Myeloid sirtuinl deficiency aggravates hippocampal inflammation in mice fed high-fat diets
- Authors
- Kim, Kyung Eun; Jeong, Eun Ae; Lee, Jong Youl; Yi, Chin-ok; Park, Kyung-ah; Jin, Zhen; Lee, Jung Eun; Horvath, 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.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - College of Medicine > Department of Medicine > Journal Articles

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.