Enzyme Inhibitory Properties, Antioxidant Activities, and Phytochemical Profile of Three Medicinal Plants from Turkey

Q1 Pharmacology, Toxicology and Pharmaceutics Advances in Pharmacological Sciences Pub Date : 2015-12-20 DOI:10.1155/2015/410675
G. Zengin, G. Guler, A. Aktumsek, R. Ceylan, C. M. N. Picot, M. Mahomoodally
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引用次数: 39

Abstract

We aimed to investigate the inhibitory potential of three medicinal plants (Hedysarum varium, Onobrychis hypargyrea, and Vicia truncatula) from Turkey against key enzymes involved in human pathologies, namely, diabetes (α-amylase and α-glucosidase), neurodegenerative disorders (tyrosinase, acetylcholinesterase, and butyrylcholinesterase), and hyperpigmentation (tyrosinase). The antioxidant potential, phenolic and flavonoid content of ethyl acetate, and methanolic and aqueous extracts were investigated using in vitro assays. The total antioxidant capacity (TAC), β-carotene/linoleic acid bleaching activity, 1,1-diphenyl-2-picrylhydrazyl free radical (DPPH•), 2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS•+), cupric ion reducing antioxidant capacity (CUPRAC), ferric reducing antioxidant power (FRAP), and metal chelating activity on ferrous ions were used to evaluate the antioxidant capabilities of the extracts. The half-maximal inhibitory concentrations (IC50) of the extracts on cholinesterase, tyrosinase, and α-amylase were significantly higher than the references, galantamine, kojic acid, and acarbose, respectively. The half-maximal effective concentrations (EC50) of the extracts on TAC, CUPRAC, and FRAP were significantly higher than trolox. The phenol and flavonoid contents of the plant extracts were in the range 20.90 ± 0.190–83.25 ± 0.914 mg gallic acid equivalent/g extract and 1.45 ± 0.200–39.71 ± 0.092 mg rutin equivalent/g extract, respectively. The plants were found to possess moderate antioxidant capacities and interesting inhibitory action against key enzymes.
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土耳其三种药用植物的酶抑制特性、抗氧化活性和植物化学特征
本研究旨在研究土耳其三种药用植物(Hedysarum varum, Onobrychis hypargyrea和Vicia truncatula)对糖尿病(α-淀粉酶和α-葡萄糖苷酶)、神经退行性疾病(酪氨酸酶、乙酰胆碱酯酶和丁基胆碱酯酶)和色素沉着(酪氨酸酶)等与人类病理相关的关键酶的抑制潜力。采用体外测定法研究了乙酸乙酯、甲醇和水提物的抗氧化能力、酚类和类黄酮含量。以总抗氧化能力(TAC)、β-胡萝卜素/亚油酸漂白活性、1,1-二苯基-2-吡啶酰肼自由基(DPPH•)、2,2-氮基-双(3-乙基苯并噻唑-6-磺酸)(ABTS•+)、铜离子还原抗氧化能力(CUPRAC)、铁离子还原抗氧化能力(FRAP)和对铁离子的金属螯合活性等指标评价提取物的抗氧化能力。提取物对胆碱酯酶、酪氨酸酶和α-淀粉酶的半最大抑制浓度(IC50)均显著高于对照物加兰他明、曲酸和阿卡波糖。提取物对TAC、CUPRAC和FRAP的半最大有效浓度(EC50)显著高于trolox。提取物中苯酚含量为20.90±0.190 ~ 83.25±0.914 mg没食子酸当量/g,类黄酮含量为1.45±0.200 ~ 39.71±0.092 mg芦丁当量/g。这些植物具有中等的抗氧化能力和对关键酶的抑制作用。
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来源期刊
Advances in Pharmacological Sciences
Advances in Pharmacological Sciences PHARMACOLOGY & PHARMACY-
CiteScore
6.40
自引率
0.00%
发文量
0
审稿时长
14 weeks
期刊介绍: Advances in Pharmacological and Pharmaceutical Sciences is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies in all areas of experimental and clinical pharmacology, pharmaceutics, medicinal chemistry and drug delivery. Topics covered by the journal include, but are not limited to: -Biochemical pharmacology, drug mechanism of action, pharmacodynamics, pharmacogenetics, pharmacokinetics, and toxicology. -The design and preparation of new drugs, and their safety and efficacy in humans, including descriptions of drug dosage forms. -All areas of medicinal chemistry, such as drug discovery, design and synthesis. -Basic biology of drug and gene delivery through to application and development of these principles, through therapeutic delivery and targeting. Areas covered include bioavailability, controlled release, microcapsules, novel drug delivery systems, personalized drug delivery, and techniques for passing biological barriers.
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