Hypoglycemic activity and mechanism of the sulfated rhamnose polysaccharides chromium(III) complex in type 2 diabetic mice

被引:28
|
作者
Ye, Han [1 ]
Shen, Zhaopeng [2 ]
Cui, Jiefen [1 ]
Zhu, Yujie [1 ]
Li, Yuanyuan [1 ]
Chi, Yongzhou [1 ]
Wang, Jingfeng [1 ]
Wang, Peng [1 ]
机构
[1] Ocean Univ China, Coll Food Sci & Engn, 5 Yushan Rd, Qingdao 266003, Shandong, Peoples R China
[2] Ocean Univ China, Coll Med & Pharm, Qingdao 266003, Shandong, Peoples R China
关键词
Chromium; Glucose metabolism; Hypoglycemic; Mice; Sulfated rhamnose polysaccharides; FUCOSYLATED CHONDROITIN SULFATE; ENTEROMORPHA-PROLIFERA; INSULIN-RESISTANCE; III COMPLEX; METABOLISM; PICOLINATE;
D O I
10.1016/j.bioorg.2019.102942
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The sulfated rhamnose polysaccharides found in Enteromorpha prolifera belong to a class of unique polyanionic polysaccharides with high chelation capacity. In this study, a complex of sulfated rhamnose polysaccharides with chromium(III) (SRPC) was synthesized, and its effect on type 2 diabetes mellitus (T2DM) in mice fed a high-fat, high-sucrose diet was investigated. The molecular weight of SRPC is 4.57 kDa, and its chromium content is 28 mu g/mg. Results indicated that mice treated by oral administration of SRPC (10 mg/kg and 30 mg/kg body mass per day) for 11 weeks showed significantly improved oral glucose tolerance, decreased body mass gain, reduced serum insulin levels, and increased tissue glycogen content relative to T2DM mice (p < 0.01). SRPC treatment improved glucose metabolism via activation of the IR/IRS-2/PI3K/PKB/GSK-3 beta signaling pathway (which is related to glycogen synthesis) and enhanced glucose transport through insulin signaling cascade-induced GLUT4 translocation. Because of its effectiveness and stability, SRPC could be used as a therapeutic agent for blood glucose control and a promising nutraceutical for T2DM treatment.
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页数:9
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