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Research Article
2 (
1
); 133-146

The protective effect of Moringa olifera against complications of type2 diabetes mellitus in male albino rats.

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This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
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This article was originally published by Qassim University and was migrated to Scientific Scholar after the change of Publisher.

Abstract

Background: Diabetes mellitus, particularly type 2 (T2DM), is one of the most common diseases. T2DM has been associated with stress and a change in lifestyle. Regulation of postprandial blood glucose levels and the use of some natural plant extracts with inhibitory actions against carbohydrate digestion enzymes like alpha-amylase and fewer adverse effects than synthetic medicines are potential methods for preventing dietary carbohydrate absorption. This study shows the anti-diabetic effects of Moringa olifera extract on insulin and blood glucose in diabetic rats given streptozotocin (STZ) treatment. Methods: The experiment was performed on 40 Wistar male rats; the experimental study included 4 groups: (I) normal rats and (II)normal rats orally received an aqueous extract of Moringa (500 mg/kg/day) for consecutive 4 weeks (III)diabetic group; male albino rats injected with a single intraperitoneal dose of Streptozotocin 55 mg/kg b.w.t. (IV) Streptozotocin-treated rats received an aqueous extract of Moringa 500 mg/kg/day orally for consecutive 4weeks. Results: The results of the following study showed that the injection of STZ resulted in a decline in insulin and an increase in glucose. It was also revealed that Moringa olifera extract has more anti-diabetic effect against streptozotocin treatment due to its higher phenolic content and its effect on decreasing the activity of α-amylase. This suggests that MAE leaf decreased postprandial glucose levels by slowing amylase-mediated glucose uptake.


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