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稠李树树皮甲醇提取物的酶抑制活性、酚类成分分析及计算机模拟研究。

Enzyme Inhibitory Activities, Phenolic Profile, and In Silico Studies of Sorbus torminalis Tree Bark Methanol Extract.

机构信息

Department of Pharmacognosy, University of Belgrade - Faculty of Pharmacy, Vojvode Stepe 450, 11221, Belgrade, Serbia.

Department of Pharmacognosy, University of Banja Luka - Faculty of Medicine, Save Mrkalja 14, 78000, Banja Luka, Republic of Srpska.

出版信息

Chem Biodivers. 2024 Nov;21(11):e202401459. doi: 10.1002/cbdv.202401459. Epub 2024 Sep 25.

Abstract

The different parts of Sorbus torminalis (L.) Crantz are used in traditional medicine for various conditions such as cardiac diseases, cough, and diabetes, indicating its significant medicinal potential. Therefore, the current investigation aimed to reveal the phenolic composition of the poorly studied S. torminalis methanol extract of the bark, as well as its capacity to inhibit enzymes relevant to cardiovascular, neurodegenerative, and metabolic diseases. A total of 28 phenolic components, including 20 procyanidins aglycones (A- and B-type), four procyanidin glycosides, catechin and its glycoside, and two (epi)catechin derivatives, were detected using LC-MS. The contents of total polyphenols (6.22 %), total tannins (3.04 %), condensed tannins (0.70 %), and total flavonoids (0.24 %) were determined spectrophotometrically, highlighting the considerable phenolic richness of the examined plant material. The concentration-dependent ability to inhibit α-amylase (IC=130 μg /mL), α-glucosidase (IC=312.13 μg /mL), acetylcholinesterase (IC=156.46 μg /mL), butyrylcholinesterase (IC=217.68 μg /mL), and angiotensin-converting enzyme (IC=36.77 μg /mL) was demonstrated in vitro. The in silico approach showed that catechin, procyanidin B2 and C1, S. torminalis bark constituents, can form stable complexes with the target enzymes but with different binding affinity. The results supported the medicinal potential of S. torminalis bark and significantly expanded our knowledge of its chemistry, justifying further research.

摘要

稠李(Sorbus torminalis)的不同部位在传统医学中被用于治疗各种病症,如心脏病、咳嗽和糖尿病,这表明其具有重要的药用潜力。因此,目前的研究旨在揭示研究较少的稠李树皮甲醇提取物的酚类成分及其抑制与心血管、神经退行性和代谢性疾病相关的酶的能力。使用 LC-MS 检测到了 28 种酚类成分,包括 20 种原花青素苷元(A 型和 B 型)、4 种原花青素糖苷、儿茶素及其糖苷、两种(表)儿茶素衍生物。采用分光光度法测定总多酚(6.22%)、总单宁(3.04%)、缩合单宁(0.70%)和总类黄酮(0.24%)的含量,突出了所检查植物材料的相当丰富的酚类物质。体外实验证明,稠李树皮提取物具有浓度依赖性的抑制α-淀粉酶(IC=130μg/mL)、α-葡萄糖苷酶(IC=312.13μg/mL)、乙酰胆碱酯酶(IC=156.46μg/mL)、丁酰胆碱酯酶(IC=217.68μg/mL)和血管紧张素转化酶(IC=36.77μg/mL)的能力。基于计算机的方法表明,稠李树皮的组成成分儿茶素、原花青素 B2 和 C1 可以与靶酶形成稳定的复合物,但结合亲和力不同。这些结果支持了稠李树皮的药用潜力,并显著扩展了我们对其化学性质的认识,证明了进一步研究的合理性。

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