SGLT2 Inhibitors and Its Role in Diabetes

G. Himabindhu
{"title":"SGLT2 Inhibitors and Its Role in Diabetes","authors":"G. Himabindhu","doi":"10.35248/2161-1017.20.9.313","DOIUrl":null,"url":null,"abstract":"SGLT2 is a low-affinity, and high capacity glucose transporter located in the kidneys (proximal tubule). It is responsible for 90% of glucose reabsorption. Inhibition of SGLT2 leads to decrease in blood glucose due to increase in renal glucose excretion. The mechanism of action of this newest class of drugs also offers further glucose control by allowing increased insulin sensitivity and uptake of glucose in the muscle cells, decreased gluconeogenesis and improved first phase insulin release from the beta cells.","PeriodicalId":11670,"journal":{"name":"Endocrinology and Metabolic Syndrome","volume":"50 1","pages":"1-1"},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Endocrinology and Metabolic Syndrome","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.35248/2161-1017.20.9.313","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

SGLT2 is a low-affinity, and high capacity glucose transporter located in the kidneys (proximal tubule). It is responsible for 90% of glucose reabsorption. Inhibition of SGLT2 leads to decrease in blood glucose due to increase in renal glucose excretion. The mechanism of action of this newest class of drugs also offers further glucose control by allowing increased insulin sensitivity and uptake of glucose in the muscle cells, decreased gluconeogenesis and improved first phase insulin release from the beta cells.
SGLT2抑制剂及其在糖尿病中的作用
SGLT2是一种低亲和力、高容量的葡萄糖转运蛋白,位于肾脏(近端小管)。它负责90%的葡萄糖再吸收。抑制SGLT2导致血糖降低,这是由于肾脏葡萄糖排泄增加所致。这类最新药物的作用机制还通过增加胰岛素敏感性和肌肉细胞对葡萄糖的摄取,减少糖异生和改善β细胞的第一阶段胰岛素释放来进一步控制葡萄糖。
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