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使用液相色谱-电喷雾电离-四极杆飞行时间质谱对提取物进行综合代谢组学分析及生物活性研究

Comprehensive Metabolomic Profiling and Biological Activity Analysis of Extracts Using LC-ESI-QTOF-MS.

作者信息

Kalyniukova Alina, Ahmed Shakeel, Ak Gunes, Saka Enver, Duran Tugce, Abul Nurgul, Gulcin Ilhami, Senkardes Ismail, Cetiz Mehmet Veysi, Zengin Gokhan

机构信息

Faculty of Forestry and Wood Sciences Czech University of Life Sciences Prague Suchdol Czech Republic.

Physiology and Biochemistry Laboratory, Department of Biology, Science Faculty Selcuk University Konya Turkey.

出版信息

Food Sci Nutr. 2025 Sep 2;13(9):e70885. doi: 10.1002/fsn3.70885. eCollection 2025 Sep.

Abstract

The current investigation was designed to explore the chemical composition, antioxidant capacity, enzyme inhibitory activity, and cytotoxic potential of four different extracts (Ethyl Acetate, Ethanol, Ethanol/Water (70%) and Water) derived from the aerial parts of . In vitro, assessments were performed utilizing diverse antioxidant assays, along with evaluations of neuroprotective enzyme inhibition targeting acetylcholine and butyl choline enzymes, as well as antidiabetic activities against α-amylase and α-glucosidase and a potential candidate for a tyrosinase inhibitor. LC-ESI-QTOF-MS identification provided a total of 70 compounds in the extracted samples of , including kaempferol 3-(deoxyhexosyl-hexoside)-7-hexoside, rutin, quercetin dideoxyhexoside, caffeic acid hexoside, quinoline alkaloids, morphine derivatives, and scoulerine. Moreover, the ethanol extract exhibited the highest anti-AChE (2.39 mg GALAE/g), while ethyl acetate exhibited anti-BChE (3.31 mg GALAE/g), Ethanol/Water (70%) anti-tyrosinase (53.09 mg KAE/g) and anti-glucosidase (1.09 mmol ACAE/g) activities. Additionally, the ethyl acetate extract effectively inhibited carbonic anhydrase I and II isoenzymes. Furthermore, the ethanol and ethanol/water extracts demonstrated significant cytotoxicity against A549 lung cancer cells. However, partially/weakly triggers the apoptosis of cancer cells. Furthermore, the investigation identified 885 target genes for 's phytochemicals, 31 of which were familiar to insomnia. In silico studies demonstrated that protopine, rutin, eschscholtzidine, boldine, and (S)-scoulerine exhibited notable inhibitory effects on insomnia-related DRD5, DRD4, and SERT proteins. These findings highlight the potential pharmacological applications of the aerial parts of as a source for developing novel phytopharmaceuticals targeting various oxidative stress-related conditions, including diabetes, cancer, Alzheimer's disease, and insomnia.

摘要

当前的研究旨在探索从[植物名称]地上部分提取的四种不同提取物(乙酸乙酯、乙醇、乙醇/水(70%)和水)的化学成分、抗氧化能力、酶抑制活性和细胞毒性潜力。在体外,利用多种抗氧化测定方法进行评估,同时评估针对乙酰胆碱和丁酰胆碱酶的神经保护酶抑制作用,以及对α-淀粉酶和α-葡萄糖苷酶的抗糖尿病活性和作为酪氨酸酶抑制剂的潜在候选物。LC-ESI-QTOF-MS鉴定在[植物名称]的提取物样本中总共发现了70种化合物,包括山奈酚3-(脱氧己糖基-己糖苷)-7-己糖苷、芦丁、槲皮素二脱氧己糖苷、咖啡酸己糖苷、喹啉生物碱、吗啡衍生物和紫堇灵。此外,乙醇提取物表现出最高的抗乙酰胆碱酯酶活性(2.39毫克GALAE/克),而乙酸乙酯表现出抗丁酰胆碱酯酶活性(3.31毫克GALAE/克),乙醇/水(70%)表现出抗酪氨酸酶活性(53.09毫克KAE/克)和抗葡萄糖苷酶活性(1.09毫摩尔ACAE/克)。此外,乙酸乙酯提取物有效抑制碳酸酐酶I和II同工酶。此外,乙醇和乙醇/水提取物对A549肺癌细胞表现出显著的细胞毒性。然而,[植物名称]部分/微弱地触发癌细胞的凋亡。此外,该研究确定了[植物名称]植物化学物质的885个靶基因,其中31个与失眠有关。计算机模拟研究表明,原阿片碱、芦丁、埃氏紫堇定、波尔定和(S)-紫堇灵对与失眠相关的DRD5、DRD4和SERT蛋白表现出显著的抑制作用。这些发现突出了[植物名称]地上部分作为开发针对各种氧化应激相关病症(包括糖尿病、癌症、阿尔茨海默病和失眠)的新型植物药物来源的潜在药理学应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dec/12405063/2a76b682e418/FSN3-13-e70885-g003.jpg

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