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利用色谱法、光谱法和网络药理学方法,建立土耳其植物区系中Mill.的化学成分与生物活性之间的联系。

Establishing a link between the chemical composition and biological activities of Mill. from the Turkish flora utilizing , and network pharmacological methodologies.

作者信息

Zengin Gokhan, Cetiz Mehmet Veysi, Abul Nurgul, Gulcin Ilhami, Caprioli Giovanni, Piatti Diletta, Ricciutelli Massimo, Koyuncu Ismail, Yuksekdag Ozgur, Bahşi Muammer, Güler Osman, Aumeeruddy Muhammad Zakariyyah, Mahomoodally Mohamad Fawzi

机构信息

Department of Biology, Faculty of Science, Selcuk University, Konya, Turkey.

Department of Bioinformatics, Biozentrum der Universität Würzburg, Würzburg, Germany.

出版信息

Toxicol Mech Methods. 2025 Feb;35(2):146-166. doi: 10.1080/15376516.2024.2397387. Epub 2024 Sep 8.

Abstract

OBJECTIVES

Five solvent extracts (n-hexane, ethyl acetate, ethanol, ethanol/water (70%), and water) of Mill. from Turkey were evaluated for chemical and biological properties.

METHODS

Antioxidant activities, inhibitory properties against key enzymes involved in the etiology of chronic diseases were tested, as well as cytotoxic effects on different cell lines. Chemical characterization was also carried out to determine the most abundant compounds of each extract.

RESULTS

The highest total phenolic content (TPC) was observed in the water extract while highest TFC in ethanol/water extract. The most abundant compounds in the extracts were hyperoside (69041.06 mg kg), isoquercitrin (46239.49 mg kg), delphindin-3,5-diglucoside (42043.81 mg kg), myricetin (21486.61 mg kg), and kaempferol-3-glucoside (21199.76 mg kg). Molecular dynamic (MD) simulations confirmed the structural stability and dynamic conformational integrity of these complexes over a period of 100 ns. In network pharmacology, A total of 657 unique target genes were screened: 52 associated with programmed cell death-1 (PD-1), 85 with vascular endothelial growth factor receptor-2 (VEGFR2), and 130 with fibroblast growth factor receptor-2 (FGFR2), identifying crucial gene interactions for these proteins. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were conducted, revealing significant interactions and pathways such as the advanced glycation end products (AGE) and their receptors (RAGE) signaling pathway in diabetic complications and T- helper 17 (Th17) cell differentiation, among others. This elucidation of complex networks involving key genes like AKT Serine/Threonine Kinase 1 (AKT1), MYC proto-oncogene (MYC), tumor protein 53 (TP53), Interleukin 6 (IL6), and tumor necrosis factor (TNF) provides a promising foundation for the development of targeted therapies in the treatment of non-communicable diseases.

CONCLUSION

These results show that could be a natural source of potent antioxidants and enzyme inhibitors which need to be further explored for the development of biopharmaceuticals.

摘要

目的

对采自土耳其的千屈菜的五种溶剂提取物(正己烷、乙酸乙酯、乙醇、乙醇/水(70%)和水)的化学和生物学特性进行评估。

方法

测试了抗氧化活性、对慢性病病因中关键酶的抑制特性以及对不同细胞系的细胞毒性作用。还进行了化学表征以确定每种提取物中含量最丰富的化合物。

结果

水提取物中总酚含量(TPC)最高,而乙醇/水提取物中总黄酮含量(TFC)最高。提取物中含量最丰富的化合物为金丝桃苷(69041.06毫克/千克)、异槲皮苷(46239.49毫克/千克)、飞燕草素-3,5-二葡萄糖苷(42043.81毫克/千克)、杨梅素(21486.61毫克/千克)和山奈酚-3-葡萄糖苷(21199.76毫克/千克)。分子动力学(MD)模拟证实了这些复合物在100纳秒的时间段内的结构稳定性和动态构象完整性。在网络药理学中,共筛选出657个独特的靶基因:52个与程序性细胞死亡蛋白1(PD-1)相关,85个与血管内皮生长因子受体2(VEGFR2)相关,130个与成纤维细胞生长因子受体2(FGFR2)相关,确定了这些蛋白质的关键基因相互作用。进行了基因本体论(GO)和京都基因与基因组百科全书(KEGG)通路富集分析,揭示了诸如糖尿病并发症中的晚期糖基化终产物(AGE)及其受体(RAGE)信号通路和辅助性T细胞17(Th17)细胞分化等显著的相互作用和通路。对涉及关键基因如丝氨酸/苏氨酸蛋白激酶1(AKT1)、原癌基因MYC(MYC)、肿瘤蛋白53(TP53)、白细胞介素6(IL6)和肿瘤坏死因子(TNF)的复杂网络的阐明为开发治疗非传染性疾病的靶向疗法提供了有前景的基础。

结论

这些结果表明千屈菜可能是强效抗氧化剂和酶抑制剂的天然来源,在生物制药开发方面需要进一步探索。

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