Antidiabetic activity of Boerhaavia diffusa L.: effect on hepatic key enzymes in experimental diabetes
Journal of Ethnopharmacology, ISSN: 0378-8741, Vol: 91, Issue: 1, Page: 109-113
2004
- 186Citations
- 99Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations186
- Citation Indexes186
- 186
- CrossRef79
- Captures99
- Readers99
- 99
Article Description
The purpose of this study was to investigate the effects of daily oral administration of aqueous solution of Boerhaavia diffusa L. leaf extract (BLEt) (200 mg/kg) for 4 weeks on blood glucose concentration and hepatic enzymes in normal and alloxan induced diabetic rats. A significant decrease in blood glucose and significant increase in plasma insulin levels were observed in normal and diabetic rats treated with BLEt. Treatment with BLEt resulted in a significant reduction of glycosylated haemoglobin and an increase in total haemoglobin level. The activities of the hepatic enzymes such as hexokinase was significantly increased and glucose-6-phosphatase, fructose-1,6-bisphosphatase were significantly decreased by the administration of BLEt in normal and diabetic rats. An oral glucose tolerance test (OGTT) was also performed in the same groups, in which there was a significant improvement in glucose tolerance in rats treated with BLEt. A comparison was made between the action of BLEt and antidiabetic drug—glibenclamide (600 μg/kg). The effect of BLEt was more prominent when compared to glibenclamide.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0378874103004549; http://dx.doi.org/10.1016/j.jep.2003.12.013; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=1442302300&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/15036478; https://linkinghub.elsevier.com/retrieve/pii/S0378874103004549; https://dx.doi.org/10.1016/j.jep.2003.12.013
Elsevier BV
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