Chitooligosaccharide Biguanidine Alleviates Liver Injury and Insulin Resistance in Type 2 Diabetic Rats

被引:2
|
作者
Zhao, Liyan [1 ]
Zheng, Qifang [1 ]
Zou, Yalu [1 ]
Wang, Yuanyuan [1 ]
Wu, Yuntang [2 ]
Liu, Xiaofei [1 ]
机构
[1] Tianjin Univ, Sch Mat Sci & Engn, Tianjin Key Lab Composite & Funct Mat, Tianjin 300350, Peoples R China
[2] Tianjin Med Univ, Sch Publ Hlth, Dept Nutr & Food Sci, Tianjin 300070, Peoples R China
来源
STARCH-STARKE | 2020年 / 72卷 / 1-2期
基金
中国国家自然科学基金;
关键词
chitooligosaccharide biguanidine; glucose transporter 2; insulin resistance; liver injury; type 2 diabetes mellitus; GLUCOSE-HOMEOSTASIS; OXIDATIVE STRESS; HIGH-FAT; EXPRESSION; HYPERGLYCEMIA; GLUT2; MECHANISMS; PATHWAY; ACID; METABOLISM;
D O I
10.1002/star.201900203
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Chitooligosaccharide biguanidine (COSG) is a derivative of chitooligosaccharide that has been proven to have antidiabetic activity. In this study, the therapeutic effects of COSG on liver injury and insulin resistance are evaluated, and the possible mechanism is explored. Streptozotocin-induced diabetic rats are treated with COSG for 8 weeks. COSG treatment significantly increases the activity of catalase, superoxide dismutase, and glutathione peroxidase and inhibits the activity of malonic dialdehyde. Histological observation reveals that COSG treatment also alleviates the probability of hepatocyte degeneration or necrosis. Furthermore, COSG treatment significantly activates the insulin receptor substrate-2/phosphatidylinositol 3 kinase/protein kinase B signaling pathway and increases the glucose transporter 2/glucokinase expressions, which regulates liver glucose conversion and insulin secretion, COSG treatment also inhibits the glucose-6-phosphatase/phosphoenolpyruvate carboxykinase activations, resulting in a reduced level of blood glucose. Accordingly, COSG can protect against liver dysfunction caused by type 2 diabetes.
引用
收藏
页数:8
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