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Antidiabetic Potential of Root Extract of Momordica cymbalaria, Fenzl in Streptozotocin Induced Diabetic Rats


Affiliations
1 Shri Sarvajanik Pharmacy College, Nr. Arvind Baug, Mehsana-384 001, Gujarat, India
2 Visveswarapura Institute of Pharmaceutical Sciences, NA, 24th Main, 25th Cross, BSK Stage II, Bangalore - 560 004 Karnataka, India
     

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The effect of a aqueous extract of the ischolar_mains of Momordica cymbalaria Fenzl., (Cucurbitaceae) was evaluated with streptozotocin(65 mg/kg, i.p.) induced diabetic rats. Seventy-two hours after streptozotocin injection, the extract, at doses of 250 and 500 mg/kg, was administered orally for 30 consecutive days. Oral glucose tolerance test (OGTT) and In-vitro peripheral glucose uptake studies were also measured during this course of experiment. The extract was found to be potent antidiabetic as evidenced by significant (p < 0.001) reduction of serum glucose level of diabetic rats on 30th day by both the doses (maximal effect of 45.95% reduction of serum glucose level, at 500 mg/kg, p < 0.001). Results demonstrated a significant reduction of serum lipids (maximal effect of 50.23 and 31.89% reduction of cholesterol and triglyceride, respectively, at 500 mg/kg, p < 0.001) and elevation of liver glycogen level (maximal effect at 300 mg/kg, p < 0.05) in diabetic rats, comparable to that of standard antidiabetic glibenclamide at 500 μg/kg, p.o. In OGTT, the extract at different doses showed significant reduction in serum glucose level (p < 0.05) from 30 min. onwards. The extract also revealed increase in In-vitro model for peripheral glucose uptake (not statistically significant). Improvement of body weight profile was also observed in extract-treated diabetic rats.

Keywords

Momordica cymbalaria, Streptozotocin Induced Diabetes, Antihyperglycemic, Antidiabetic Effect.
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  • Antidiabetic Potential of Root Extract of Momordica cymbalaria, Fenzl in Streptozotocin Induced Diabetic Rats

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Authors

K. M. Modh
Shri Sarvajanik Pharmacy College, Nr. Arvind Baug, Mehsana-384 001, Gujarat, India
I. S. Anand
Shri Sarvajanik Pharmacy College, Nr. Arvind Baug, Mehsana-384 001, Gujarat, India
B. Panigrahi
Shri Sarvajanik Pharmacy College, Nr. Arvind Baug, Mehsana-384 001, Gujarat, India
C. N. Patel
Shri Sarvajanik Pharmacy College, Nr. Arvind Baug, Mehsana-384 001, Gujarat, India
R. Badmanaban
Shri Sarvajanik Pharmacy College, Nr. Arvind Baug, Mehsana-384 001, Gujarat, India
M. V. Patel
Visveswarapura Institute of Pharmaceutical Sciences, NA, 24<sup>th</sup> Main, 25<sup>th</sup> Cross, BSK Stage II, Bangalore - 560 004 Karnataka, India

Abstract


The effect of a aqueous extract of the ischolar_mains of Momordica cymbalaria Fenzl., (Cucurbitaceae) was evaluated with streptozotocin(65 mg/kg, i.p.) induced diabetic rats. Seventy-two hours after streptozotocin injection, the extract, at doses of 250 and 500 mg/kg, was administered orally for 30 consecutive days. Oral glucose tolerance test (OGTT) and In-vitro peripheral glucose uptake studies were also measured during this course of experiment. The extract was found to be potent antidiabetic as evidenced by significant (p < 0.001) reduction of serum glucose level of diabetic rats on 30th day by both the doses (maximal effect of 45.95% reduction of serum glucose level, at 500 mg/kg, p < 0.001). Results demonstrated a significant reduction of serum lipids (maximal effect of 50.23 and 31.89% reduction of cholesterol and triglyceride, respectively, at 500 mg/kg, p < 0.001) and elevation of liver glycogen level (maximal effect at 300 mg/kg, p < 0.05) in diabetic rats, comparable to that of standard antidiabetic glibenclamide at 500 μg/kg, p.o. In OGTT, the extract at different doses showed significant reduction in serum glucose level (p < 0.05) from 30 min. onwards. The extract also revealed increase in In-vitro model for peripheral glucose uptake (not statistically significant). Improvement of body weight profile was also observed in extract-treated diabetic rats.

Keywords


Momordica cymbalaria, Streptozotocin Induced Diabetes, Antihyperglycemic, Antidiabetic Effect.

References