Quercitrin, a bioflavonoid improves glucose homeostasis in streptozotocin-induced diabetic tissues by altering glycolytic and gluconeogenic enzymes

被引:55
作者
Babujanarthanam, Ranganathan [2 ]
Kavitha, Purushothaman [2 ]
Pandian, Moses Rajasekara [1 ]
机构
[1] Arignar Anna Govt Arts Coll, Dept Zool, Namakkal 637001, Tamil Nadu, India
[2] KMG Coll Arts & Sci, Dept Biochem, Gudiyatham 632602, Tamil Nadu, India
关键词
antioxidants; diabetes mellitus; gluconeogenesis; pancreas; quercitrin; streptozotocin; BETA-CELL; CARBOHYDRATE-METABOLISM; MESSENGER-RNA; RAT ISLETS; FLAVONOIDS; QUERCETIN; LIVER; ANTIOXIDANT; GLUCOSE-6-PHOSPHATASE; EXTRACT;
D O I
10.1111/j.1472-8206.2009.00771.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The present study is an investigation into the role of quercitrin on carbohydrate metabolism in normal and streptozotocin (STZ)-induced diabetic rats. Administration of STZ leads to a significant increase (P < 0.05) in fasting plasma glucose and a decrease in insulin levels. The content of glycogen is significantly decreased (P < 0.05) in liver and muscle, but increased in the kidney. The activity of hexokinase decreased whereas the activities of glucose 6-phosphatase and fructose 1,6-bisphosphatase significantly increased (P < 0.05) in the tissues. Oral administration of quercitrin (30 mg/kg) to diabetic rats for a period of 30 days resulted in significant (P < 0.05) alterations in the parameters studied but not in normal rats. A decrease of plasma glucose and increase in insulin levels were observed along with the restoration of glycogen content and the activities of carbohydrate metabolic enzymes in quercitrin-treated diabetic rats. The histopathological study of the pancreas revealed the protective role of quercitrin. There was an expansion of the islets and decreased fatty infiltrate of the islets in quercitrin treated diabetic rats. In normal rats treated with quercitrin, we could not observe any significant change in all the parameters studied. Combined, these results show that quercitrin plays a positive role in carbohydrate metabolism and antioxidant status in diabetic rats.
引用
收藏
页码:357 / 364
页数:8
相关论文
共 50 条
[41]   SELENIUM - BIOCHEMICAL ROLE AS A COMPONENT OF GLUTATHIONE PEROXIDASE [J].
ROTRUCK, JT ;
POPE, AL ;
GANTHER, HE ;
SWANSON, AB ;
HAFEMAN, DG ;
HOEKSTRA, WG .
SCIENCE, 1973, 179 (4073) :588-590
[42]   COLORIMETRIC ASSAY OF CATALASE [J].
SINHA, AK .
ANALYTICAL BIOCHEMISTRY, 1972, 47 (02) :389-&
[43]   PHARMACOLOGICAL STUDIES OF HOUTTUYNIAE-HERBA - THE ANTIINFLAMMATORY EFFECT OF QUERCITRIN [J].
TAGUCHI, K ;
HAGIWARA, Y ;
KAJIYAMA, K ;
SUZUKI, Y .
YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 1993, 113 (04) :327-333
[44]   Relation between antioxidant enzyme gene expression and antioxidative defense status of insulin-producing cells [J].
Tiedge, M ;
Lortz, S ;
Drinkgern, J ;
Lenzen, S .
DIABETES, 1997, 46 (11) :1733-1742
[45]   Antidiabetic effects of quercetin in streptozocin-induced diabetic rats [J].
Vessal, M ;
Hernmati, M ;
Vasei, M .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, 2003, 135 (03) :357-364
[46]   Quercitrin, a glycoside form of quercetin, prevents lipid peroxidation in vitro [J].
Wagner, Caroline ;
Fachinetto, Roselei ;
Dalla Corte, Cristiane Lenz ;
Brito, Veronica Bidinotto ;
Severo, Diego ;
Costa Dias, Gilvan de Oliveira ;
Morel, Ademir F. ;
Nogueira, Cristina W. ;
Rocha, Joao B. T. .
BRAIN RESEARCH, 2006, 1107 :192-198
[47]  
Wallert MA, 2001, BIOCHEM MOL BIOL EDU, V29, P199, DOI 10.1016/S1470-8175(01)00070-4
[48]   STREPTOZOTOCIN AND ALLOXAN INDUCE DNA STRAND BREAKS AND POLY(ADP-RIBOSE) SYNTHETASE IN PANCREATIC-ISLETS [J].
YAMAMOTO, H ;
UCHIGATA, Y ;
OKAMOTO, H .
NATURE, 1981, 294 (5838) :284-286
[49]   New approaches in the treatment of type 2 diabetes [J].
Zhang, BB ;
Moller, DE .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2000, 4 (04) :461-467
[50]   Hypoglycemic effect of Rehmannia glutinosa oligosaccharide in hyperglycemic and alloxan-induced diabetic rats and its mechanism [J].
Zhang, RX ;
Zhou, JH ;
Ha, ZP ;
Zhang, YX ;
Gu, GM .
JOURNAL OF ETHNOPHARMACOLOGY, 2004, 90 (01) :39-43