross atrophy of the olfactory bulb, which may lead to olfactory dysfunction. Simultaneously, increasing numbers of reports have elucidated the importance of gut microbiota to maintain brain function and that dysbiosis may be associated with neuropsychiatric disorders. Here we examined whether chronic nasal inflammation perturbed gut microbiota and whether there were sex differences in this pattern. Eight-week-old C57BL/6 mice repeatedly received bilateral nasal administration of lipopolysaccharide (LPS) 3 times/week to cause chronic nasal inflammation or saline as a control. At 9 weeks, cecal feces were used for 16S metagenomic analysis and whole blood and fresh tissue of spleen were used for ELISA analyses. Microbiome analysis demonstrated a remarkable change of the gut microbiota in male mice with chronic nasal inflammation which was different from that in female mice. In both mice, systemic inflammation did not occur. This has shown for the first time that chronic nasal inflammation correlates with sex-dependent changes in the gut microbiota. The detailed mechanism and potential alteration to brain functions await further studies.

Highlights

  • A growing body of evidence suggests a relationship between olfactory dysfunction and the pathogenesis of mental disorders

  • We demonstrated that chronic nasal inflammation causes loss of olfactory sensory neurons (OSNs) and gross atrophy of the olfactory bulb (OB), the first relay station of the olfactory neurocircuit in the central nervous system

  • After repeated administration of lipopolysaccharide (LPS) to bilateral nostrils, inflammatory cells such as macrophages (F4/80-positive), neutrophils (Ly-6G-positive), T cells (CD3e-positive) and B cells (CD45R-positive) locally infiltrated some regions of the olfactory mucosa (OM) in male and female mice, while these cells were not observed in the OM of saline-treated mice (Supplementary Figure S1)

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Summary

Introduction

A growing body of evidence suggests a relationship between olfactory dysfunction and the pathogenesis of mental disorders. Microbiome analysis demonstrated a remarkable change of the gut microbiota in male mice with chronic nasal inflammation which was different from that in female mice. In both mice, systemic inflammation did not occur. We demonstrated that chronic nasal inflammation causes loss of olfactory sensory neurons (OSNs) and gross atrophy of the olfactory bulb (OB), the first relay station of the olfactory neurocircuit in the central nervous system. In the OB, glial cells were activated, pro-inflammatory cytokines were elevated, and subsequently tufted cell-related neurocircuits underwent degeneration in a mouse model with chronic nasal i­nflammation[6,7,8] These results suggest that an olfactory neural pathway is a route through which nasal inflammation damages the brain. Other factors perturbing adult gut microbiota are not well documented

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