1. Vitis vinifera L. grape skin extract activates the insulin-signalling cascade and reduces hyperglycaemia in alloxan-induced diabetic mice.
- Author
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Soares de Moura R, da Costa GF, Moreira AS, Queiroz EF, Moreira DD, Garcia-Souza EP, Resende AC, Moura AS, and Teixeira MT
- Subjects
- Alloxan, Animals, Blood Glucose metabolism, Blotting, Western, Body Weight, Diabetes Mellitus, Experimental blood, Disease Models, Animal, Hyperglycemia blood, Male, Mice, Muscle, Skeletal metabolism, Receptor, Insulin metabolism, Diabetes Mellitus, Experimental drug therapy, Hyperglycemia drug therapy, Hypoglycemic Agents pharmacology, Insulin blood, Plant Extracts pharmacology, Vitis chemistry
- Abstract
Objectives: This study examined the effect of Vitis vinifera grape skin extract (ACH09) on hyperglycaemia and the insulin-signalling cascade in alloxan-treated mice., Methods: Glycaemia, serum insulin and Western blot analysis of insulin cascade proteins were evaluated in the gastrocnemius muscles of four groups of adult mice: control, ACH09 (200 mg/kg per day, p.o.), alloxan (300 mg/kg, i.p.) and alloxan + ACH09. Insulin secretion in isolated pancreatic islets was also studied., Key Findings: Glycaemia values in the alloxan + ACH09 and ACH09 groups were significantly lower than in the alloxan-treated and control groups, respectively. Increased insulin resistance (HOMA index) was observed in the alloxan-treated group but not in the alloxan + ACH09 group. Insulin receptor content and Akt phosphorylation were significantly greater in the alloxan + ACH09 group compared with the alloxan-treated group. The glucose transporter (GLUT-4) content was reduced in alloxan-treated mice compared with the control group, while alloxan + ACH09 and ACH09-treated mice showed a significant increase in GLUT-4 content. ACH09 treatment did not change glucose-induced insulin secretion in isolated pancreatic islets., Conclusions: The results suggest that ACH09 has hypoglycaemic and antihyperglycaemic effects that are independent of an increase in insulin release but are probably dependent on an increase in insulin sensitivity resulting from an activation of the insulin-signalling cascade in skeletal muscle., (© 2011 The Authors. JPP © 2011 Royal Pharmaceutical Society.)
- Published
- 2012
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