Quero Javier, Paesa Mónica, Morales Carmen, Mendoza Gracia, Osada Jesús, Teixeira José António, Ferreira-Santos Pedro, Rodríguez-Yoldi María Jesús
Department of Pharmacology and Physiology, Forensic and Legal Medicine, Veterinary Faculty, University of Zaragoza, 50013 Zaragoza, Spain.
Department of Chemical Engineering, University of Zaragoza, Campus Río Ebro-Edificio I+D, C/Poeta Mariano Esquillor S/N, 50018 Zaragoza, Spain.
Antioxidants (Basel). 2024 Jul 27;13(8):908. doi: 10.3390/antiox13080908.
(BE) is a mushroom well known for its taste, nutritional value, and medicinal properties. The objective of this work was to study the biological effects of BE extracts on human colon carcinoma cells (Caco-2), evaluating parameters related to oxidative stress and inflammation. In this study, a hydroethanolic extract of BE was obtained by ohmic heating green technology. The obtained BE extracts are mainly composed of sugars (mainly trehalose), phenolic compounds (taxifolin, rutin, and ellagic acid), and minerals (K, P, Mg, Na, Ca, Zn, Se, etc.). The results showed that BE extracts were able to reduce cancer cell proliferation by the induction of cell cycle arrest at the G0/G1 stage, as well as cell death by autophagy and apoptosis, the alteration of mitochondrial membrane potential, and caspase-3 activation. The extracts modified the redox balance of the cell by increasing the ROS levels associated with a decrease in the thioredoxin reductase activity. Similarly, BE extracts attenuated Caco-2 inflammation by reducing both and mRNA expression and COX-2 protein expression. In addition, BE extracts protected the intestine from the oxidative stress induced by HO. Therefore, this study provides information on the potential use of BE bioactive compounds as anticancer therapeutic agents and as functional ingredients to prevent oxidative stress in the intestinal barrier.
巴西蘑菇(BE)是一种以其味道、营养价值和药用特性而闻名的蘑菇。这项工作的目的是研究BE提取物对人结肠癌细胞(Caco-2)的生物学效应,评估与氧化应激和炎症相关的参数。在本研究中,通过欧姆加热绿色技术获得了BE的水乙醇提取物。所获得的BE提取物主要由糖类(主要是海藻糖)、酚类化合物(花旗松素、芦丁和鞣花酸)和矿物质(钾、磷、镁、钠、钙、锌、硒等)组成。结果表明,BE提取物能够通过诱导细胞周期停滞在G0/G1期来减少癌细胞增殖,以及通过自噬和凋亡导致细胞死亡、线粒体膜电位改变和半胱天冬酶-3激活。提取物通过增加与硫氧还蛋白还原酶活性降低相关的活性氧水平来改变细胞的氧化还原平衡。同样,BE提取物通过降低 和 的mRNA表达以及COX-2蛋白表达来减轻Caco-2炎症。此外,BE提取物保护肠道免受过氧化氢诱导的氧化应激。因此,本研究提供了关于BE生物活性化合物作为抗癌治疗剂以及作为预防肠道屏障氧化应激的功能成分的潜在用途的信息。