Gluconeogenesis inhibition and phytochemical composition of two Cecropia species

被引:52
作者
Andrade-Cetto, Adolfo [1 ]
Cardenas Vazquez, Rene [2 ]
机构
[1] Univ Nacl Autonoma Mexico, Fac Ciencias, Lab Etnofarmacol, Mexico City 04511, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Fac Ciencias, Lab Biol Anim Expt, Mexico City 04511, DF, Mexico
关键词
Cecropia obtusifolia; Cecropia peltata; Hypoglycemic agent; Type; 2; diabetes; Medicinal plant; Gluconeogenesis; CHLOROGENIC ACID; OBTUSIFOLIA BERTOL; EXTRACTS; GLUCOSE;
D O I
10.1016/j.jep.2010.04.016
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Aim of the study: Cecropia obtusifolia and Cecropia peltata are plants highly used by the Mexican diabetic population to treat type 2 diabetes. Previous studies have assessed their hypoglycemic effect in animal models and in type 2 diabetic patients. Both plants contain cholorogenic acid, an inhibitor of glucose-6-phosphate translocase. In this work, we found a mechanism by which to understand how these plants could produce the observed hypoglycemic effect according to their traditional use. To test the hypothesis that targeting gluconeogenesis with an inhibitor of Gl-6-P translocase could result in a reduction of hepatic glucose production, we examined the effects of Cecropia obtusifolia and Cecropia peltata on gluconeogenesis (in vivo) and the activity of the enzyme (in vitro). Materials and methods: The extracts of the two plants were analyzed by HPLC to confirm their phytochemical composition. To test the inhibition of gluconeogenesis in vivo, a pyruvate tolerance test (2 g/kg) was performed in 18-h fasted n5-STZ rats. The effect of the extracts (Cecropia obtusifolia and Cecropia peltata 150 mg/kg) on glucose-6-phosphatase activity was assayed in vitro with intact rat liver microsomes. Results: Using HPLC-DAD, we confirmed that the main components of both species are chlorogenic acid and isoorientin. Diabetic rats treated with the extracts showed a lower glucose curve. The tested extracts were able to reduce the increase in the glucose blood level, and they inhibited the glucose-6-P activity with IC(50)s of 224 mu g/ml for Cecropia obtusifolia aqueous, 160 mu g/ml for Cecropia obtusifolia butanolic, 146 mu g/ml for Cecropia peltata aqueous and 150 mu g/ml for Cecropia peltata butanolic. Conclusions: The results of the experiments presented here suggest that the administration of both plants can improve glycemic control by blocking the hepatic glucose output, especially in the fasting state. These data support the traditional use of the plants as "agua de uso", a cold infusion of the plant consumed over the course of a day. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:93 / 97
页数:5
相关论文
共 21 条
[1]
Mexican plants with hypoglycaemic effect used in the treatment of diabetes [J].
Andrade-Cetto, A ;
Heinrich, M .
JOURNAL OF ETHNOPHARMACOLOGY, 2005, 99 (03) :325-348
[2]
Hypoglycemic effect of Cecropia obtusifolia on streptozotocin diabetic rats [J].
Andrade-Cetto, A ;
Wiedenfeld, H .
JOURNAL OF ETHNOPHARMACOLOGY, 2001, 78 (2-3) :145-149
[3]
Andrade-Cetto A., 2007, PHARMACOLOGYONLINE, V3, P203
[4]
ANDRADECETTO A, 1999, THESIS NATL U MEXICO, P97
[5]
ANDRADECETTO A, 1995, THESIS UNAM MEXICO, P93
[6]
ARION WJ, 1989, METHOD ENZYMOL, V174, P58
[7]
Chlorogenic acid and hydroxynitrobenzaldehyde: New inhibitors of hepatic glucose 6-phosphatase [J].
Arion, WJ ;
Canfield, WK ;
Ramos, FC ;
Schindler, PW ;
Burger, HJ ;
Hemmerle, H ;
Schubert, G ;
Below, P ;
Herling, AW .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 339 (02) :315-322
[8]
DeFronzo R., 2009, PATHOGENESIS TYPE 2
[9]
Contributions by kidney and liver to glucose production in the postabsorptive state and after 60 h of fasting [J].
Ekberg, K ;
Landau, BR ;
Wajngot, A ;
Chandramouli, V ;
Efendic, S ;
Brunengraber, H ;
Wahren, J .
DIABETES, 1999, 48 (02) :292-298
[10]
Chlorogenic acid and synthetic chlorogenic acid derivatives: Novel inhibitors of hepatic glucose-6-phosphate translocase [J].
Hemmerle, H ;
Burger, HJ ;
Below, P ;
Schubert, G ;
Rippel, R ;
Schindler, PW ;
Paulus, E ;
Herling, AW .
JOURNAL OF MEDICINAL CHEMISTRY, 1997, 40 (02) :137-145