Balci Neslihan, Aslan Kubra, Erturk Adem, Gulcin Ilhami
Dursun Keles Health Services Vocational School Gumushane University Gumushane Türkiye.
Faculty of Science, Chemistry Department Ataturk University Erzurum Türkiye.
Food Sci Nutr. 2025 Jul 21;13(7):e70654. doi: 10.1002/fsn3.70654. eCollection 2025 Jul.
This study evaluates the antioxidant activity, enzyme inhibition potential, and phenolic composition of ethanolic Siran propolis extract. Antioxidant capacity was measured using reducing power (CUPRAC, FRAP, and Fe-reducing) and radical scavenging (DPPH·, ABTS·, and DMPD·) assays. The extract showed strong reducing ability, surpassing standard antioxidants in CUPRAC and FRAP assays, correlating with high ferulic acid (40.40 mg/g) and p-coumaric acid (88.60 mg/g) levels identified by LC-MS/MS. While it demonstrated notable DPPH· scavenging (IC: 30.14 μg/mL), ABTS activity was weaker (IC: 272.44 μg/mL). Enzyme inhibition assays indicated effective inhibition of α-glycosidase, AChE (IC: 2.15 μg/mL), hCA I, and hCA II. Notably, AChE inhibition was stronger than the standard tacrine inhibitor (IC: 8.82 μg/mL), suggesting neuroprotective potential. The observed bioactivities are attributed to synergistic effects of phenolic acids and flavonoids, including quercetin, luteolin, taxifolin, and resveratrol. These findings highlight Siran propolis as a promising natural antioxidant and enzyme inhibitor source with potential therapeutic applications and food formulations.
本研究评估了乙醇提取的西兰蜂胶提取物的抗氧化活性、酶抑制潜力和酚类成分。使用还原能力(CUPRAC、FRAP和铁还原)和自由基清除(DPPH·、ABTS·和DMPD·)试验来测量抗氧化能力。该提取物显示出很强的还原能力,在CUPRAC和FRAP试验中超过了标准抗氧化剂,这与通过LC-MS/MS鉴定出的高阿魏酸(40.40 mg/g)和对香豆酸(88.60 mg/g)水平相关。虽然它表现出显著的DPPH·清除能力(IC:30.14 μg/mL),但ABTS活性较弱(IC:272.44 μg/mL)。酶抑制试验表明该提取物能有效抑制α-糖苷酶、乙酰胆碱酯酶(IC:2.15 μg/mL)、人碳酸酐酶I和人碳酸酐酶II。值得注意的是,乙酰胆碱酯酶抑制作用比标准他克林抑制剂更强(IC:8.82 μg/mL),表明具有神经保护潜力。观察到的生物活性归因于酚酸和黄酮类化合物的协同作用,包括槲皮素、木犀草素、花旗松素和白藜芦醇。这些发现突出了西兰蜂胶作为一种有前景的天然抗氧化剂和酶抑制剂来源,具有潜在的治疗应用和食品配方应用价值。