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二肽基肽酶-Ⅳ抑制剂的降糖机制研究进展

王结胜

中国医学科学院学报2013,Vol.35Issue(2):229-233,5.
中国医学科学院学报2013,Vol.35Issue(2):229-233,5.DOI:10.3881/j.issn.1000-503X.2013.02.019

二肽基肽酶-Ⅳ抑制剂的降糖机制研究进展

Research Progress of Mechanisms through which Dipeptidyl Peptidase-Ⅳ Inhibitors Regulate Glycemia

王结胜1

作者信息

  • 1. 浙江省立同德医院干部保健科,杭州,310012
  • 折叠

摘要

Abstract

Corresponding author; WANG Jie-sheng Tel: 0571-89972437, E-mail: wwjjss2000@163. com Dipeptidyl peptidase-Ⅳ (DPP-Ⅳ) inhibitors are promising new antidiabetic drugs. It had been proposed that DPP-Ⅳ inhibitors exert their antidiabetic effect by inhibiting the degradation of glucagon-like peptide 1 (GLP-1) . However, new evidence has shown that the increase of GLP-1 is not notable after the use of these drugs in patients with type 2 diabetes. Therefore, the specific mechanisms via which DPP-Ⅳ inhibitors in controlling blood glucose has became questionable. In recent years, studies have revealed many possible mechanisms through which DPP-Ⅳ inhibitors regulate glycemia: DPP-Ⅳ inhibitors may selectively reduce DPP-Ⅳ activity in the intestine, causing the increase of portal plasma GLP-1 level and thus promoting the release of insulin via nerve reflex; also, they may decrease the cleavage product of GLP-1 and reduce the degradation of other bioactive peptides.

关键词

胰高血糖素样肽-1/二肽基肽酶-Ⅳ/血糖调节

Key words

glucagon-like peptide 1/ dipeptidyl peptidase-IV/ regulate glycemia

分类

医药卫生

引用本文复制引用

王结胜..二肽基肽酶-Ⅳ抑制剂的降糖机制研究进展[J].中国医学科学院学报,2013,35(2):229-233,5.

中国医学科学院学报

OA北大核心CSCDCSTPCDMEDLINE

1000-503X

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