FAHFA footprint in the visceral fat of mice across their lifespan.


Journal

Biochimica et biophysica acta. Molecular and cell biology of lipids
ISSN: 1879-2618
Titre abrégé: Biochim Biophys Acta Mol Cell Biol Lipids
Pays: Netherlands
ID NLM: 101731727

Informations de publication

Date de publication:
05 2020
Historique:
received: 12 07 2019
revised: 20 01 2020
accepted: 23 01 2020
pubmed: 29 1 2020
medline: 28 10 2020
entrez: 29 1 2020
Statut: ppublish

Résumé

Fatty acid esters of hydroxy fatty acids (FAHFAs) are a new class of endogenous lipids with anti-inflammatory and anti-diabetic effects, having the potential to treat type 2 diabetes (T2D). In view of the important regulatory and therapeutic actions of FAHFAs on age-related diseases such as T2D, we hypothesized that they may also play crucial roles in the growth, development, and aging process. Here, we investigated the FAHFA footprint in the visceral adipose tissue (VAT) of mice across lifespan to attain potential clues for understanding the roles of FAHFAs in growth, development, and aging using chemical isotope labeling assisted liquid chromatography-mass spectrometry. VAT samples were harvested from 80 C57BL/6J male mice of nine different ages (1, 2, 3, 6, 9, 12, 15, 18, and 24 months). The results showed that a total of 51 FAHFA families, including 301 regioisomers, were detected in the VAT of mice of all ages, and the number of FAHFAs (both family and regioisomer) in VAT increased with age, from 35 families (186 ± 0 regioisomers) at 1-month-old mice to 46 families (278 ± 6 regioisomers) in 18-month-old mice. Furthermore, the content of 12 FAHFA families per 100 mg of VAT of mice was highly correlated with age, and was usually low in the middle-age (3-15 months). However, because the VAT mass was 4-5 fold higher in middle-aged mice compared to younger or older mice, the total amount of most of the FAHFA regioisomers in VAT was increased in middle-aged mice. To the best of our knowledge, this is the first study to show that the number of regioisomers from 51 FAHFA families and abundance of 15 FAHFA families are strongly dependent on age, which would be helpful for understanding the mechanisms underlying the effects of FAHFAs on growth, development, and aging.

Identifiants

pubmed: 31988049
pii: S1388-1981(20)30031-7
doi: 10.1016/j.bbalip.2020.158639
pii:
doi:

Substances chimiques

Esters 0
Fatty Acids 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

158639

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare no conflict of interest.

Auteurs

Quan-Fei Zhu (QF)

Department of Chemistry, Wuhan University, Wuhan 430072, PR China.

Jing-Wen Yan (JW)

Department of Chemistry, Wuhan University, Wuhan 430072, PR China.

Jian Ni (J)

Department of Chemistry, Wuhan University, Wuhan 430072, PR China.

Yu-Qi Feng (YQ)

Department of Chemistry, Wuhan University, Wuhan 430072, PR China; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan 430072, PR China. Electronic address: yqfeng@whu.edu.cn.

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