首页> 美国卫生研究院文献>Toxins >Cytotoxicity Genotoxicity and Disturbance of Cell Cycle in HepG2 Cells Exposed to OTA and BEA: Single and Combined Actions
【2h】

Cytotoxicity Genotoxicity and Disturbance of Cell Cycle in HepG2 Cells Exposed to OTA and BEA: Single and Combined Actions

机译:暴露于OTA和BEA的HepG2细胞的细胞毒性遗传毒性和细胞周期紊乱:单一和联合作用。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Mycotoxins are produced by a number of fungal genera spp., for example, Aspergillus, Penicillium, Alternaria, Fusarium, and Claviceps. Beauvericin (BEA) and Ochratoxin A (OTA) are present in various cereal crops and processed grains. This goal of this study was to determine their combination effect in HepG2 cells, presented for the first time. In this study, the type of interaction among BEA and OTA through an isobologram method, cell cycle disturbance by flow cytometry, and genotoxic potential by in vitro micronucleus (MN) assay following the TG 487 (OECD, 2016) of BEA and OTA individually and combined in HepG2 cells are presented. Cytotoxic concentration ranges studied by the MTT assay over 24, 48, and 72 h were from 0 to 25 µM for BEA and from 0 to 100 µM for OTA, while BEA + OTA combinations were at a 1:10 ratio from 3.4 to 27.5 µM. The toxicity observed for BEA was higher than for OTA at all times assayed; additive and synergistic effects were detected for their mixtures. Cell cycle arrest in the G0/G1 phase was detected for OTA and BEA + OTA treatments in HepG2 cells. Genotoxicity revealed significant effects for BEA, OTA, and in combinations underlining the importance of studying real exposure scenarios of chronic exposure to mycotoxins.
机译:霉菌毒素是由许多真菌属产生的,例如曲霉菌,青霉菌,链格孢菌,镰刀菌和锁虫。白曲霉素(BEA)和O曲毒素A(OTA)存在于各种谷物作物和加工谷物中。这项研究的目的是确定它们在首次出现的HepG2细胞中的联合作用。在这项研究中,分别通过BEA和OTA的TG 487(OECD,2016)和等位线图方法,通过等效线图法确定BEA和OTA之间的相互作用类型,流式细胞术对细胞周期的干扰以及体外微核(MN)测定的遗传毒性潜力。介绍了在HepG2细胞中的结合。在24、48和72小时内,MTT分析研究的细胞毒性浓度范围对于BEA为0至25 µM,对于OTA为0至100 µM,而BEA + OTA组合的比例为1:10,为3.4至27.5 µM 。在所有测试时间中,BEA的毒性均高于OTA。检测了它们混合物的加和协同作用。对于HepG2细胞中的OTA和BEA + OTA处理,检测到G0 / G1期细胞周期停滞。遗传毒性揭示了对BEA,OTA的显着影响,并综合显示了研究长期暴露于霉菌毒素的真实暴露场景的重要性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号