Improvement of myocardial glycolipid metabolic disorder in diabetic hamster with Astragalus polysaccharides treatment

被引:36
作者
Chen, Wei [2 ]
Xia, Yan-Ping [2 ]
Chen, Wen-Jie [2 ]
Yu, Mao-Hua [2 ]
Li, Yi-Ming [1 ]
Ye, Hong-Ying [1 ]
机构
[1] Fudan Univ, Dept Endocrinol, Huashan Hosp, Sch Med, Shanghai 200040, Peoples R China
[2] Fudan Univ, Dept Geriatr, Huashan Hosp, Sch Med, Shanghai 200040, Peoples R China
关键词
Diabetes; Cardiomyopathy; Astragalus polysaccharides; Glycolipid metabolism; PPAR-ALPHA; GLUT4; MICE;
D O I
10.1007/s11033-012-1595-y
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 objective of the present study is to observe the effect of Astragalus polysaccharide (APS) on myocardial glucose and lipid metabolism in diabetes (DM) hamster and to explore its mechanism in intervention of DM cardiomyopathy. Low-dose- streptozotocin-induced hamsters (STZ, 40 mg/kg x 3 days, i.p.) with blood glucose > 13.9 mmo/L were considered as type 2 diabetic models. We measure blood glucose, serum lipid, insulin, C-peptide, myocardial enzyme levels, myocardial glycogen staining, myocardial ultrastructure, fluorescence quantitative RT-PCR detection of myocardial PPAR-alpha and the target genes (FATP, ACS) and GLUT4 mRNA expression in normal control group, DM group and APS treatment group hamsters. There was significant glycolipid metabolic disorders in DM group compared with normal group. Glucose, glycosylated serum protein, myocardial enzymes and lipid levels in APS treatment group decreased significantly than DM group, but insulin and C-peptide levels was no difference. Myocardial glycogen staining and abnormal myocardial ultrastructure in APS treatment group were significantly improved than in DM group. Gene expression of myocardial PPAR-alpha and its target genes (FATP, ACS) in APS group were significantly lower than in DM group, while gene expression of GLUT4 in APS group was higher than DM group. APS can partially improve myocardial glucose and lipid metabolism disorders in diabetic hamsters and protect myocardium in some extent.
引用
收藏
页码:7609 / 7615
页数:7
相关论文
共 11 条
[1]   Astragalus polysaccharides: An effective treatment for diabetes prevention in NOD mice [J].
Chen, W. ;
Li, Y. -M. ;
Yu, M. -H. .
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 2008, 116 (08) :468-474
[2]  
Chen W, 2009, ACTA DIABETOL S1, V47, P535
[3]   Effects of astragalus polysaccharides on chymase, angiotensin-converting enzyme and angiotensin II in diabetic cardiomyopathy in hamsters [J].
Chen, Wei ;
Li, Yi-Ming ;
Yu, Mao-Hua .
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 2007, 35 (06) :873-877
[4]   Astragalus polysaccharides inhibited diabetic cardiomyopathy in hamsters depending on suppression of heart chymase activation [J].
Chen, Wei ;
Li, Yi-Ming ;
Yu, Mao-Hua .
JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2010, 24 (03) :199-208
[5]   Central role of PPARα-dependent hepatic lipid turnover in dietary steatohepatitis in mice [J].
Ip, E ;
Farrell, GC ;
Robertson, G ;
Hall, P ;
Kirsch, R ;
Leclercq, I .
HEPATOLOGY, 2003, 38 (01) :123-132
[6]  
Laukkanen J, 2002, EXP NEPHROL, V10, P150
[7]   Requirement of PPARα in maintaining phospholipid and triacylglycerol homeostasis during energy deprivation [J].
Lee, SST ;
Chan, WY ;
Lo, CKC ;
Wan, DCC ;
Tsang, DSC ;
Cheung, WT .
JOURNAL OF LIPID RESEARCH, 2004, 45 (11) :2025-2037
[8]   Vanadium increases GLUT4 in diabetic rat skeletal muscle [J].
Mohammad, A ;
Sharma, V ;
McNeill, JH .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2002, 233 (1-2) :139-143
[9]  
Suden MC, 2002, BIOCHEM J, V364, P361
[10]   Identification of a novel peroxisome proliferator-activated receptor (PPAR) γ promoter in man and transactivation by the nuclear receptor RORα1 [J].
Sundvold, H ;
Lien, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 287 (02) :383-390