Evaluation of Anti-Diabetic Potential of Corn Silk in High-Fat Diet/Streptozotocin-Induced Type 2 Diabetes Mice Model

被引:11
|
作者
Sheng, Li [1 ]
Chen, Qian [1 ]
Di, Lei [1 ]
Li, Ning [1 ]
机构
[1] Anhui Med Univ, Sch Pharm, Anhui Key Lab Bioact Nat Prod, 81 Meishan Rd, Hefei 230032, Peoples R China
基金
美国国家科学基金会;
关键词
Corn silk; diabetes; high blood glucose; hyperlipidemia; insulin resistance; oxidative stress; APOPTOTIC CELL-DEATH; DYSLIPIDEMIA; PATHOPHYSIOLOGY; MAYSIN;
D O I
10.2174/1871530320666200606224708
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Corn silk is the elongated stigma of the female flower of Zea mays and traditionally used to treat diabetes mellitus (DM). Objective: To investigate the beneficial effects of corn silk extract (CSE) on IEFD/STZ-induced diabetic C56BL/6J mice. Methods: Establishment of a T2DM model through feeding BED combined with STZ. T2DM was randomly divided into 5 groups: diabetic control mice treated with vehicle (model group, n=10), metformin-treated group (metformin: 150 mg/kg.d, n=10), three CS-treated groups (CS: 300, 600 and 1200 mg/kg.d, n=10). After four weeks of CS treatment, the body weight, FBG, IR, TC, TG, LDL-C, MDA and SOD levels of mice were measured. In addition, the liver tissue was histomorphologically analyzed by HE stain followed a light microscopy observation. Results: 4-week CSE treatment significantly reduced FBG and enhanced the glucose tolerance; improved IR indicated by decreased HOMA-IR and elevated ISI; alleviated hyperlipidemia indicated by decreased TC, TO, LDL-C, and increased HDL-C; reduced oxidative stress by decreased MDA and elevated SOD activity; decreased hepatic lipid accumulation and prevented liver tissue morphological change in T2DM. In addition, CSE treatments effectively prevent the weight gain loss of diabetic mice. Conclusion: These results confirmed the traditionally claimed benefits of corn silk on DM, which suggested that the corn silk possessed the anti-diabetic potential and could be further developed as a cheap and plant-derived agent for the treatment of type 2 diabetes mellitus.
引用
收藏
页码:131 / 138
页数:8
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