Lee Yeong-Eun, Yoo So-Hee, Chung Jin-Oh, Park Mi-Young, Hong Yong-Deog, Park Si-Hyun, Park Tae-Sik, Shim Soon-Mi
Department of Food Science and Technology, Sejong University, Seoul, Republic of Korea.
AMOREPACIFIC R&D Center, 1920, Youngu-daero, Giheung-gu, Yongin-si, Gyeonggi-do, Republic of Korea.
J Sci Food Agric. 2020 Aug;100(10):3979-3986. doi: 10.1002/jsfa.10442. Epub 2020 May 28.
Water soluble polysaccharide derived from green tea (WSP) is produced as byproducts when catechins were extracted from green tea. Although inhibitory effect of green tea catechins on the glucose transport in small intestine has been studied, the hypoglycemic efficacy of the WSP or its combinational effect has not been studied. In order to investigate hypoglycemic efficacy of the WSP or its combinational effect with green tea extract (GTE), co-consumption of GTE and WSP with wheat starch was investigated using in vitro digestion coupled with Caco-2 cells. The mechanism of the intestinal glucose transport was elucidated throughout the gene expression of the intestinal glucose transporters, which included sodium dependent glucose transporter (SGLT1) and glucose transporter 2 (GLUT2), using quantitative real-time polymerase chain reaction (qRT-PCR).
The co-digestion of wheat starch with GTE during the small intestinal phase was the most rapidly digested into reducing sugar (73.96 g L ) compared to itself (48.44 g L ), WSP (60.35 g L ), and GTE + WSP (61.81 g L ). Intestinal glucose transport was 11.82, 7.59, 4.49, and 2.40% for wheat starch, wheat starch with GTE, WSP, and GTE + WSP, respectively. The highest decreased expression pattern in SGLT1 was observed when cells treated with wheat starch + GTE + WSP (0.66-fold) compared to GTE or WSP treatment.
The results suggested that co-consumption of green tea derived products with wheat starch could delay the intestinal absorption of glucose. Results from the current study suggested that GTE and WSP could be the useful supplements of dietary therapy for hyperglycemia to delay glucose absorption. © 2020 Society of Chemical Industry.
从绿茶中提取儿茶素时会产生水溶性多糖(WSP)作为副产品。虽然绿茶儿茶素对小肠葡萄糖转运的抑制作用已被研究,但WSP的降血糖功效或其联合作用尚未得到研究。为了研究WSP的降血糖功效或其与绿茶提取物(GTE)的联合作用,采用体外消化结合Caco-2细胞的方法,研究了GTE和WSP与小麦淀粉共同食用的情况。通过定量实时聚合酶链反应(qRT-PCR),从肠道葡萄糖转运蛋白的基因表达方面阐明了肠道葡萄糖转运的机制,这些转运蛋白包括钠依赖性葡萄糖转运蛋白(SGLT1)和葡萄糖转运蛋白2(GLUT2)。
与小麦淀粉自身(48.44 g/L)、WSP(60.35 g/L)和GTE+WSP(61.81 g/L)相比,在小肠阶段小麦淀粉与GTE共同消化时,还原糖的消化速度最快(73.96 g/L)。小麦淀粉、小麦淀粉与GTE、WSP以及GTE+WSP的肠道葡萄糖转运率分别为11.82%、7.59%、4.49%和2.40%。与GTE或WSP处理相比,当细胞用小麦淀粉+GTE+WSP处理时,SGLT1的表达下降模式最为明显(0.66倍)。
结果表明,绿茶衍生产品与小麦淀粉共同食用可延缓肠道对葡萄糖的吸收。本研究结果表明,GTE和WSP可能是高血糖饮食治疗中延缓葡萄糖吸收的有用补充剂。©2020化学工业协会。