Antidiabetic effect of total saponins from Polygonatum kingianum in streptozotocin-induced daibetic rats

被引:62
作者
Lu, Jian-mei [1 ,2 ]
Wang, Yan-fang [1 ,2 ]
Yan, Hong-li [1 ,2 ]
Lin, Pei [1 ,2 ]
Gu, Wen [1 ,2 ]
Yu, Jie [1 ,2 ]
机构
[1] Yunnan Univ Tradit Chinese Med, Kunming 650500, Peoples R China
[2] Yunnan Univ Tradit Chinese Med, Dept Pharm, 1076 Yuhua Rd, Kunming, Yunnan Province, Peoples R China
基金
中国国家自然科学基金;
关键词
Total saponins; Polygonatum kingianum; Antidiabetic effect; Insulin signaling pathway; INSULIN-RESISTANCE; STEROIDAL SAPONINS; FRESH RHIZOMES; ODORATUM; PATHWAY;
D O I
10.1016/j.jep.2015.12.057
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Polygonatum kingianum has been used in the prevention and treatment of diabetes, hyperlipidemia and related metabolic syndrome in Asian counties for centuries. In this study, the blood glucose regulation activity and mechanism of total saponins from P. kingianum (TSPK) were investigated in streptozotocin (STZ)-induced diabetic rats in this research. Methods: TSPK (0.025 g/kg and 0.1 mg/kg) was administrated by gavage to STZ-induced diabetic rats for 8 weeks. Changes of body weight, food intakes, blood glucose, serum insulin and lipid indexes were observed. Genome-wide expression profiling was applied to explore the gene expression alternation after treated with TSPK. Expressions of adenosine monophosphate activated protein kinase (AMPK), phosphoenolpyruvate carboxykinase (PEPCK), the relative transcript level of glucose kinase and glucose-6-phosphatase (GK/G6P) in the liver were investigated. Meanwhile, contents of AMPK, and glucose transporter subtype-4 (GLUT4) in skeletal muscle, and peroxysome proliferator-activated receptor (PPAR-gamma) in adipose tissue were investigated. Results: TSPK could effectively alleviate hyperglycemia and hyperlipidemia in diabetic rats. Genome-wide expression profiling showed that TSPK up-regulated the expression of GLUT4 while down-regulated the expression of G6P in insulin signal pathway. In the liver, the expression of AMPK and GK are increased. Further more, TSPK promoted the expressions of GLUT4 in skeletal muscle, and PPAR-gamma in adipose tissue, respectively. Conclusion: These results provide possible mechanisms for the antidiabetic effects of TSPK. TSPK could promote not only glycogenesis but also glucose utilization in peripheral tissue. Our results suggested that TSPK may be used as adjuvant therapy to control blood glucose and insulin resistance in type 2 diabetic individuals. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:291 / 300
页数:10
相关论文
共 40 条
[1]   Hypoglycemic effects of aqueous extract of Rhizoma Polygonati Odorati in mice and rats [J].
Chen, HB ;
Feng, RZ ;
Guo, Y ;
Sun, LH ;
Jiang, JL .
JOURNAL OF ETHNOPHARMACOLOGY, 2001, 74 (03) :225-229
[2]   A steroidal glycoside from Polygonatum odoratum (Mill.) Druce. improves insulin resistance but does not alter insulin secretion in 90% pancreatectomized rats [J].
Choi, SB ;
Park, S .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2002, 66 (10) :2036-2043
[3]  
Commission of China Flora, 1978, FLORA CHINA, V15, P64
[4]  
Commission of Chinese Materia Medica, 1999, CHINESE MAT MED, V8, P8142
[5]  
Commission of Chinese Medicine Dictionary, 2006, CHIN MED DICT 2, P2828
[6]  
Commission of Chinese Pharmacopoeia, 2015, PHARMACOPOEIA PEOPLE, V288, P857
[7]   Saponin rich fractions from Polygonatum odoratum (Mill.) Druce with more potential hypoglycemic effects [J].
Deng, Yafei ;
He, Kai ;
Ye, Xiaoli ;
Chen, Xin ;
Huang, Jing ;
Li, Xuegang ;
Yuan, Lujiang ;
Jin, Yalan ;
Jin, Qing ;
Li, Panpan .
JOURNAL OF ETHNOPHARMACOLOGY, 2012, 141 (01) :228-233
[8]   Prostaglandins and fatty acids regulate transcriptional signaling via the peroxisome proliferator activated receptor nuclear receptors [J].
Dussault, I ;
Forman, BM .
PROSTAGLANDINS & OTHER LIPID MEDIATORS, 2000, 62 (01) :1-13
[9]   MECHANISMS OF DIABETIC COMPLICATIONS [J].
Forbes, Josephine M. ;
Cooper, Mark E. .
PHYSIOLOGICAL REVIEWS, 2013, 93 (01) :137-188
[10]   Extracts of Rhizoma Polygonati Odorati Prevent High-Fat Diet-Induced Metabolic Disorders in C57BL/6 Mice [J].
Gu, Ming ;
Zhang, Yu ;
Fan, Shengjie ;
Ding, Xiaobo ;
Ji, Guang ;
Huang, Cheng .
PLOS ONE, 2013, 8 (11)