游离脂肪酸受体1
兴奋剂
激活剂(遗传学)
内分泌学
糖尿病
胰岛素
药理学
药品
化学
内科学
医学
受体
作者
Hiroshi Kamiyama,Yasuo Terauchi
出处
期刊:PubMed
[National Institutes of Health]
日期:2015-03-01
卷期号:73 (3): 517-22
被引量:3
摘要
Clinical development of novel antidiabetic drugs, such as GK activator, GPR40 agonist, GPR119 agonist, 11β-HSD1 inhibitor and trelagliptin, has been progressing over the world. Especially, GK activator, GPR40 agonist, GPR119 agonist and 112-HSD1 inhibitor have unique action mechanism compared to existing drugs. GK activator potentiates glucose-stimulated insulin secretion from β cells and stimulates glucose uptake into the liver. GPR40 agonists and GPR119 agonist stimulate glucose-dependent insulin secretion from β cells. 11β-HSD1 inhibitor reduces the conversion of cortisone to cortisol. Trelagliptin is a long acting dipeptidyl peptidase-4(DPP-4) inhibitor and a once-weekly treatment by trelagliptin would improve the drug adherence of patients. This article focuses on these new and emerging diabetes agents.
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