Quercetin reduces obesity-associated ATM infiltration and inflammation in mice: a mechanism including AMPKα1/SIRT1

被引:267
作者
Dong, Jing [1 ]
Zhang, Xian [1 ]
Zhang, Lei [1 ]
Bian, Hui-Xi [1 ]
Xu, Na [1 ]
Bao, Bin [1 ]
Liu, Jian [1 ]
机构
[1] Hefei Univ Technol, Sch Biotechnol & Food Engn, Hefei 230009, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金; 中国博士后科学基金;
关键词
obesity; insulin resistance; adipose tissue macrophage; macrophages; adenosine monophosphate-activated protein kinase alpha 1/silent information regulator 1; HIGH-FAT DIET; ACTIVATED PROTEIN-KINASE; ADIPOSE-TISSUE INFLAMMATION; NECROSIS-FACTOR-ALPHA; MACROPHAGE POLARIZATION; INSULIN-RESISTANCE; METABOLIC SYNDROME; NONALCOHOLIC STEATOHEPATITIS; ENERGY-EXPENDITURE; GLUCOSE-TOLERANCE;
D O I
10.1194/jlr.M038786
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Adipose tissue macrophage (ATM) plays a central role in obesity-associated inflammation and insulin resistance. Quercetin, a dietary flavonoid, possesses anti-inflammation and anti-insulin resistance properties. However, it is unclear whether quercetin can alleviate high-fat diet (HFD)-induced ATM infiltration and inflammation in mice. In this study, 5-week-old C57BL/6 mice were fed low-fat diet, HFD, or HFD with 0.l% quercetin for 12 weeks, respectively. Dietary quercetin reduced HFD-induced body weight gain and improved insulin sensitivity and glucose intolerance in mice. Meanwhile, dietary quercetin enhanced glucose transporter 4 translocation and protein kinase B signal in epididymis adipose tissues (EATs), suggesting that it heightened glucose uptake in adipose tissues. Histological and real-time PCR analysis revealed that quercetin attenuated mast cell and macrophage infiltration into EATs in HFD-fed mice. Dietary quercetin also modified the phenotype ratio of M1/M2 macrophages, lowered the levels of proinflammatory cytokines, and enhanced adenosine monophosphate-activated protein kinase (AMPK) alpha 1 phosphorylation and silent information regulator 1 (SIRT1) expression in EATs. Further, using AMPK activator 5-aminoimidazole-4-carboxamide-1-beta 4-ribofuranoside and inhibitor Compound C, we found that quercetin inhibited polarization and inflammation of mouse bone marrow-derived macrophages through an AMPK alpha 1/SIRT1-mediated mechanism.(jlr) In conclusion, dietary quercetin might suppress ATM infiltration and inflammation through the AMPK alpha 1/SIRT1 pathway in HFD-fed mice
引用
收藏
页码:363 / 374
页数:12
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