Phosphatidylinositol-3-kinase is involved in the antihyperglycemic effect induced by resveratrol in streptozotocin-induced diabetic rats

被引:140
作者
Chi, Tzong-Cherng
Chen, Win-Pin
Chi, Tsung-Li
Kuo, Tzong-Fu
Lee, Shoei-Sheng
Cheng, Juei-Tang
Su, Ming-Jai
机构
[1] Natl Taiwan Univ, Coll Med, Inst Pharmacol, Taipei 10764, Taiwan
[2] Natl Taiwan Univ, Coll Med, Sch Pharm, Taipei 10764, Taiwan
[3] Natl Kaohsiung First Univ Sci & Technol, Inst Program Management, Kaohsiung, Taiwan
[4] Natl Taiwan Univ, Grad Inst Vet Med, Taipei 10764, Taiwan
[5] Natl Cheng Kung Univ, Coll Med, Dept Pharmacol, Tainan 70101, Taiwan
关键词
resveratrol; IDDM; NIDDM; Akt phosphorylation; glucose transporter subtype 4; phosphoenolpyruvate carboxykinase;
D O I
10.1016/j.lfs.2007.02.002
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Resveratrol, a polyphenolic substance found in grape skin, is proposed to account in part for the protective effect of red wine in the cardiovascular system. The aim of the present study is to investigate the action and possible mechanisms of resveratrol-produced regulation of plasma glucose in normal and diabetic rats including the animal model of streptozotocin (STZ)-induced and nicotinamide-STZ-induced (NASTZ), and insulin-resistant diabetic rats. Resveratrol (p.o.) produced a hypoglycernic effect in a dose-dependent manner in normal and diabetic rats, and the insulin level was increased following resveratrol treatment in normal and NA-STZ diabetic rats. In insulin-deficient STZ-diabetic rats, resveratrol significantly lowered the plasma glucose 90 min after oral treatment, and the hypoglycernic effect was abolished by phosphatidyl-3-kinase (PI3K) inhibitors (LY294002 and wortmannin) which also inhibited resveratrol-induced Akt phosphorylation in soleus muscle of STZ-diabetic rats. The change in the protein expression level of glucose transporter subtype 4 (GLUT4) in the soleus muscle and phosphoenolpyruvate carboxykinase (PEPCK) in the liver of STZ-diabetic rats treated with resveratrol (3 mg/kg, p.o.) for 7 days was examined. Resveratrol normalized hepatic PEPCK expression and increased GLUT4 expression in the soleus muscle of STZ-diabetic rats. The results indicate that the mechanisms contributing to the hypoglycemic effect of resveratrol include insulin-dependent and insulin-independent pathway, and PI3K-Akt-signaling was involved in the latter mechanism to enhance glucose uptake in skeletal muscle. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1713 / 1720
页数:8
相关论文
共 29 条
[1]  
Aggarwal BB, 2004, ANTICANCER RES, V24, P2783
[2]   Antidiabetic activity of red wine polyphenolic extract, ethanol, or both in streptozotocin-treated rats [J].
Al-Awwadi, N ;
Azay, J ;
Poucheret, P ;
Cassanas, G ;
Krosniak, M ;
Auger, C ;
Gasc, F ;
Rouanet, JM ;
Cros, G ;
Teissèdre, PL .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2004, 52 (04) :1008-1016
[3]   DECREASED EXPRESSION OF THE INSULIN-RESPONSIVE GLUCOSE TRANSPORTER IN DIABETES AND FASTING [J].
BERGER, J ;
BISWAS, C ;
VICARIO, PP ;
STROUT, HV ;
SAPERSTEIN, R ;
PILCH, PF .
NATURE, 1989, 340 (6228) :70-72
[4]   Protein kinase B phosphorylation of PIKfyve regulates the trafficking of GLUT4 vesicles [J].
Berwick, DC ;
Dell, GC ;
Welsh, GI ;
Heesom, KJ ;
Hers, I ;
Fletcher, LM ;
Cooke, FT ;
Tavaré, JM .
JOURNAL OF CELL SCIENCE, 2004, 117 (25) :5985-5993
[5]   The role of carbohydrates in insulin resistance [J].
Bessesen, DH .
JOURNAL OF NUTRITION, 2001, 131 (10) :2782S-2786S
[6]   Antihyperglycemic action of angiotensin II receptor antagonist, valsartan, in streptozotocin-induced diabetic rats [J].
Chan, P ;
Wong, KL ;
Liu, IM ;
Tzeng, TF ;
Yang, TL ;
Cheng, JT .
JOURNAL OF HYPERTENSION, 2003, 21 (04) :761-769
[7]  
Chang Chi, 1936, Information Bulletin, V1, P1
[8]   Plasma glucose-lowering effect of tramadol in streptozotocin-induced diabetic rats [J].
Cheng, JT ;
Liu, IM ;
Chi, TC ;
Tzeng, TF ;
Lu, FH ;
Chang, CJ .
DIABETES, 2001, 50 (12) :2815-2821
[9]  
Chi Tzong-Cherng, 1998, Chinese Pharmaceutical Journal (Taipei), V50, P113
[10]   Resveratrol-mediated activation of cAMP response element-binding protein through adenosine A3 receptor by Akt-dependent and -independent pathways [J].
Das, S ;
Tosaki, A ;
Bagchi, D ;
Maulik, N ;
Das, DK .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2005, 314 (02) :762-769