Diabetes mellitus is a major health problem that threatens the whole world. According to
WHO reports, the prevalence of diabetic patients in egyptis expected to increase from 2,623,000
in 2000 to be 6,726,000 in 2030. Metformin is the first line drug for type 2 diabetes mellitus,
which can be used alone or in combination with other drugs. However, the concomitant use of
metformin with stevia needs more investigation to clarify the role of this combination as a new
strategy in type 2 diabetes mellitus.
Type 2 diabetes mellitus was induced in rats by i.p. injection of STZ and NA. Animals were
divided into five groups, each contains 8 rats. Group I: negative control, group II: diabetic
control received saline, group III: diabetic rats received 400 mg/kg/day stevia aqueous extract,
group IV: diabetic rats received metformin 250 mg/kg/day, group V: diabetic rats received
stevia 400 mg/kg/day + metformin 250 mg/kg/day. After 3 weeks blood samples were collected,
animals were sacrificed and tissue samples were collected. Biochemical parameters including
FBG, serum insulin, serum DPP-4, TC, TG, LDL, HDL, GSH and MDA were measured by
colorimetric and ELISA methods.
Both stevia and metformin significantly reduced FBG level. While serum insulin
significantly increased. Serum DPP-4 was significantly reduced in all treated groups,
concerning lipid profile, stevia and metformin significantly lowered TC, TG, LDLand increased
HDL. Both stevia and metformin significantly decreased MDA and increased GSH compared to
diabetic rats. In addition, stevia significantly improved the antidiabetic effects of metformin.
Stevia has an antihyperglycemic effect and could increase the antidiabetic activity of
metformin. DPP-4 attenuation, antioxidant and insulin-sensitizing effects may be involved in the
antidiabetic action of stevia. Regarding lipid profile stevia showed hypolipidemic effect.
Research Journal
Bulletin of Pharmaceutical Sciences. Assiut
Research Publisher
Assiut University, Faculty of Pharmacy
Research Rank
2
Research Vol
vol.42
Research Website
https://journals.ekb.eg/article_62264.html
Research Year
2019
Research Member
Research Abstract