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  J. Med. Plants Res.

 

  Vol. 3 No. 9
 

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  articles by:
 

 Yibchok-anun S

 Adisakwattana S

 


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Journal of Medicinal Plants Research Vol. 3 (9), pp. 646–651, September 2009

ISSN 1996-0875 © 2009 Academic Journals  

   

 

Full Length Research Paper

 

 
 

Insulin secreting and a-glucosidase inhibitory activity of Coscinium fenestratum and postprandial hyperglycemia in normal and diabetic rats

 

Sirintorn Yibchok-anun1*, Wanlaya Jittaprasatsin1, Damrong Somtir2, Wijit Bunlunara3, Sirichai Adisakwattana4

 

1Department of Pharmacology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand.

2Department of Chemistry, Faculty of Science, Mahanakorn Technology University, Bangkok, Thailand.

3Department of Pathology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand.

4The Medical Food Research and Development Center, Department of Transfusion Medicine, Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok, Thailand.

 

*Corresponding author. E-mail: sirintorn.y@chula.ac.th.

 

Accepted 19 August, 2009

 
     
 

Abstract

 
     
 

This work focused on the effect of Coscinium fenestratum ethanolic extract on plasma glucose concentrations in normal and streptozotocin (STZ)-induced diabetic rats, the stimulatory effect on insulin secretion from perfused rat pancreas and the inhibitory effects on rat intestinal α-glucosidase enzymes, maltase and sucrase. In oral glucose, maltose and sucrose loading tests, the extract (250 - 1,000 mg/kg) significantly decreased plasma glucose concentrations in a dose-dependent manner. The extract (1,000 mg/kg) was most effective in decreasing plasma glucose concentrations and the response was closed to those of glibenclamide (5 mg/kg) and acarbose (3 mg/kg). In perfused rat pancreas, the extract (10 µg/ml) stimulated insulin secretion in a biphasic pattern. However, the berberine at the same dose as the extract slightly increased insulin secretion by 1.33-fold over the basal control group. In addition, the extract inhibited the activities of both maltase and sucrase with the IC50 of 3.89 and 11.22 mg/ml, respectively. Our findings suggest that the C. fenestratum ethanolic extract exerted anti-hyperglycemic activity by stimulating insulin secretion and a-glucosidase inhibition.

 

Key words: Coscinium fenestratum, streptozotocin, a-glucosidase, insulin secretion, perfused rat pancreas.

 

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