Allomyrina dichotoma Larva Extract Ameliorates the Hepatic Insulin Resistance of High-Fat Diet-Induced Diabetic Mice

被引:22
作者
Kim, Kyong [1 ]
Bae, Gong Deuk [2 ]
Lee, Minho [3 ]
Park, Eun-Young [4 ,5 ]
Baek, Dong Jae [4 ,5 ]
Kim, Chul Young [6 ]
Jun, Hee-Sook [2 ,7 ,8 ]
Oh, Yoon Sin [1 ]
机构
[1] Eulji Univ, Dept Food & Nutr, Seongnam 13135, South Korea
[2] Gachon Univ, Lee Gil Ya Canc & Diabet Inst, Dept Mol Med, Incheon 21999, South Korea
[3] Eulji Univ, Dept Food Technol & Serv, Seongnam 13135, South Korea
[4] Mokpo Natl Univ, Coll Pharm, Jeonnam 58554, South Korea
[5] Mokpo Natl Univ, Nat Med Res Inst, Jeonnam 58554, South Korea
[6] Hanyang Univ, Coll Pharm, Ansan 15888, South Korea
[7] Gachon Univ, Coll Pharm, Incheon 21936, South Korea
[8] Gachon Univ, Gachon Inst Pharmaceut Sci, Incheon 21936, South Korea
基金
新加坡国家研究基金会;
关键词
Allomyrina dichotoma larva; hepatic insulin resistance; lipogenesis; LIVER-DISEASE; PROTEIN-KINASE; IN-VITRO; CHOLESTEROL; BEETLE; PURIFICATION; HOMEOSTASIS; OBESITY; FAMILY; MODEL;
D O I
10.3390/nu11071522
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Allomyrina dichotoma larva is a nutritional-worthy future food resource and it contributes to multiple pharmacological functions. However, its antidiabetic effect and molecular mechanisms are not yet fully understood. Therefore, we investigated the hypolipidemic effect of A. dichotoma larva extract (ADLE) in a high-fat diet (HFD)-induced C57BL/6J mice model. Glucose tolerance and insulin sensitivity in HFD-induced diabetic mice significantly improved after ADLE administration for six weeks. The levels of serum triglyceride (TG), aspartate aminotransferase (AST), alanine transferase (ALT) activity, and lipid accumulation were increased in the liver of HFD-fed mice, but the levels were significantly reduced by the ADLE treatment. Moreover, hepatic fibrosis and inflammatory gene expression in the liver from HFD-treated mice were ameliorated by the ADLE treatment. Dephosphorylation of AMP-activated protein kinase (AMPK) by palmitate was inhibited in the ADLE treated HepG2 cells, and subsequently reduced expression of lipogenic genes, such as SREPBP-1c, ACC, and FAS were observed. The reduced expression of lipogenic genes and an increased phosphorylation of AMPK was also observed in the liver from diabetic mice treated with ADLE. In conclusion, ADLE ameliorates hyperlipidemia through inhibition of hepatic lipogenesis via activating the AMPK signaling pathway. These findings suggest that ADLE and its constituent bioactive compounds are valuable to prevent or treat hepatic insulin resistance in type 2 diabetes.
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页数:14
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