Search for Compounds Suppressing Intestinal α-Glucosidase Expression in Caco-2 Cells

K. Noda, E. Kato, J. Kawabata
{"title":"Search for Compounds Suppressing Intestinal α-Glucosidase Expression in Caco-2 Cells","authors":"K. Noda, E. Kato, J. Kawabata","doi":"10.33555/iconiet.v2i2.18","DOIUrl":null,"url":null,"abstract":"Diabetes is a chronic disease characterized by elevated blood glucose level.Reducing carbohydrate absorption from the intestinal tract is an effective strategy to control post-meal blood glucose level. Inhibition of intestinal α-glucosidase, involved in digestion of carbohydrates, is known as an approach to accomplish this. On the other hand, reduction of α-glucosidase amount is expected to work in the similar manner. However, none of the previousstudy pursues this approach. A convenient assay was developed to evaluate α-glucosidase amount employing Caco-2 cells, the intestinal epithelial cell model reported to express α-glucosidase. Sixty plants were screened and two candidate plants, Calluna vulgaris and Perilla frutescens var. crispa were found to reduce α-glucosidase expression. C. vulgaris extract was subjected to activity guided isolation. Proanthocyanidin was identified as the active principle which was analyzed by thiol decomposition to reveal the components as a mixture ofcatechin, epicatechin, epigallocatechin, and A type procyanidin dimer. The proanthocyanidin suppressed about 30% of α-glucosidase amount evaluated through convenient assay, and suppressed bulk of mRNA expression level of sucrase-isomaltase (SI) at 0.125 mg/mL. Several flavan-3-ol monomers were also tested, and epicatechin gallate and epigallocatechin gallate were found to suppress α-glucosidase amount significantly.","PeriodicalId":13150,"journal":{"name":"ICONIET PROCEEDING","volume":"10 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ICONIET PROCEEDING","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33555/iconiet.v2i2.18","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Diabetes is a chronic disease characterized by elevated blood glucose level.Reducing carbohydrate absorption from the intestinal tract is an effective strategy to control post-meal blood glucose level. Inhibition of intestinal α-glucosidase, involved in digestion of carbohydrates, is known as an approach to accomplish this. On the other hand, reduction of α-glucosidase amount is expected to work in the similar manner. However, none of the previousstudy pursues this approach. A convenient assay was developed to evaluate α-glucosidase amount employing Caco-2 cells, the intestinal epithelial cell model reported to express α-glucosidase. Sixty plants were screened and two candidate plants, Calluna vulgaris and Perilla frutescens var. crispa were found to reduce α-glucosidase expression. C. vulgaris extract was subjected to activity guided isolation. Proanthocyanidin was identified as the active principle which was analyzed by thiol decomposition to reveal the components as a mixture ofcatechin, epicatechin, epigallocatechin, and A type procyanidin dimer. The proanthocyanidin suppressed about 30% of α-glucosidase amount evaluated through convenient assay, and suppressed bulk of mRNA expression level of sucrase-isomaltase (SI) at 0.125 mg/mL. Several flavan-3-ol monomers were also tested, and epicatechin gallate and epigallocatechin gallate were found to suppress α-glucosidase amount significantly.
在Caco-2细胞中寻找抑制肠道α-葡萄糖苷酶表达的化合物
糖尿病是一种以血糖升高为特征的慢性疾病。减少肠道碳水化合物的吸收是控制餐后血糖水平的有效策略。抑制参与碳水化合物消化的肠道α-葡萄糖苷酶被认为是实现这一目标的一种方法。另一方面,α-葡萄糖苷酶量的减少预计也以类似的方式起作用。然而,之前的研究都没有采用这种方法。建立了以Caco-2细胞(已报道表达α-葡萄糖苷酶的肠上皮细胞模型)评价α-葡萄糖苷酶含量的简便方法。对60株植物进行筛选,发现愈伤组织和紫苏(Perilla frutescens var. crispa)两种候选植物可降低α-葡萄糖苷酶的表达。采用活性引导分离方法分离荆芥提取物。经硫醇分解分析,其活性成分为儿茶素、表儿茶素、没食子儿茶素和a型原花青素二聚体的混合物。原花青素对α-葡萄糖苷酶的抑制作用约为30%,在0.125 mg/mL时抑制了蔗糖-异麦芽糖酶(SI) mRNA的表达量。几种黄烷-3-醇单体也进行了测试,发现表儿茶素没食子酸酯和表没食子儿茶素没食子酸酯能显著抑制α-葡萄糖苷酶的数量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信