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Cited 17 time in webofscience Cited 17 time in scopus
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Myeloid sirtuinl deficiency aggravates hippocampal inflammation in mice fed high-fat diets

Authors
Kim, Kyung EunJeong, Eun AeLee, Jong YoulYi, Chin-okPark, Kyung-ahJin, ZhenLee, Jung EunHorvath, Tamas L.Roh, Gu Seob
Issue Date
May-2018
Publisher
Academic Press
Keywords
Obesity; SIRT1; Lipocalin-2; Insulin resistance; Inflammation; Hippocampus
Citation
Biochemical and Biophysical Research Communications, v.499, no.4, pp 1025 - 1031
Pages
7
Indexed
SCI
SCIE
SCOPUS
Journal Title
Biochemical and Biophysical Research Communications
Volume
499
Number
4
Start Page
1025
End Page
1031
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/11641
DOI
10.1016/j.bbrc.2018.04.044
ISSN
0006-291X
1090-2104
Abstract
Chronic low-grade inflammation-induced insulin resistance is associated with neuroinflammation. Myeloid sirtuinl (SIRTI) deficiency aggravates high-fat diet (HFD)-induced insulin resistance. However, the function of myeloid-specific SIRTI in the hippocampus of obese mice is largely unknown. To address this question, we fed myeloid SIRTI knockout (KO) mice a HFD for 40 weeks. We found that HFD-fed SIRTI KO mice had increased insulin resistance and macrophage infiltration in adipose tissue than wild type (WT) mice. Levels of HFD-induced lipocalin-2 (LCN2) were lower in SIRT1 KO mice than in WT. HFD-induced hippocampal LCN2 expression was lower in HFD-fed SIRTI KO mice than in WT. Hippocampal acetylation of nuclear factor-kappa B (NF-kappa B) and amyloid precursor protein levels were higher in HFD-fed SIRT1 KO mice than in HFD-fed WT mice. Taken together, our results suggest that targeted induction of the anti-inflammatory effects of SIRTI and LCN2 may help prevent obesity-associated insulin resistance and neuroinflammation. (C) 2018 Elsevier Inc. All rights reserved.
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