|Number of pages||12|
|Publication status||Published - 2006|
Antidiabetic activity of benzyl tetra isoquinoline alkaloid berberine in streptozotocin-nicotinamide induced type 2 diabetic rats. / Punitha, I.S.R.; Shirwaikar, A.In: Diabetologia Croatica, Vol. 34, No. 4, 2006, p. 117-128.
Research output: Contribution to journal › Article
TY - JOUR
T1 - Antidiabetic activity of benzyl tetra isoquinoline alkaloid berberine in streptozotocin-nicotinamide induced type 2 diabetic rats
AU - Punitha, I.S.R.
AU - Shirwaikar, A.
N1 - Cited By :32 Export Date: 10 November 2017 CODEN: DBCRB Correspondence Address: Shirwaikar, A.; Department of Pharmacognosy, Manipal College of Pharmaceutical Sciences, Manipal, Karnataka 576 104, India; email: email@example.com Chemicals/CAS: glycosylated hemoglobin, 9062-63-9; streptozocin, 18883-66-4 References: Stermitz, F.R., Lorenz, P., Tawara, J.N., Zenewica, L.A., Lewis, K., Synergy in a medicinal plant: Antimicrobial action of berberine potentiated by 5′-methoxyhydrocarpin a multidrug pump inhibitor (2001) Proc Natl Acad Sci USA, 97, pp. 1433-1437; Amin, A.H., Subbaiah, T.V., Abbasi, K.M., Berberine sulfate: Antimicrobial activity, bioassay and mode of action (1969) Can J Microbiol, 15, pp. 1067-1076; Mahajan, V.M., Sharma, A., Rattan, A., Antimycotic activity of berberine sulphate: An alkaloid from an Indian medicinal herb (1982) Sabouraudia, 20, pp. 79-81; Subbaiah, T.V., Amin, A.H., Effect of berberine sulfate on Entamoeba histolytica (1967) Nature, 215, pp. 527-528; Gudima, S.O., Memelova, L.V., Borodulin, V.B., Kinetic analysis of interaction of human immunodeficiency virus reverse transcriptase with alkaloids (1994) Mol Biol (Mosk), 28, pp. 1308-1314; 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PY - 2006
Y1 - 2006
N2 - The antidiabetic potential of berberine was evaluated in a streptozotocin-nicotinamide induced type 2 diabetic rat model. On administration of graded doses of berberine to normal and experimental diabetic rats for 12 days, a significant (p <0.05) reduction was, observed in fasting blood glucose levels. However, serum insulin levels failed to be stimulated on treatment with berberine. Significant changes were observed in serum lipid profiles, thiobarbituric acid reactive substance levels, glycosylated hemoglobin and liver glycogen levels in berberine treated diabetic rats as compared with diabetic control and normal animals. The effect of berberine was also studied for its carbohydrate metabolism and antioxidant status in streptozotocin- nicotinamide induced type 2 diabetic rats. Oral administration of berberine caused a significant increase in both enzymatic and nonenzymatic antioxidants. Studies of the effect of berberine on glycolytic enzymes showed a significant increase in their levels whilst a significant decrease was observed in the levels of the gluconeogenic enzymes in treated diabetic rats. Serum creatinine and urea levels also declined significantly.
AB - The antidiabetic potential of berberine was evaluated in a streptozotocin-nicotinamide induced type 2 diabetic rat model. On administration of graded doses of berberine to normal and experimental diabetic rats for 12 days, a significant (p <0.05) reduction was, observed in fasting blood glucose levels. However, serum insulin levels failed to be stimulated on treatment with berberine. Significant changes were observed in serum lipid profiles, thiobarbituric acid reactive substance levels, glycosylated hemoglobin and liver glycogen levels in berberine treated diabetic rats as compared with diabetic control and normal animals. The effect of berberine was also studied for its carbohydrate metabolism and antioxidant status in streptozotocin- nicotinamide induced type 2 diabetic rats. Oral administration of berberine caused a significant increase in both enzymatic and nonenzymatic antioxidants. Studies of the effect of berberine on glycolytic enzymes showed a significant increase in their levels whilst a significant decrease was observed in the levels of the gluconeogenic enzymes in treated diabetic rats. Serum creatinine and urea levels also declined significantly.
M3 - Article
VL - 34
SP - 117
EP - 128
JO - Diabetologia Croatica
JF - Diabetologia Croatica
SN - 0351-0042
IS - 4