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香菇(Lentinula edodes (Berk.) Pegler)中高分子量可溶性膳食纤维的结构特征及其与胰脂肪酶和胆汁盐的相互作用机制。

Structure characterization of high molecular weight soluble dietary fiber from mushroom Lentinula edodes (Berk.) Pegler and its interaction mechanism with pancreatic lipase and bile salts.

机构信息

Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin 300072, PR China.

Tianjin Agricultural University, Tianjin 300384, PR China; State Key Laboratory of Nutrition and Safety, Tianjin University of Science & Technology, Tianjin 300457, PR China.

出版信息

Int J Biol Macromol. 2020 Jun 15;153:1281-1290. doi: 10.1016/j.ijbiomac.2019.10.263. Epub 2019 Nov 20.

Abstract

Aimed to evaluate the hypolipidemic effects of high molecular weight soluble dietary fiber extracted from L. edodes (LEHSDF), this study investigated the structure and interaction mechanism of LEHSDF with pancreatic lipase (PL) and bile salts (BS) that were involved in lipid digestion. 1D/2D NMR spectra indicated that the main chain of LEHSDF consisted of (1 → 2,4)-linked β-D-arabinopyranosyl, (1 → 3)-linked α-L-rhamnopyranosyl, (1 → 4)-linked β-D-xylopyranosyl, (1 → 6)-linked and (1 → 4)-linked β-D-glucopyranosyl, with β-D-galactopyranosyl and α-D-mannopyranosyl as terminal unit. Oil red O staining results suggested that LEHSDF had an effective inhibitory effect on lipid accumulation in HepG2 cells. Isothermal titration calorimetry, fluorescence and circular dichroism spectra showed that BS did not specifically bind to LEHSDF, and the strong inhibitory effect of LEHSDF on lipase was dominated by hydrophobic forces, electrostatic forces, encapsulation and adsorption interactions. The results will be helpful for the design of food containing LEHSDF as a functional additive to control lipid digestion.

摘要

本研究旨在评估从香菇(LEHSDF)中提取的高分子量可溶性膳食纤维的降血脂作用,研究了 LEHSDF 与参与脂质消化的胰脂肪酶(PL)和胆汁盐(BS)的结构和相互作用机制。1D/2D NMR 谱表明,LEHSDF 的主链由(1→2,4)-连接的β-D-阿拉伯吡喃糖基、(1→3)-连接的α-L-鼠李吡喃糖基、(1→4)-连接的β-D-木吡喃糖基、(1→6)-连接的和(1→4)-连接的β-D-吡喃葡萄糖基组成,以β-D-吡喃半乳糖基和α-D-吡喃甘露糖基为末端单元。油红 O 染色结果表明,LEHSDF 对 HepG2 细胞的脂质积累具有有效抑制作用。等温滴定量热法、荧光和圆二色光谱表明,BS 与 LEHSDF 没有特异性结合,LEHSDF 对脂肪酶的强烈抑制作用主要由疏水作用力、静电力、包合和吸附相互作用主导。这些结果将有助于设计含有 LEHSDF 的食品作为控制脂质消化的功能性添加剂。

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