Quercitrin Ameliorates Hyperlipidemia and Hepatic Steatosis in Ovariectomized Mice

被引:27
|
作者
Hur, Haeng Jeon [1 ]
Jeong, Yeon-Hui [1 ]
Lee, Sang Hee [1 ]
Sung, Mi Jeong [1 ]
机构
[1] Korea Food Res Inst, Food Funct Res, Res Grp Nat Mat & Metab, Jeollabuk Do 55365, South Korea
来源
LIFE-BASEL | 2020年 / 10卷 / 10期
关键词
quercitrin; lipid metabolism; estrogen deficiency; hepatic steatosis; inflammation; nonalcoholic fatty liver disease; FATTY LIVER-DISEASE; INFLAMMATION; FLAVONOIDS; ESTROGENS; CYTOKINES; IMPACT; RATS;
D O I
10.3390/life10100243
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nonalcoholic fatty liver disease (NAFLD) is associated with progressive metabolic diseases. Estrogen deficiency increases the NAFLD risk among postmenopausal women. Thus, effective agents to prevent and treat NAFLD in postmenopausal women are required. Quercitrin (Quer) is a natural glycosylated flavonoid with antimicrobial, anti-inflammatory, and hypolipidemic effects. This study investigated whether Quer improves dysregulated lipid metabolism and suppresses hepatic steatosis in ovariectomized (OVX) mice as an experimental model mimicking postmenopausal women. Mice were assigned to the following four groups: SHAM, OVX, OVX + beta-estradiol (0.4 mg/kg diet), and OVX + Quer (500 mg/kg diet). Mice were administered a diet with or without Quer for three months. OVX mice displayed significantly higher body mass, epidermal fat, and liver weights than those of SHAM mice. However, these levels were reduced in Quer-treated mice. Quer treatment reduced the levels of serum lipid metabolites, including triglycerides, total cholesterol, and low-density lipoprotein cholesterol. Furthermore, Quer reduced liver lipid steatosis and inhibited the expression of proinflammatory cytokines, such as tumor necrosis factor-alpha, IL-6, and IL-1 beta. The results of the present study indicate that Quer improves dysregulated lipid metabolism and reduces hepatic steatosis and inflammation by compensating for estrogen deficiency, suggesting that Quer may potentially exert protective effects during hepatic steatosis in postmenopausal women.
引用
收藏
页码:1 / 9
页数:9
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