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Chia oil supplementation changes body composition and activates insulin signaling cascade in skeletal muscle tissue of obese animals

Authors :
Simone Vargas da Silva
Christina Barja-Fidalgo
Thamiris de Souza
Thaís Fonte-Faria
Helena Fonseca Raposo
Lilia Zago
Georgia C. Atella
Marta Citelli
Source :
Nutrition. 58:167-174
Publication Year :
2019
Publisher :
Elsevier BV, 2019.

Abstract

Objective Chia seed oil is the richest source of plant-based ω-3 fatty acid, α-linolenic acid, but its potential and mechanisms of action to treat obesity are unclear. The aim of the study was to evaluate the effects of chia oil (ChOi) supplementation on body composition and insulin signaling in skeletal muscles of obese mice. Methods Male C57 BL/6 mice (n = 8/group) were fed regular control chow or a high-fat diet (HFD) for 135 d. Another HFD group additionally received ChOi from 90 to 135 d. Results Consumption of ChOi reduced fat mass accumulation and increased lean mass as evidenced by nuclear magnetic resonance. Moreover, obese mice treated with ChOi showed higher tyrosine phosphorylation of insulin receptor substrate 1, greater activation of protein kinase B, and increased translocation of glucose transporter type 4 in skeletal muscle tissue in response to insulin. ChOi supplementation improved glucose levels and insulin tolerance; decreased serum insulin, leptin, and triacylglycerols; and increased blood high-density lipoprotein cholesterol levels. All these effects caused by the use of ChOi seemed to be independent of the resolution of inflammation because the markers of inflammation were not altered in animals fed the HFD. Conclusion The molecular effects observed in muscle tissue together with changes in body composition may have contributed to the increased glucose tolerance and to the healthy phenotype presented by obese animals treated with ChOi.

Details

ISSN :
08999007
Volume :
58
Database :
OpenAIRE
Journal :
Nutrition
Accession number :
edsair.doi.dedup.....c861d07c2708032e540bdbd3ef8eab78
Full Text :
https://doi.org/10.1016/j.nut.2018.08.011