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风铃草(Campanula lyrata subsp. lyrata)提取物的靶向酚类分析、抗氧化活性及酶抑制潜力与分子对接见解

Targeted Phenolic Profiling, Antioxidant Activities, and Enzyme Inhibition Potential of Campanula lyrata subsp. lyrata Extracts With Molecular Docking Insights.

作者信息

Kargin Solmaz Fatma Ozlem, Kirkan Bulent, Istifli Erman Salih, Sarikurkcu Cengiz, Tepe Bektas

机构信息

Faculty of Pharmacy, Afyonkarahisar Health Sciences University, Afyonkarahisar, Türkiye.

Department of Biology, Faculty of Science and Literature, Cukurova University, Adana, Türkiye.

出版信息

J Food Sci. 2025 Aug;90(8):e70368. doi: 10.1111/1750-3841.70368.

DOI:10.1111/1750-3841.70368
PMID:40765313
Abstract

The growing interest in plant-based bioactives has intensified research into their therapeutic potential. This study investigated the chemical profile, antioxidant properties, and enzyme inhibitory effects of methanol extracts from Campanula lyrata subsp. lyrata, obtained via maceration (MAC-ME), Soxhlet (SOE-ME), and ultrasound-assisted extraction (UAE-ME). Among the extracts, MAC-ME contained the highest total phenolic (41.76 mg GAE/g) and flavonoid (23.68 mg RE/g) contents. In antioxidant assays, SOE-ME exhibited the strongest DPPH radical scavenging activity (IC: 1.17 mg/mL), while all extracts displayed comparable reducing power in CUPRAC and FRAP assays (EC: 0.50-0.77 mg/mL), indicating moderate antioxidant potential. Enzyme inhibition results revealed that SOE-ME showed the most potent AChE (IC: 1.18 ± 0.03 mg/mL) and tyrosinase (IC: 1.45 ± 0.01 mg/mL) inhibition, whereas MAC-ME demonstrated the highest α-amylase inhibition (IC: 2.11 ± 0.01 mg/mL). These findings suggest selective bioactivity profiles depending on the extraction technique. Molecular docking supported the in vitro results, showing strong binding affinities of chlorogenic acid (ΔG = -9.25 kcal/mol for AChE) and hesperidin (ΔG = -9.05 kcal/mol for α-amylase), with simultaneous docking indicating potential synergistic interactions (ΔG up to -12.65 kcal/mol). Overall, the extracts-especially SOE-ME-demonstrated promising multi-target bioactivity, underscoring the pharmacological potential of C. lyrata subsp. lyrata in managing oxidative stress and enzyme-related disorders.

摘要

对植物源生物活性成分日益增长的兴趣加剧了对其治疗潜力的研究。本研究调查了通过浸渍法(MAC-ME)、索氏提取法(SOE-ME)和超声辅助提取法(UAE-ME)获得的风铃草亚种风铃草甲醇提取物的化学概况、抗氧化特性和酶抑制作用。在提取物中,MAC-ME的总酚含量最高(41.76 mg GAE/g),黄酮含量最高(23.68 mg RE/g)。在抗氧化试验中,SOE-ME表现出最强的DPPH自由基清除活性(IC:1.17 mg/mL),而所有提取物在CUPRAC和FRAP试验中表现出相当的还原能力(EC:0.50 - 0.77 mg/mL),表明具有中等抗氧化潜力。酶抑制结果显示,SOE-ME对乙酰胆碱酯酶(IC:1.18 ± 0.03 mg/mL)和酪氨酸酶(IC:1.45 ± 0.01 mg/mL)的抑制作用最强,而MAC-ME对α-淀粉酶的抑制作用最高(IC:2.11 ± 0.01 mg/mL)。这些发现表明,根据提取技术的不同,生物活性谱具有选择性。分子对接支持了体外实验结果,显示绿原酸(对乙酰胆碱酯酶的ΔG = -9.25 kcal/mol)和橙皮苷(对α-淀粉酶的ΔG = -9.05 kcal/mol)具有很强的结合亲和力,同时对接表明存在潜在的协同相互作用(ΔG高达-12.65 kcal/mol)。总体而言,这些提取物——尤其是SOE-ME——表现出有前景的多靶点生物活性,突出了风铃草亚种风铃草在管理氧化应激和酶相关疾病方面的药理潜力。

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