5 research outputs found
In vivo antiplasmodial activity evaluation of the leaves of Ruta chalepensis L. (Rutaceae) against Plasmodium berghei
Ruta chalepensis has been used in the Eastern Africa for management of malaria despite lack of scientific evaluations. This study was carried out to evaluate the in vivo antiplasmodial activity of the 80% methanol extract of the leaves of the plant. The screening was done using Swiss albino mice against chloroquine sensitive rodent malaria parasite, Plasmodium berghei, following the standard 4-day suppressive test procedure. Three extract doses (100,200 and 400 mg/kg/day) were given orally. Parasitemia level, survival time as well as weight variation were measured for evaluating antiplasmodial efficacy. Moreover, preliminary phytochemical and acute toxicity studies were carried out.The presence of alkaloids, flavonoids, polyphenols, terpenoids, cardiac glycosides as well as saponins was confirmed. The oral LD50 was determined to be higher than 2000mg/kg. Antiplamodial activity of the extract was inversely related with the dose so that the100mg/kg dose was the most effective (mean parasitemia of 29.92 +0.94 on day 4,
Evaluation of Antidiabetic Activity of Ajuga integrifolia (Lamiaceae) Root Extract and Solvent Fractions in Mice
Traditional healers and the community have used the roots of Ajuga integrifolia for the treatment of diabetes mellitus. It is not scientifically validated for its antidiabetic activity previously. Therefore, the objective of the present study was to determine the hypoglycemic and antidiabetic activity of Ajuga integrifolia. Ajuga integrifolia roots’ crude extract and solvent fractions were prepared. The doses of 100 mg/kg, 200 mg/kg, and 400 mg/kg of crude root extract and solvent fractions were used on normoglycemic, oral glucose loaded, and streptozotocin-induced diabetic mice models to determine their hypoglycemic and antihyperglycemic activities. The crude extract and solvent fractions’ effect on bodyweight was also evaluated on streptozotocin-induced diabetic mice. A standard drug in all cases was glibenclamide (5 mg/kg), and the blood glucose level was measured by using a glucose meter. Data analysis was performed by using Statistical Package for Social Sciences version 21. One-way analysis of variance followed by Tukey’s post hoc multiple comparison test was used to analyze the data. p value < 0.05 was considered statistically significant. Hydromethanolic crude extract and its aqueous fraction of Ajuga integrifolia root showed a considerable blood glucose lowering activity at all doses. Both the repeated daily doses of the crude extract and the repeated daily doses of the aqueous fraction of Ajuga integrifolia root extract revealed the similar effect in lowering the fasting blood glucose level in streptozotocin-induced diabetic mice models. It was also found that groups treated with the Ajuga integrifolia at the doses of 200 mg/kg and 400 mg/kg showed significant (p<0.05) bodyweight improvement at the 14th day of treatment compared to the respective baseline bodyweight, and the diabetic control group showed significant (p<0.01) reduction in bodyweight at the 14th day compared to the baseline. This study revealed that crude extract and solvent fractions of Ajuga integrifolia root possess significant antidiabetic activity which supports its traditional use for the treatment of diabetes mellitus