柽柳水提液和甲醇提液抗氧化和抗糖尿病活性的研究。

Q4 Pharmacology, Toxicology and Pharmaceutics
K. Loucif, Fatima Benchikh, Chawki Ben Souici, Smain Amira
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引用次数: 0

摘要

氧化应激在糖尿病并发症的发展中起着重要作用;因此,使用天然抗氧化剂作为糖尿病的治疗剂是可能的。本研究旨在通过证实其抗氧化剂、α-淀粉酶和α-葡萄糖苷酶的抑制潜力,从刺山鹅膏中寻找酚类物质的重要来源,并证实该植物可能是医学上重要的天然化合物的重要来源。采用2,2′-二苯基-1-丙酰肼(DPPH)自由基清除、金属螯合和铜还原抗氧化能力等方法对其抗氧化性能进行了研究。采用体外模型研究了α-淀粉酶和α-葡萄糖苷酶的抑制活性。此外,还测定了试验提取物中多酚和黄酮类化合物的含量。与水提取物相比,甲醇提取物表现出最高的酚类和类黄酮含量。然而,水提取物具有最强的抗氧化活性(DPPH清除、金属螯合和铜离子还原抗氧化能力)、α-淀粉酶和α-葡萄糖苷酶抑制作用。酚类物质的含量与木犀提取物的抗氧化和酶抑制活性之间没有相关性。结果表明,这种植物可能是医学上重要的天然化合物的重要来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antioxidant and antidiabetic activities of aqueous and methanolic extracts from Athamanta sicula L.
Oxidative stress plays a major role in the development of diabetes complications; therefore, it is possible to use natural antioxidants as therapeutic agents for diabetes. This study aimed to find an important source of phenolics from Athamanta sicula L. (A. sicula) and confirm that this plant could be a significant source of medically important natural compounds, by confirming its antioxidant, α-amylase and α-glucosidase inhibitory potential. Antioxidant property was performed using 2,2′-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging, metal chelating, and cupric reducing antioxidant capacity methods. The α-amylase and α-glucosidase inhibitory activities were investigated using an in vitro model. Moreover, polyphenols and flavonoids contents of the tested extracts were carried out. The methanolic extract exhibited the highest phenolic and flavonoids content compared to aqueous extract. However, aqueous extract possessed the strongest antioxidant activity (DPPH scavenging, metal chelating, and Cupric ion reducing antioxidant capacities), α-amylase and α-glucosidase inhibitory effects. No correlation between phenolics content and antioxidant and enzyme inhibitory activities of A. sicula L. extracts was observed. The results showed that this plant could be a significant source of medically important natural compounds.
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来源期刊
Current Enzyme Inhibition
Current Enzyme Inhibition Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
1.30
自引率
0.00%
发文量
30
期刊介绍: Current Enzyme Inhibition aims to publish all the latest and outstanding developments in enzyme inhibition studies with regards to the mechanisms of inhibitory processes of enzymes, recognition of active sites, and the discovery of agonists and antagonists, leading to the design and development of new drugs of significant therapeutic value. Each issue contains a series of timely, in-depth reviews written by leaders in the field, covering a range of enzymes that can be exploited for drug development. Current Enzyme Inhibition is an essential journal for every pharmaceutical and medicinal chemist who wishes to have up-to-date knowledge about each and every development in the study of enzyme inhibition.
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