通过UPLC-MS/MS代谢物谱分析比较Plumbago zeylanica L.的不同部分并评估其抗氧化和抗真菌潜力

Lei Zeng , Yingle Chen , Liting Liang , Liu Yang , Song Wang , Qiaoguang Li , Zhihong Wang
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引用次数: 0

摘要

使用 70% 的乙醇从 Plumbago zeylanica L. (P.zeylanica)的叶(BHY)、根(BHG)和茎(BHJ)中提取代谢物。随后,对提取物的代谢物概况、抗真菌和抗氧化活性进行了评估。BHJ 中的总酚(91.63±1.08 mg GAE/g DW)和总黄酮(146.5±5.48 mg RE/g DW)含量最高。P.zeylanica 的所有提取物都能有效中和 DPPH(5 毫克/毫升时为 83.47 %-93.44 %)和 ABTS 自由基(5 毫克/毫升时为 99.42 %-102.1 %),显示出强大的抗氧化特性,尤其是在 BHG 中。与阳性对照抗坏血酸相比,P.zeylanica 提取物(3.0 毫克/毫升)的 DPPH 活性显示出更高的自由基清除活性。P.zeylanica 提取物对所有测试微生物(B.cinerea、F.moniliforme、B.dothidea、P.expansum 和 G.candidum)都有显著的抗真菌作用,抑制率在 37.96 % 到 99.65 % 之间,MIC 值在 0.063 到 1.00 mg/mL 之间。最易感的菌株是念珠菌(平均抑制率:95.47%)。BHG 在抑制 P.expansum、G.candidum 和 F.moniliforme 的生长方面效果最佳,而 BHJ 对 B.cinerea 和 B.dothidea 的活性最强。通过 UPLC-MS/MS 鉴定出 2116 种代谢物,其中 2026 种是三种提取物共有的。值得注意的是,BHG 是生物碱和醌类化合物(包括具有药理活性的化合物 plumbagin)的丰富来源,具有卓越的抗氧化和抗真菌能力。大部分代谢物都是首次在 P.zeylanica 中分离和鉴定到的,包括 Hydroxyplumbagic acid、3′-O-Beta-D-xylopyranosyl plumbagic acid、Loliolide、Atractylolide III、Cinchonain Ib 和 Cinchonain Ic。相关性分析确定了 115 个潜在的代谢生物标志物,主要包括酚酸、黄酮类化合物和生物碱,这可能是所观察到的生物活性强的部分原因。就上述结果而言,由于其显著的抗氧化和抗真菌特性,P.zeylanica 的所有部分都可以作为生物活性化合物的一种有前途的来源,在食品、化妆品和制药业中具有潜在的应用价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of different parts of Plumbago zeylanica L. through UPLC-MS/MS metabolite profiling and evaluation of their antioxidant and antifungal potential
The metabolites were extracted from the leaves (BHY), roots (BHG), and stems (BHJ) of Plumbago zeylanica L. (P.zeylanica) using 70 % ethanol. Subsequently, the metabolite profiles, antifungal, and antioxidant activities of the extracts were evaluated. The highest contents of total phenols (91.63±1.08 mg GAE/g DW) and total flavonoids (146.5±5.48 mg RE/g DW) were found in BHJ. All extracts of P.zeylanica effectively neutralized DPPH (83.47 %-93.44 % in 5 mg/mL) and ABTS radicals (99.42 %-102.1 % at 5 mg/mL), demonstrating potent antioxidant properties, particularly in BHG. The DPPH activity of P.zeylanica extracts (3.0 mg/mL) showed higher radical scavenging activity when compared with the positive control, ascorbic acid. The extracts of P.zeylanica displayed significant antifungal effects against all tested microorganisms (B.cinerea, F.moniliforme, B.dothidea, P.expansum, and G.candidum), with inhibition rates ranging from 37.96 % to 99.65 % and MIC values between 0.063 and 1.00 mg/mL. The most susceptible strain was G.candidum (average inhibition rate: 95.47 %). BHG demonstrated the highest effectiveness in inhibiting the growth of P.expansum, G.candidum, and F.moniliforme, while BHJ showed the strongest activity against B.cinerea and B.dothidea. 2116 metabolites were identified by UPLC-MS/MS, of which 2026 were common to the three extracts. Notably, BHG was found to be a rich source of alkaloids and quinones (including the pharmacologically active compound plumbagin), with superior antioxidant and antifungal capacities. Most of the metabolites were isolated and identified for the first time in P.zeylanica, including Hydroxyplumbagic acid, 3′-O-Beta-D-xylopyranosyl plumbagic acid, Loliolide, Atractylolide III, Cinchonain Ib, and Cinchonain Ic. Correlation analysis identified 115 potential metabolic biomarkers, primarily consisting of phenolic acids, flavonoids, and alkaloids, which likely explain some of the potent observed bioactivity. As regards the results mentioned above, all parts of the P.zeylanica could be utilized as a promising source of bioactive compounds for potential applications in the food, cosmetic, and pharmaceutical industries due to its notable antioxidant and antifungal properties.
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