Petalonia improves glucose homeostasis in streptozotocin-induced diabetic mice

被引:35
|
作者
Kang, Seong-Il [1 ]
Jin, Young-Jun [1 ]
Ko, Hee-Chul [2 ]
Choi, Soo-Youn [3 ]
Hwang, Joon-Ho [3 ]
Whang, Ilson [1 ]
Kim, Moo-Han [1 ]
Shin, Hye-Sun [1 ]
Jeong, Hyung-Bok [1 ]
Kim, Se-Jae [1 ]
机构
[1] Cheju Natl Univ, Dept Life Sci, Jejusi 690756, Jeju, South Korea
[2] Cheju Natl Univ, Dept Chem, Jejusi 690756, Jeju, South Korea
[3] Cheju Natl Univ, Reg Innovat Ctr, Jejusi 690756, Jeju, South Korea
关键词
Petalonia binghamiae; seaweed; 3T3-L1; cells; adipocyte differentiation; PPAR gamma; streptozotocin-induced diabetic mice; insulin;
D O I
10.1016/j.bbrc.2008.06.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The anti-diabetic potential of Petalonia binghamiae extract (PBE) was evaluated in vivo. Dietary administration of PBE to streptozotocin (STZ)-induced diabetic mice significantly lowered blood glucose levels and improved glucose tolerance. The mode of action by which PBE attenuated diabetes was investigated in vitro using 3T3-L1 cells. PBE treatment stimulated 3T3-L1 adipocyte differentiation as evidenced by increased triglyceride accumulation. At the molecular level, peroxisome proliferator-activated receptor gamma (PPAR gamma) and terminal marker protein aP2, as well as the mRNA of GLUT4 were up-regulated by PBE. In mature adipocytes, PBE significantly stimulated the uptake of glucose and the expression of insulin receptor substrate-1 (IRS-1). Furthermore, PBE increased PPAR gamma luciferase reporter gene activity in COS-1 cells. Taken together, these results suggest that the in vivo anti-diabetic effect of PBE is mediated by both insulin-like and insulin-sensitizing actions in adipocytes. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:265 / 269
页数:5
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