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微生物葡聚糖在小肠α-葡萄糖苷酶水平下的缓慢水解特性导致小鼠模型中的血糖反应得到调节。

Slowly hydrolyzable property of microbial dextrans at the small intestinal α-glucosidase levels leads to the modulated glycemic responses in the mouse model.

作者信息

Bae Dain, Song Young-Bo, Choi Hyunwook, Lee Byung-Hoo

机构信息

Department of Food Science and Biotechnology, Gachon University, Seongnam 13120, Republic of Korea.

Department of Food and Nutrition, Jeonju University, Jeonju 55069, Republic of Korea.

出版信息

Int J Biol Macromol. 2024 Oct;277(Pt 2):134322. doi: 10.1016/j.ijbiomac.2024.134322. Epub 2024 Jul 31.

Abstract

Dextran-type α-glucans have been known as non-digestible ingredients that can be considered prebiotics to promote colon health. However, recent studies have revealed that various α-linked glucosyl units are hydrolyzed to glucose by small intestinal α-glucosidases. This study analyzed the structural characteristics of exopolysaccharides (EPSs) from Weissella species, and the hydrolysis properties at both in vitro/in vivo levels were investigated. Compared with a previous in vitro digestion model using fungal α-hydrolytic enzymes, dextrans, which mainly consist of α-1,6 linkages with small amounts of α-1,3 linked glucose units, were slowly hydrolyzed to glucose by mammalian mucosal α-glucosidases, resulting in attenuation of the initial glycemic response following administration of EPS samples to mice via oral gavage. The results of this study demonstrate the concept of dextran-type α-glucans as glycemic carbohydrates rather than dietary fibers or prebiotics. Slowly digestible dextrans can be applied as a functional ingredient to regulate postprandial glucose delivery throughout the gastrointestinal tract.

摘要

葡聚糖型α-葡聚糖一直被认为是不可消化的成分,可被视为促进结肠健康的益生元。然而,最近的研究表明,各种α-连接的葡萄糖基单元会被小肠α-葡萄糖苷酶水解为葡萄糖。本研究分析了魏斯氏菌属胞外多糖(EPS)的结构特征,并研究了其在体外/体内水平的水解特性。与之前使用真菌α-水解酶的体外消化模型相比,主要由α-1,6连接和少量α-1,3连接的葡萄糖单元组成的葡聚糖,被哺乳动物黏膜α-葡萄糖苷酶缓慢水解为葡萄糖,导致通过口服灌胃给小鼠施用EPS样品后,初始血糖反应减弱。本研究结果证明了葡聚糖型α-葡聚糖作为血糖碳水化合物而非膳食纤维或益生元的概念。缓慢消化的葡聚糖可作为功能性成分应用于调节整个胃肠道的餐后葡萄糖输送。

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