Molecular hydrogen supplementation in mice ameliorates lipopolysaccharide‐induced loss of interest

Author:

Koga Minori1ORCID,Sato Mayumi1,Nakagawa Ryuichi1,Tokuno Shinichi23,Asai Fumiho1,Maezawa Yuri1,Nagamine Masanori4ORCID,Yoshino Aihide1,Toda Hiroyuki1

Affiliation:

1. Department of Psychiatry, School of Medicine National Defense Medical College Saitama Japan

2. Graduate School of Health Innovation Kanagawa University of Human Services Kanagawa Japan

3. Department of Bioengineering Graduate School of Engineering Tokyo Japan

4. Division of Behavioral Sciences National Defense Medical College Research Institute Saitama Japan

Abstract

AbstractAimThe objective of this study was to evaluate the potential of hydrogen in preventing and treating psychiatric symptoms, particularly depressed mood and loss of interest, and to explore its underlying mechanisms. A mouse model exhibiting inflammation‐derived depressive symptoms was used for the investigation.MethodsInstitute of Cancer Research mice were subjected to a 7‐day intervention of either 30% hydrogen or 40 g per day of air via jelly intake. On the final day, lipopolysaccharide (LPS) was intraperitoneally administered at 5 mg/kg to induce inflammation‐related depressive symptoms. Behavioral and biochemical assessments were conducted 24 h post‐LPS administration.ResultsFollowing LPS administration, a decrease in spontaneous behavior was observed; however, this effect was mitigated in the group treated with hydrogen. The social interaction test revealed a significant reduction in interactions with unfamiliar mice in the LPS‐treated group, whereas the hydrogen‐treated group exhibited no such decrease. No significant changes were noted in the forced‐swim test for either group. Additionally, the administration of LPS in the hydrogen group did not result in a decrease in zonula occludens‐1, a biochemical marker associated with barrier function at the cerebrovascular barrier and expressed in tight junctions.ConclusionHydrogen administration demonstrated a preventive effect against the LPS‐induced loss of interest, suggesting a potential role in symptom prevention. However, it did not exhibit a suppressive effect on depressive symptoms in this particular model. These findings highlight the nuanced impact of hydrogen in the context of inflammation‐induced psychiatric symptoms, indicating potential avenues for further exploration and research.

Publisher

Wiley

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