| Literature DB >> 33069781 |
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.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