Shirokov Alexander, Grinev Vyacheslav, Kanevskiy Matvey, Fedonenko Yulia, Matora Larisa, Polukonova Natalya, Mudrak Dmitry, Mylnikov Artyom, Polukonova Anna, Bucharskaya Alla, Navolokin Nikita, Maslyakova Galina
Simbioz Center for the Collective Use of Research Equipment, Institute of Biochemistry and Physiology of Plants and Microorganisms, Saratov Scientific Centre of the Russian Academy of Sciences (IBPPM RAS), Saratov, Russia.
Department of Biochemistry and Biophysics, N.G. Chernyshevsky Saratov National Research State University, Saratov, Russia.
Anticancer Agents Med Chem. 2025;25(6):388-398. doi: 10.2174/0118715206323280241029215900.
L. (hedge hyssop), a medicinal plant of the Scrophulariaceae family, has diuretic, purgative, and vermifuge properties. It is used as a herbal tea to treat chronic gastroenteritis, renal colic, jaundice, and intestinal worms. Previously, we have found that an extract from is nontoxic and has antitumor, antioxidant, antimicrobial, antiinflammatory, anticachexic, and other properties. Our aims in this study were to separate the extract into individual fractions, to identify the most biologically active fractions, and to examine the chemical composition of these fractions and their biological activity toward A498 renal carcinoma cells.
The extract was fractionated by reversed-phase high-performance liquid chromatography, and each fraction was tested for antitumor activity. The active fractions were characterized by UV-visible electron spectral analysis, circular dichroism analysis, Fourier transform infrared spectroscopy, high-performance liquid chromatography, electrospray ionization tandem mass spectrometry, and nuclear magnetic resonance spectroscopy.
Two antitumor-active fractions of a flavonoid nature were isolated and chromatographically purified. On the basis of the nuclear magnetic resonance data, the aglycone fragment of the main component of one fraction was found to be structured as 2-(3,4-dimethoxyphenyl)-7-hydroxychroman-4-one, or 3',4'-dimethoxy-7- hydroxyflavanone.
The antitumor effect of the most active fraction containing 7-O-glucoside of apigenin, glycoside 7,3'-di-O-luteolin and trace amounts of eupatilin against renal carcinoma A498 cells was manifested in its cytotoxic, cytostatic, apoptotic and autophagosomal activities. In addition, we found 3-(1-2)-glucoside of soyaspogenol B, which is a pentacyclic triterpenoid in the structure.
L.(水八角)是玄参科的一种药用植物,具有利尿、通便和驱虫特性。它被用作草药茶来治疗慢性肠胃炎、肾绞痛、黄疸和肠道寄生虫。此前,我们发现L.的提取物无毒,具有抗肿瘤、抗氧化、抗菌、抗炎、抗恶病质等特性。本研究的目的是将L.提取物分离成各个组分,鉴定出生物活性最强的组分,并研究这些组分的化学成分及其对A498肾癌细胞的生物活性。
通过反相高效液相色谱法对提取物进行分离,对每个组分进行抗肿瘤活性测试。通过紫外可见电子光谱分析、圆二色性分析、傅里叶变换红外光谱、高效液相色谱、电喷雾电离串联质谱和核磁共振光谱对活性组分进行表征。
分离并色谱纯化了两个具有黄酮类性质的抗肿瘤活性组分。根据核磁共振数据,发现其中一个组分的主要成分的苷元片段结构为2-(3,4-二甲氧基苯基)-7-羟基色满-4-酮,即3',4'-二甲氧基-7-羟基黄酮。
含有芹菜素7-O-葡萄糖苷、7,3'-二-O-木犀草素苷和痕量灯盏乙素的最活性组分对肾癌细胞A498的抗肿瘤作用表现为细胞毒性、细胞生长抑制、凋亡和自噬体活性。此外,我们发现了大豆皂醇B的3-(1-2)-葡萄糖苷,其结构为五环三萜。