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在健康促进应用中替代合成化合物的生物潜力:它是一个有前途的候选者吗?

The Biopotential of in Replacing Synthetic Compounds for Health-Promoting Applications: Is It a Promising Candidate?

作者信息

Cetiz Mehmet Veysi, Yagi Sakina, Sinan Kouadio Ibrahime, Senkardes Ismail, Koyuncu Ismail, Yuksekdag Ozgur, Caprioli Giovanni, Santanatoglia Agnese, Sagratini Gianni, Saka Enver, Ozturk Gulsah, Akgul Bengusu Hacer, Zengin Gokhan

机构信息

Department of Medical Biochemistry Faculty of Medicine, Harran University Turkey.

Department of Botany Faculty of Science, University of Khartoum Khartoum Sudan.

出版信息

Food Sci Nutr. 2025 Apr 14;13(4):e70109. doi: 10.1002/fsn3.70109. eCollection 2025 Apr.

Abstract

(L.) All. (family Orobanchaceae) is a facultative hemiparasitic plant used traditionally to cure many diseases. The present study was designed to evaluate the phenolic constituents, antioxidant, enzyme inhibitory, and cytotoxic properties of the aerial parts of . Ethyl acetate (EtOAc), ethanol (EtOH), and 70% EtOH extracts were prepared by maceration, while the aqueous extract was prepared by infusion. Rutin, 4-hydroxy benzoic acid, ferulic acid, -coumaric acid, hyperoside, delphinidin 3,5 diglucoside, kaempferol, and isoquercitrin were identified in most extracts with variable concentrations, but generally, the EtOH or 70% EtOH accumulated the highest contents. The 70% EtOH extract displayed the best antiradical (DPPH = 13.55 mg TE/g; ATBS = 53.78 mg TE/g) and ion-reducing (CUPRAC = 50.09 mg TE/g; FRAP = 24.73 mg TE/g) properties. The aqueous extract recorded the highest chelating iron power (12.91 mg EDTAE/g) while EtOAc and EtOH exerted the highest total antioxidant activity (2.29 and 2.49 mmol TE/g,  > 0.05). The best cholinesterase (anti-AChE = 2.91 mg GALAE/g; and anti-BchE = 2.62 mg GALAE/g) and α-glucosidase (1.19 mmol ACAE/g) inhibition activity was recorded from the EtOH extract, while that against the α-amylase was obtained from the EtOAc extract (0.69 mmol ACAE/g). The plant was most cytotoxic toward the HT-29 cell line, where the best effect was exerted by the 70% EtOH (IC 38.42 μg/mL) extract. Furthermore, network pharmacology analysis revealed critical gene targets and pathways associated with the bioactive compounds. Molecular docking studies revealed favorable binding modes and interaction patterns of major compounds with key colon cancer-related proteins, which were further supported by molecular dynamics simulations. As the first investigation into the phenolic composition and pharmacological effects of , this study highlights its potential as a promising source of bioactive compounds with therapeutic relevance for oxidative stress-related conditions.

摘要

独脚金属(列当属,列当科)是一种兼性半寄生植物,传统上用于治疗多种疾病。本研究旨在评估列当地上部分的酚类成分、抗氧化、酶抑制和细胞毒性特性。通过浸渍法制备乙酸乙酯(EtOAc)、乙醇(EtOH)和70%乙醇提取物,通过浸泡法制备水提取物。在大多数提取物中鉴定出了芦丁、4-羟基苯甲酸、阿魏酸、对香豆酸、金丝桃苷、飞燕草素3,5-二葡萄糖苷、山奈酚和异槲皮苷,其浓度各不相同,但总体而言,乙醇或70%乙醇提取物中的含量最高。70%乙醇提取物表现出最佳的抗自由基(DPPH = 13.55 mg TE/g;ATBS = 53.78 mg TE/g)和还原离子(CUPRAC = 50.09 mg TE/g;FRAP = 24.73 mg TE/g)特性。水提取物的螯合铁能力最高(12.91 mg EDTAE/g),而乙酸乙酯和乙醇提取物的总抗氧化活性最高(2.29和2.49 mmol TE/g,P>0.05)。乙醇提取物对胆碱酯酶的抑制活性最佳(抗AChE = 2.91 mg GALAE/g;抗BchE = 2.62 mg GALAE/g),对α-葡萄糖苷酶的抑制活性最佳(1.19 mmol ACAE/g),而对α-淀粉酶的抑制作用则来自乙酸乙酯提取物(0.69 mmol ACAE/g)。该植物对HT-29细胞系的细胞毒性最大,其中70%乙醇提取物(IC50 = 38.42 μg/mL)的效果最佳。此外,网络药理学分析揭示了与生物活性化合物相关的关键基因靶点和途径。分子对接研究揭示了主要化合物与关键结肠癌相关蛋白的良好结合模式和相互作用模式,分子动力学模拟进一步支持了这一点。作为对列当酚类成分和药理作用的首次研究,本研究突出了其作为生物活性化合物的潜在来源的价值,这些化合物对与氧化应激相关的疾病具有治疗意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce80/11997016/74616aba9c31/FSN3-13-e70109-g003.jpg

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