Abstract

Psychiatric disorders including depression and anxiety comprise a broad range of conditions with different symptoms. We have developed a mouse model of depression/anxiety in mice deficient in the St3gal4 gene. In this study, we performed a comparative analysis of urinary volatile organic compounds (VOCs) in St3gal4-deficient (St3gal4-KO) and wild-type mice using gas chromatography-mass spectrometry, and we screened 18 putative VOCs. Principal component analysis (PCA) based on these VOCs identified a major group of 11 VOCs, from which two groups were clarified by hierarchical clustering analysis. One group including six VOCs (pentanoic acid, 4-methyl-, ethyl ester; 3-heptanone, 6-methyl; benzaldehyde; 5,9-undecadien-2-ol, 6,10-dimethyl; and unknown compounds RI1291 and RI1237) was correlated with the startle response (r = 0.620), which is related to an unconscious defensive response. The other group including two VOCs (beta-farnesene and alpha-farnesene) comprised pheromones which increased in KO mice. Next, male mice underwent a social behavior test with female mice in the estrus stage, showing reduced access of KO male mice to female mice. Comparative analysis of urinary VOCs before and after encounters revealed that the six VOCs were not changed by these encounters. However, in WT mice, the two farnesenes increased after the encounters, reaching the level observed in KO mice, which was not altered following the encounter. Taken together, these results indicated that St3gal4 was involved in modulating urinary VOCs. Moreover, VOC clusters discovered by comparison of St3gal4-KO mice with WT mice were correlated with differential emotional behaviors.

Highlights

  • Depression and anxiety are common mental disorders that co-occur frequently [1], and they have been identified as a leading cause of burden globally [2]

  • We aimed to investigate metabolic changes related to metabolism in St3gal4-KO mice by directly evaluating volatile organic compounds (VOCs) as end-metabolites using solid-phase micro-extraction (SPME) to extract urinary VOCs [33] followed by gas chromatography-mass spectrometry (GC-MS) to screen for differential

  • The representative total ion current (TIC) peaks and list of VOCs estimated by a similarity index above 85% from experiment 1 and experiment 2 are shown in Figs 1 and S1

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Summary

Introduction

Depression and anxiety are common mental disorders that co-occur frequently [1], and they have been identified as a leading cause of burden globally [2]. Depression is a psychiatric disorder that is characterized by a depressed mood and/or loss of interest or pleasure and causes severe symptoms that affect daily activities, such as sleeping, eating, or working. In order to help patients who suffer from mental illness, it is important to deepen our understanding of the molecular mechanisms underlying psychiatric disorders and to investigate the potential mechanisms of action of drugs in patients with these disorders. We previously reported that ST3 beta-galactoside alpha-2,3-sialyltransferase IV (St3gal4)deficient mice showed symptoms of anxiety and depression [5].

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