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五种传统使用的本土抗糖尿病药用植物对α-淀粉酶、α-葡萄糖苷酶、葡萄糖截留及体外淀粉水解动力学的抑制潜力

Inhibitory Potential of Five Traditionally Used Native Antidiabetic Medicinal Plants on α -Amylase, α -Glucosidase, Glucose Entrapment, and Amylolysis Kinetics In Vitro.

作者信息

Picot Carene M N, Subratty A Hussein, Mahomoodally M Fawzi

机构信息

Department of Health Sciences, Faculty of Science, University of Mauritius, 230 Réduit, Mauritius.

出版信息

Adv Pharmacol Sci. 2014;2014:739834. doi: 10.1155/2014/739834. Epub 2014 Mar 2.

Abstract

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 α -amylase and α -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  μ g/mL, resp.) were found to significantly (P < 0.05) inhibit α -amylase and were comparable to acarbose. EL, EO, AM, and SL extracts (5000  μ g/mL) were found to significantly (P < 0.05) inhibit α -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 α -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.

摘要

对毛里求斯传统使用的五种抗糖尿病本土药用植物进行了研究,即线叶银胶菊(SL)、弯枝福氏木(FF)、月桂叶古柯(EL)、东方榄仁树(EO)和马达加斯加五月茶(AM),以探究其体外α -淀粉酶和α -葡萄糖苷酶抑制特性、葡萄糖截留能力及淀粉分解动力学。仅EL、EO和AM的甲醇提取物(分别为7472.92±5.99、1745.58±31.66和2222.96±13.69μg/mL)被发现能显著(P<0.05)抑制α -淀粉酶,且与阿卡波糖相当。EL、EO、AM和SL提取物(5000μg/mL)被发现能显著(P<0.05)抑制α -葡萄糖苷酶(抑制率在87.41±3.31%至96.87±1.37%之间)。酶动力学研究显示为非竞争性和混合型抑制。提取物表现出显著(P<0.05)的葡萄糖截留能力(葡萄糖扩散阻滞指数(GDRI)为8%至29%),其中SL活性更高(GDRI为29%)且呈浓度依赖性活性(分别为29%、26%、21%、14%和5%)。淀粉分解动力学研究表明,与水提取物相比,甲醇提取物是更强的α -淀粉酶抑制剂,且具有葡萄糖截留特性。我们的研究结果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型植物药开辟了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d2d/3958646/9e6400b58cb0/APS2014-739834.001.jpg

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