Department of Applied Biology, University Larbi Tébessi Tebessa, 12000 Tebessa, Algeria.
Department of Biomedical Sciences, University of Sassari, Viale San Pietro 43/B, 07100 Sassari, Italy.
Molecules. 2019 Feb 10;24(3):612. doi: 10.3390/molecules24030612.
Grape leaves influence several biological activities in the cardiovascular system, acting as antioxidants. In this study, we aimed at evaluating the effect of ethanolic and water extracts from grape leaves grown in Algeria, obtained by accelerator solvent extraction (ASE), on cell proliferation. The amount of total phenols was determined using the modified Folin-Ciocalteu method, antioxidant activities were evaluated by the 2,2-diphenyl-l-picrylhydrazyl free radical (DPPH*) method and OH radical scavenging using electron paramagnetic resonance (EPR) spectroscopy methods. Cell proliferation of HepG2 hepatocarcinoma, MCF-7 human breast cancer cells and vein human umbilical (HUVEC) cells, as control for normal cell growth, was assessed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide reduction assay (MTT). Apoptosis- related genes were determined by measuring Bax and Bcl-2 mRNA expression levels. Accelerator solvent extractor yield did not show significant difference between the two solvents (ethanol and water) ( > 0.05). Total phenolic content of water and ethanolic extracts was 55.41 ± 0.11 and 155.73 ± 1.20 mg of gallic acid equivalents/g of dry weight, respectively. Ethanolic extracts showed larger amounts of total phenols as compared to water extracts and interesting antioxidant activity. HepG2 and MCF-7 cell proliferation decreased with increasing concentration of extracts (0.5, 1, and 2 mg/mL) added to the culture during a period of 1⁻72 h. In addition, the expression of the pro-apoptotic gene Bax was increased and that of the anti-apoptotic gene Bcl-2 was decreased in a dose-dependent manner, when both MCF-7 and HepG2 cells were cultured with one of the two extracts for 72 h. None of the extracts elicited toxic effects on vein umbilical HUVEC cells, highlighting the high specificity of the antiproliferative effect, targeting only cancer cells. Finally, our results suggested that ASE crude extract from grape leaves represents a source of bioactive compounds such as phenols, with potential antioxidants activity, disclosing a novel antiproliferative effect affecting only HepG2 and MCF-7 tumor cells.
葡萄叶在心血管系统中具有多种生物活性,可作为抗氧化剂。在这项研究中,我们旨在评估由加速溶剂萃取(ASE)获得的来自阿尔及利亚种植的葡萄叶的水提物和醇提物对细胞增殖的影响。使用改良的 Folin-Ciocalteu 法测定总酚含量,通过 2,2-二苯基-1-苦基肼自由基(DPPH*)法和电子顺磁共振(EPR)光谱法测定抗氧化活性。通过 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴化物还原测定法(MTT)评估 HepG2 肝癌、MCF-7 人乳腺癌细胞和静脉人脐静脉内皮(HUVEC)细胞的细胞增殖,作为正常细胞生长的对照。通过测量 Bax 和 Bcl-2 mRNA 表达水平来确定与细胞凋亡相关的基因。加速溶剂萃取器的产率在两种溶剂(乙醇和水)之间没有显著差异(>0.05)。水提物和醇提物的总酚含量分别为 55.41±0.11 和 155.73±1.20 mg 没食子酸当量/g 干重。与水提物相比,醇提物含有更多的总酚类物质,且具有有趣的抗氧化活性。随着提取物(0.5、1 和 2 mg/mL)添加到培养物中的浓度增加,HepG2 和 MCF-7 细胞的增殖在 1⁻72 h 期间降低。此外,当 MCF-7 和 HepG2 细胞在 72 h 内与两种提取物之一培养时,促凋亡基因 Bax 的表达增加,抗凋亡基因 Bcl-2 的表达减少。两种提取物对静脉脐静脉 HUVEC 细胞均无毒性作用,这突出表明了抗增殖作用的高度特异性,仅针对癌细胞。最后,我们的结果表明,葡萄叶的 ASE 粗提取物代表了酚类等生物活性化合物的来源,具有潜在的抗氧化活性,揭示了一种新的仅影响 HepG2 和 MCF-7 肿瘤细胞的增殖抑制作用。