Thiazolidinediones (TZDs) enhance insulin secretory response via GPR40 and adenylate cyclase (AC)

被引:5
作者
Hwang, Mina [1 ]
Kim, Hyo-Sup [1 ]
Jin, Sang-Man [2 ]
Hur, Kyoo-Yeon [2 ]
Kim, Jae-Hyeon [2 ]
Lee, Moon-Kyu [3 ]
机构
[1] Sungkyunkwan Univ, Samsung Biomed Res Inst, Div Endocrinol & Metab, Samsung Med Ctr,Sch Med, Seoul, South Korea
[2] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Endocrinol & Metab, Seoul, South Korea
[3] Eulji Univ, Eulji Univ Hosp, Dept Internal Med, Div Endocrinol & Metab,Uijeongbu Med Ctr, Uijongbu, South Korea
关键词
adenylyl cyclase; cAMP; glucolipotoxicity; GPR40; insulin secretion; lobeglitazone; ACTIVATED RECEPTOR-GAMMA; PANCREATIC BETA-CELLS; FREE FATTY-ACIDS; PEROXISOME PROLIFERATOR; PPAR-GAMMA; GENE; GLUCOSE; CAMP; METABOLISM; EXPRESSION;
D O I
10.1002/jcp.30467
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Thiazolidinediones are synthetic PPAR gamma ligands that enhance insulin sensitivity, and that could increase insulin secretion from beta-cells. However, the functional role and mechanism(s) of action in pancreatic beta-cells have not been investigated in detail.
引用
收藏
页码:8137 / 8147
页数:11
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