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紫云英果寡糖:分子大小对其在高脂饮食和链脲佐菌素诱导糖尿病大鼠中抗糖尿病活性的影响。

Fructooligosaccharides from Cynoglossum tubiflorus: Effect of the molecular size on their antidiabetic activity in high-fat diet and alloxan induced diabetic rats.

机构信息

Laboratory of Organic Chemistry LR17ES08, Natural Substances Team, Faculty of Sciences of Sfax, University of Sfax, P.B.1171, Sfax 3000, Tunisia.

Laboratory of Organic Chemistry LR17ES08, Natural Substances Team, Faculty of Sciences of Sfax, University of Sfax, P.B.1171, Sfax 3000, Tunisia.

出版信息

Bioorg Chem. 2024 Feb;143:107100. doi: 10.1016/j.bioorg.2024.107100. Epub 2024 Jan 6.

Abstract

The use of acetylation followed by silica gel column purification allowed the isolation of eight fructooligosaccharides (FOS) from the ethanol extract of Cynoglossum tubiflorus roots. Each FOS was identified by analyzing its FT-IR, HRMS/MS and NMR data, including H, C and 2D NMR HH COSY, HMBC and NOESY. In diabetic rats treated with a series of FOS from Glc-(Fru) to Glc-(Fru), a significant inhibition of intestinal α-amylase was observed. This activity increases proportionally with the FOS molecular size. It was found that they delay the absorption of total cholesterol (TC), ldl-cholesterol (LDL-C) and increase HDL-cholesterol (HDL-C) in a molecular size-dependent manner. This inhibitory effect on the activity of the digestive enzyme causes a significant (p < 0.05) reduction in the level of glucose in the blood as an anti-diabetic action. The ethanolic extract (E.E) exerts a significant effect against α-amylase as well as antihyperglycemic and antihyperlipidemic actions, while its acetylation suppresses these effects. Therefore, this study demonstrates for the first time that pure FOS act as an efficient agent in preventing hyperglycemia and hyperlipidemia and that this action evolves in the same manner with their molecular size.

摘要

使用乙酰化反应和硅胶柱层析纯化,从白花菜科植物白花菜的乙醇提取物中分离得到了 8 种低聚果糖(FOS)。通过分析其傅里叶变换红外光谱(FT-IR)、高分辨质谱/质谱联用(HRMS/MS)和核磁共振(NMR)数据,包括氢谱(H)、碳谱(C)和二维核磁共振(2D NMR)HH COSY、HMBC 和 NOESY,对每种 FOS 进行了鉴定。在糖尿病大鼠中,用一系列从 Glc-(Fru)到 Glc-(Fru)的 FOS 进行治疗,观察到对肠道α-淀粉酶的显著抑制作用。这种活性与 FOS 的分子大小成正比增加。结果发现,它们以分子大小依赖的方式延迟了总胆固醇(TC)、低密度脂蛋白胆固醇(LDL-C)的吸收,并增加了高密度脂蛋白胆固醇(HDL-C)。这种对消化酶活性的抑制作用导致血糖水平显著(p<0.05)降低,从而起到抗糖尿病作用。乙醇提取物(E.E.)对α-淀粉酶以及降血糖和降血脂均有显著作用,而其乙酰化则抑制了这些作用。因此,本研究首次证明,纯 FOS 作为预防高血糖和高血脂的有效药物,其作用方式与其分子大小相同。

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