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Xinyu Wang, Han Ye, Jiefen Cui, Yongzhou Chi, Ruizhi Liu, Peng Wang. 2022: Hypolipidemic effect of chromium-modified enzymatic product of sulfated rhamnose polysaccharide from Enteromorpha prolifera in type 2 diabetic mice. Marine Life Science & Technology, 4(2): 245-254. DOI: 10.1007/s42995-022-00127-0
Citation: Xinyu Wang, Han Ye, Jiefen Cui, Yongzhou Chi, Ruizhi Liu, Peng Wang. 2022: Hypolipidemic effect of chromium-modified enzymatic product of sulfated rhamnose polysaccharide from Enteromorpha prolifera in type 2 diabetic mice. Marine Life Science & Technology, 4(2): 245-254. DOI: 10.1007/s42995-022-00127-0

Hypolipidemic effect of chromium-modified enzymatic product of sulfated rhamnose polysaccharide from Enteromorpha prolifera in type 2 diabetic mice

  • Sulfated rhamnose polysaccharide (SRP) derived from Enteromorpha prolifera is a metal-ion chelating agent that could potentially be used to treat diabetes. The aim of our study was to determine the effect of a variant of SRP on DIABETES. First, we synthesized and characterized SRPE-3 chromium(Ⅲ) SRPE-3-Cr(Ⅲ) complex using an enzymatic method. The maximum chelation rate was 18.2% under optimal chelating conditions of pH 6.0, time 4 h, and temperature 60 ℃. Fourier transform infrared spectroscopy results showed important sites for Cr(Ⅲ)-binding were O–H and C=O groups. We then studied the hypolipidemic effects of SRPE-3-Cr(Ⅲ) on type 2 diabetes mellitus (T2DM) induced by a high-fat, high-sucrose diet (HFSD). Decreased blood glucose content, body fat ratio, serum TG, TC, LDL-C, and increased serum HDL-C were observed after treatment with SRPE-3-Cr(Ⅲ). In addition, SRPE-3-Cr(Ⅲ) significantly reduced leptin, resistin, and TNF-α levels, and increased adiponectin contents relative to T2DM. Histopathology results also showed that SRPE-3-Cr(Ⅲ) could alleviate the HFSD-lesioned tissues. SRPE-3-Cr(Ⅲ) also improved lipid metabolism via a reduction in aspartate aminotransferase, alanine aminotransferase, fatty acid synthase, and acetyl-CoA carboxylase activities in the liver. SRPE-3-Cr(Ⅲ) at low doses exhibited better lipid-lowering activities, hence, could be considered to be a novel compound to treat hyperlipidemia and also act as an anti-diabetic agent.
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