In silico, in vitro and ex-vivo Toxicological Profiling of 5,7,4'-Trihydroxyflavone-8 -C-ß-Glucopyranoside - Vitexin

A. Sousa, Maria Denise Leite Ferreira, D. Fernandes, L. Cordeiro, M. F. Souza, H. Pessôa, A. A. O. Filho, R. C. S. Sá
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Abstract

This study aimed to evaluate the in silico, in vitro, and ex-vivo toxicity of vitexin, the flavonoid 5,7,4'- trihydroxyflavone-8-C-β-glucopyranoside from Waltheria viscosissima. The chemical structure and predicted bioactive properties were also in silico analyzed. The in vitro and ex-vivo assays were performed according to the Ethics Code of the World Medical Association and were approved by the Ethics Committee of University Center of Patos (protocol number: 3.621.284). In silico analysis suggested that the molecule presents good oral bioavailability and good absorption; penetrating biological membranes. The toxicity tests revealed the potential effectiveness of the molecule in cellular protection against free radicals, in addition to possible antimutagenic, anticarcinogenic, antioxidant, antineoplastic, anti-inflammatory, anti-hemorrhagic and apoptosis agonist activity. Hemolytic and genotoxic assessment detected low hemolysis rates in human red blood cells and no cellular toxicity against oral mucosa cells. The data suggest that vitexin is a safe molecule for possible therapeutic application and its toxicity profile indicates viability for future studies.
5,7,4'-三羟黄酮-8 - c -ß-葡萄糖苷-牡荆苷体外和离体毒性分析
本研究旨在评价牡荆素类黄酮5,7,4′-三羟基黄酮-8- c -β-葡萄糖吡喃苷的体内、体外和体外毒性。并对其化学结构和预测的生物活性进行了计算机分析。体外和离体试验按照世界医学协会伦理准则进行,并经帕托斯大学中心伦理委员会批准(协议号:3.621.284)。硅分析表明该分子具有良好的口服生物利用度和良好的吸收;穿透生物膜。毒性试验揭示了该分子对自由基的潜在保护作用,以及可能的抗诱变、抗癌、抗氧化、抗肿瘤、抗炎、抗出血和细胞凋亡激动剂活性。溶血和遗传毒性评估发现,人红细胞溶血率低,对口腔粘膜细胞无细胞毒性。这些数据表明牡荆素是一种安全的分子,可能用于治疗,其毒性谱显示了未来研究的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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