Protective effect of cinnamon polyphenols against STZ-diabetic mice fed high-sugar, high-fat diet and its underlying mechanism

被引:59
|
作者
Li, Rong [1 ]
Liang, Tao [2 ]
Xu, Lingyuan [3 ]
Li, Yongwen [4 ]
Zhang, Shijun [2 ]
Duan, Xiaoqun [4 ]
机构
[1] Guilin Med Univ, Dept Physiol, Guilin 541004, Guangxi, Peoples R China
[2] Guangxi Med Univ, Nanning 530021, Peoples R China
[3] YouJiang Med Univ Nationalities, Affiliated Hosp, Ctr Clin Lab, Baise 533000, Guangxi, Peoples R China
[4] Guilin Med Univ, Dept Pharmacol, Guilin 541004, Guangxi, Peoples R China
关键词
Cinnamon polyphenols; Pancreatic beta cell; Hypoglycemic effects; Hypolipidemic activity; iNOS; NF-kappa B; NF-KAPPA-B; INSULIN-RESISTANCE; TYPE-2; EXTRACT; GLUCOSE; OBESITY; ACTIVATION; MELLITUS; STRESS;
D O I
10.1016/j.fct.2012.10.024
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
This study was designed to investigate the potential effects of 14 days' intragastrically given of cinnamon polyphenols (CPS) in treating diabetic mice induced by intraperitoneal injection of streptozotocin (150 mg kg(-1)) and fed high-sugar, high-fat diet. The diabetic mice model was successfully established through determining on fasting blood-glucose (FBG) test. As revealed by glucose oxidase (GOD) and radioimmunoassay (RIA), both dimethyldiguanide (DC, 0.6 g kg(-1) d(-1)) and CPS (03, 0.6, 1.2 g k(-1) d(-1)) treatments significantly resulted in down-regulation of blood glucose and insulin levels in serum, while the levels of oxidative stress markers were markedly lowered through ELISA assay. Meanwhile, the pathological damage in islet with pancreatic beta cells was ameliorated by treatment of CPS at different doses, as shown in HE stain. At the same time, the treatments also caused notable reduction of iNOS, NF-kappa B expressions showing in Western blot analysis. These findings demonstrate that cinnamon polyphenols can exert the hypoglycemic and hypolipidemic effects through the mechanisms that may be associated with repairing pancreatic beta cells in diabetic mice and improving its anti-oxidative capacity, as well as attenuating cytotoxicity via inhibition of iNOS, NF-kappa B activation. Published by Elsevier Ltd.
引用
收藏
页码:419 / 425
页数:7
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