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首页> 外文期刊>Advances in pharmacological sciences >Inhibitory Potential of Five Traditionally Used Native Antidiabetic Medicinal Plants on alpha-Amylase, alpha-Glucosidase, Glucose Entrapment, and Amylolysis Kinetics In Vitro
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Inhibitory Potential of Five Traditionally Used Native Antidiabetic Medicinal Plants on alpha-Amylase, alpha-Glucosidase, Glucose Entrapment, and Amylolysis Kinetics In Vitro

机译:五种传统使用的天然抗糖尿病药用植物对α-淀粉酶,α-葡萄糖苷酶,葡萄糖截留和淀粉分解动力学的抑制潜能

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Five traditionally used antidiabetic native medicinal plants of Mauritius, namely, Stillingia lineata (SL), Faujasiopsis flexuosa (FF), Erythroxylum laurifolium (EL), Elaeodendron orientale (EO), and Antidesma madagascariensis (AM), were studied for possible alpha-amylase and a-glucosidase inhibitory property, glucose entrapment, and amylolysis kinetics in vitro. Only methanolic extracts of EL, EO, and AM (7472.92 ± 5.99,1745.58 ±31.66, and 2222.96 ± 13.69 mug/mL, resp.) were found to significantly (P < 0.05) inhibit alpha-amylase and were comparable to acarbose. EL, EO, AM, and SL extracts (5000 mug/mL) were found to significantly (P < 0.05) inhibit a-glucosidase (between 87.41 ± 3.31 and 96.87 ± 1.37% inhibition). Enzyme kinetic studies showed an uncompetitive and mixed type of inhibition. Extracts showed significant (P < 0.05) glucose entrapment capacities (8 to 29% glucose diffusion retardation index (GDRI)), with SL being more active (29% GDRI) and showing concentration-dependent activity (29, 26, 21, 14, and 5%, resp.). Amylolysis kinetic studies showed that methanolic extracts were more potent inhibitors of a-amylase compared to aqueous extracts and possessed glucose entrapment properties. Our findings tend to provide justification for the hypoglycaemic action of these medicinal plants which has opened novel avenues for the development of new phytopharmaceuticals geared towards diabetes management.
机译:研究了毛里求斯的五种传统使用的抗糖尿病天然药用植物,分别为Stillingia lineata(SL),Faujasiopsis flexuosa(FF),Erythroxylum laurifolium(EL),Elaeodendron Orientale(EO)和Antidesma madagascariensis(AM),以寻找可能的α-淀粉酶。和α-葡萄糖苷酶的抑制特性,葡萄糖截留和体外淀粉分解动力学。发现仅EL,EO和AM的甲醇提取物(7472.92±5.99,1745.58±31.66和2222.96±13.69杯/毫升,分别)显着(P <0.05)抑制α-淀粉酶并且与阿卡波糖相当。发现EL,EO,AM和SL提取物(5000杯/毫升)显着(P <0.05)抑制α-葡萄糖苷酶(抑制率介于87.41±3.31和96.87±1.37%之间)。酶动力学研究显示了非竞争性和混合型抑制作用。提取物表现出显着的(P <0.05)葡萄糖截留能力(8至29%葡萄糖扩散阻滞指数(GDRI)),而SL的活性更高(29%GDRI),并且表现出浓度依赖性的活性(29,26,21,14,和5%)。淀粉分解动力学研究表明,与含水提取物相比,甲醇提取物是α-淀粉酶的更有效抑制剂,并且具有葡萄糖截留特性。我们的发现倾向于为这些药用植物的降血糖作用提供依据,这为开发针对糖尿病管理的新植物药开辟了新途径。

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