Literature DB >> 33069781

Neuroinflammaging underlies emotional disturbances and circadian rhythm disruption in young male senescence-accelerated mouse prone 8 mice.

Naoki Ito1, Hiroaki Takemoto2, Ayana Hasegawa3, Chika Sugiyama4, Kengo Honma4, Takayuki Nagai5, Yoshinori Kobayashi6, Hiroshi Odaguchi7.   

Abstract

Aging causes psychological dysfunction and neurodegeneration, and can lead to cognitive impairments. Although numerous studies have reported that neurodegeneration and subsequent cognitive impairments are involved in neuroinflammation, relationship between psychological disturbance and neuroinflammation with aging (neuroinflammaging) remains unclear. Here, to clarify the relationship, we examined whether neuroinflammaging affects emotional behaviors in senescence-accelerated mouse prone 8 (SAMP8) mice. Microglial inflammatory responses to a subsequent lipopolysaccharide (LPS) challenge were significantly enhanced in male SAMP8 mice relative to normal aging senescence-accelerated mouse resistant 1 (SAMR1) mice at 17 weeks, but not 8 weeks of age. LPS injection also significantly increased brain and systemic inflammation in SAMP8 mice at 17 weeks. In a battery of behavioral tests, SAMP8 mice at 17 weeks, but not 8 weeks, exhibited anxiety- and depression-like behaviors and circadian rhythm disruption. Taken together, SAMP8 mice at 17 weeks possess a brain microenvironment in which it is easier to trigger neuroinflammatory priming; this may lead to an emergence of anxiety- and depression-like behaviors and circadian rhythm disruption. These findings provide new insights into the temporal relationship between neuroinflammaging and emotion.
Copyright © 2020. Published by Elsevier Inc.

Entities:  

Keywords:  Aging; Circadian rhythm; Depression; Microglia; Neuroinflammation; Senescence-accelerated mouse

Mesh:

Year:  2020        PMID: 33069781     DOI: 10.1016/j.exger.2020.111109

Source DB:  PubMed          Journal:  Exp Gerontol        ISSN: 0531-5565            Impact factor:   4.032


  3 in total

1.  Interleukin-1β Modulates Synaptic Transmission and Synaptic Plasticity During the Acute Phase of Sepsis in the Senescence-Accelerated Mouse Hippocampus.

Authors:  Koji Hoshino; Yuka Uchinami; Yosuke Uchida; Hitoshi Saito; Yuji Morimoto
Journal:  Front Aging Neurosci       Date:  2021-02-10       Impact factor: 5.750

2.  Microglial Hyperreactivity Evolved to Immunosuppression in the Hippocampus of a Mouse Model of Accelerated Aging and Alzheimer's Disease Traits.

Authors:  Patricia Molina-Martínez; Rubén Corpas; Elisa García-Lara; Marta Cosín-Tomás; Rosa Cristòfol; Perla Kaliman; Carme Solà; José Luis Molinuevo; Raquel Sánchez-Valle; Anna Antonell; Albert Lladó; Coral Sanfeliu
Journal:  Front Aging Neurosci       Date:  2021-01-28       Impact factor: 5.750

3.  Kampo formulas alleviate aging-related emotional disturbances and neuroinflammation in male senescence-accelerated mouse prone 8 mice.

Authors:  Naoki Ito; Akiko Maruko; Kenshiro Oshima; Masaaki Yoshida; Kengo Honma; Chika Sugiyama; Takayuki Nagai; Yoshinori Kobayashi; Hiroshi Odaguchi; Norihiro Okada
Journal:  Aging (Albany NY)       Date:  2022-01-03       Impact factor: 5.682

  3 in total

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