MyD88 determines the protective effects of fish oil and perilla oil against metabolic disorders and inflammation in adipose tissue from mice fed a high-fat diet

被引:17
|
作者
Wang, Feng [1 ,2 ,3 ]
Hu, Mingyuan [1 ,2 ,4 ]
Zhu, Hangju [1 ,2 ,5 ]
Yang, Chao [1 ,2 ]
Xia, Hui [1 ,2 ]
Yang, Xian [1 ,2 ]
Yang, Ligang [1 ,2 ]
Sun, Guiju [1 ,2 ]
机构
[1] Southeast Univ, Sch Publ Hlth, Minist Educ, Key Lab Environm Med & Engn, Nanjing, Peoples R China
[2] Southeast Univ, Sch Publ Hlth, Dept Nutr & Food Hyg, Nanjing, Peoples R China
[3] Tianjin Inst Environm & Operat Med, Tianjin, Peoples R China
[4] Wannan Med Coll, Wuhu, Peoples R China
[5] Jiangsu Canc Hosp, Nanjing, Peoples R China
基金
中国国家自然科学基金;
关键词
INSULIN-RESISTANCE; ACIDS; SUPPLEMENTATION; OBESITY; LIPIDS; TLR4;
D O I
10.1038/s41387-021-00159-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The beneficial effects of omega-3 polyunsaturated fatty acids (PUFA) vary between different sources. However, there is a paucity of comparative studies regarding the effects and mechanisms of marine and plant omega-3 PUFA on obesity. Objective The aim of this study was to evaluate the effects of fish oil (FO) and perilla oil (PO) on glucolipid metabolism, inflammation, and adipokine in mice fed a high-fat (HF) diet in association with the contribution of toll-like receptor 4 (TLR4)/myeloid differentiation primary response 88 (MyD88) pathway. Methods C57BL/6J mice and MyD88-/- mice were randomly divided into 4 groups: normal chow diet, HF diet, HF diet accompanied by daily gavage with either FO or PO. After 4 weeks, blood biochemistries, adipocyte histology, mRNA, and protein expression of MyD88-dependent and -independent pathways of TLR4 signaling in epididymal adipose tissue were measured. Results In C57BL/6J mice, there were no statistical differences between FO and PO in decreasing body weight, glucose, insulin, triglyceride, total cholesterol, interleukin-6, and increasing adipocyte counts. FO and PO decreased mRNA and protein expression of TLR4, MyD88, tumor necrosis factor receptor-associated factor 6, inhibitor of nuclear factor kappa B kinase beta and nuclear factor-kappa B p65. In MyD88-/- mice, the beneficial effects of FO and PO on HF diet-induced metabolism abnormalities and inflammation were abolished. FO and PO had no impacts on mRNA and protein expression of receptor-interacting protein-1, interferon regulate factor 3, and nuclear factor-kappa B p65. Conclusion FO and PO exhibit similar protective effects on metabolic disorders and inflammation through inhibiting TLR4 signaling in a manner dependent on MyD88. These findings highlight plant omega-3 PUFA as an attractive alternative source of marine omega-3 PUFA and reveal a mechanistic insight for preventive benefits of omega-3 PUFA in obesity and related metabolic diseases.
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页数:9
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