Moringa oleifera Lam. leaves are commonly used for diabetes worldwide. To date, there has been no research study done to investigate its effect on lipid and carbohydrate profile in Algerian diabetic patients. This pilot clinical study aimed to evaluate its long term-effect on lipid and carbohydrate profile in Algerian diabetic patients in preparation for a larger trial. 44 diabetic patients from Adrar city were administrated with 3600 mg of MO leaves powder twice a day at breakfast and at 7 p.m. for a period of 90 consecutive days, along with their regular hypoglycemic medications, in order to evaluate their serum lipid (TC, C-HDL, C-LDL and TG) and carbohydrate profile (blood sugar and HBA1c), weight, BMI and blood pressure, across five time-points (on days 0, 3, 7, 30, and 90). The results showed that oral administration of Moringa oleifera powder had a statistically significant effect on blood sugar (HBA1c), LDL-C, HDL-C levels in diabetic patients (p<0.05). Moringa oleifera leaf powder seemed reduced LDL-C, and HBA1c and elevated HDL-C, in diabetic patients. No side effect was reported by any participant. However, it did not have a statistically significant effect on weight, BMI and blood pressure. The data from the present clinical trial provide persuasive, although preliminary evidence supporting the therapeutic potential of Moringa oleifera leaf powder for managing chronic hyperglycemia and dyslipidemia in Algerian patients with diabetes. A more extensive trial is necessary to determine the Moringa oleifera leaf powder optimal dose and evaluate if its effect results into long-term advantages. In addition, further investigations are required to clear the underlying mechanisms involved with these effects.
The present work is carried out to evaluate biological activities of tubers extracts of Bunium mauritanicum. The methanol extract yield had higher (7.81%) tha n that of the aqueous extract (6.79%). The quantitative analysis of total phenols and flavonoid revealed that the highest concentration was recorded for the methanoic fraction with 89,442 ± 5,951μg EAG mg and 4.031 ± 0.141 μg EQ mg of extract respectively. In addition, the aqueous extract of tubers represents the most important antioxidant activity with an IC 50 of 0.14 mg ml against 2,2 diphenyl 1 picryl hydrazyl (DPPH Wherea s, the two extracts of the tubers have low reducing capacities compared to standard with EC 50 equal to 0.048 mg/ ml for the methanolic extract, 0.018 mg ml for t he aqueous extract and 0.009 mg/ ml for ascorbic acid. The methano l ic and aqueous extracts of Bunium mauritanicum reacted positively at least on one of the bacterial strains studied.
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