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首页> 外文期刊>Archives of Toxicology >Cytotoxic effects of BADGE (bisphenol A diglycidyl ether) and BFDGE (bisphenol F diglycidyl ether) on Caco-2 cells in vitro.
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Cytotoxic effects of BADGE (bisphenol A diglycidyl ether) and BFDGE (bisphenol F diglycidyl ether) on Caco-2 cells in vitro.

机译:BADGE(双酚A二缩水甘油醚)和BFDGE(双酚F二缩水甘油醚)对Caco-2细胞的体外细胞毒性作用。

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摘要

Bisphenol A diglycidyl ether (BADGE) and bisphenol F diglycidyl ether (BFDGE) are used as starting substances for the manufacturing of epoxy resins used in internal can coatings. They are obtained by a condensation reaction between epichlorohydrin with bisphenol A and bisphenol F, respectively. These potential endocrine disrupting chemicals are able to enter the food chain and to reach the intestinal epithelium, causing structural and functional damages. The human colorectal adenocarcinoma cell line Caco-2 is a widely used in vitro model of the intestinal cells. The aim of this study was to characterize BADGE and BFDGE toxicity in Caco-2 cells, in particular, at the cellular and molecular level. Using several approaches, we characterized BADGE- and BFDGE-induced cell toxicity in Caco-2 cells. The treatment was done using different concentrations up to cytotoxic doses and different times of exposure to the agents. We evaluated the effect of these compounds on cell morphology, cell detachment, cell proliferation, F-actin disruption and plasma membrane integrity. Both compounds are able to induce morphological changes, cell detachment from the substratum and to inhibit cell proliferation, being these effects time and dose-dependent. Moreover, BADGE and BFDGE induce F-actin depolymerization, this effect is very potent at 24 h of incubation with the agents and a complete F-actin disruption can be observed at 200 microM BADGE or BFDGE. In addition, cell integrity is not damaged, since neither propidium iodide uptake nor LDH release takes place in Caco-2 cells exposed to high doses of these agents for 24 h.
机译:双酚A二缩水甘油醚(BADGE)和双酚F二缩水甘油醚(BFDGE)用作制造罐头内部涂料用环氧树脂的原料。它们分别通过表氯醇与双酚A和双酚F的缩合反应获得。这些潜在的破坏内分泌的化学物质能够进入食物链并到达肠道上皮,从而导致结构和功能受损。人结肠直肠腺癌细胞系Caco-2是广泛使用的肠道细胞体外模型。这项研究的目的是表征Caco-2细胞中BADGE和BFDGE的毒性,特别是在细胞和分子水平。使用几种方法,我们表征了Caco-2细胞中BADGE和BFDGE诱导的细胞毒性。使用直至细胞毒性剂量的不同浓度和暴露于药剂的不同时间进行治疗。我们评估了这些化合物对细胞形态,细胞脱离,细胞增殖,F-肌动蛋白破坏和质膜完整性的影响。两种化合物都能够诱导形态变化,细胞从基质脱离以及抑制细胞增殖,这两种作用均与时间和剂量有关。此外,BADGE和BFDGE诱导F-肌动蛋白解聚,这种作用在与试剂孵育24小时后非常有效,并且在200 microM BADGE或BFDGE可以观察到F-肌动蛋白完全破坏。此外,细胞完整性没有受到损害,因为暴露于高剂量这些试剂24小时的Caco-2细胞中碘化丙锭的摄取和LDH的释放均不会发生。

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