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首页> 外文期刊>Toxicological sciences: An official journal of the Society of Toxicology >Evaluating the Toxicity of Cigarette Whole Smoke Solutions in an Air-Liquid-Interface Human In Vitro Airway Tissue Model
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Evaluating the Toxicity of Cigarette Whole Smoke Solutions in an Air-Liquid-Interface Human In Vitro Airway Tissue Model

机译:评价卷烟整体烟雾溶液在空气液体界面人体外气道组织模型中的毒性

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摘要

Exposure to cigarette smoke causes a multitude of pathological changes leading to tissue damage and disease. Quantifying such changes in highly differentiated in vitro human tissue models may assist in evaluating the toxicity of tobacco products. In this methods development study, well-differentiated human air-liquid-interface (ALI) in vitro airway tissue models were used to assess toxicological endpoints relevant to tobacco smoke exposure. Whole mainstream smoke solutions (WSSs) were prepared from 2 commercial cigarettes (R60 and S60) that differ in smoke constituents when machine-smoked under International Organization for Standardization conditions. The airway tissue models were exposed apically to WSSs 4-h per day for 1-5 days. Cytotoxicity, tissue barrier integrity, oxidative stress, mucin secretion, and matrix metalloproteinase (MMP) excretion were measured. The treatments were not cytotoxic and had marginal effects on tissue barrier properties; however, other endpoints responded in time-and dose-dependent manners, with the R60 resulting in higher levels of response than the S60 for many endpoints. Based on the lowest effect dose, differences in response to the WSSs were observed for mucin induction and MMP secretion. Mitigation of mucin induction by cotreatment of cultures with Nacetylcysteine suggests that oxidative stress contributes to mucus hypersecretion. Overall, these preliminary results suggest that quantifying disease-relevant endpoints using ALI airway models is a potential tool for tobacco product toxicity evaluation. Additional research using tobacco samples generated under smoking machine conditions that more closely approximate human smoking patterns will inform further methods development.
机译:暴露于卷烟烟雾导致众多的病理变化导致组织损伤和疾病。量化高度分化的体外人体组织模型的这种变化可有助于评估烟草产品的毒性。在该方法中,使用良好分化的人气 - 液 - 界面(ALI)在体外气道组织模型中用于评估与烟草烟雾暴露相关的毒理学终点。整个主流烟雾解决方案(WSSS)由2个商用香烟(R60和S60)制备,当在国际标准化条件下吸烟时,烟雾成分在烟雾成分中。气道组织模型每天4-5天暴露于WSSS 4-H.测定细胞毒性,组织阻隔完整性,氧化应激,粘液分泌和基质金属蛋白酶(MMP)排泄。治疗不是细胞毒性的,对组织屏障性质有边缘效应;然而,其他端点以时间和剂量依赖的方式响应,R60的响应导致许多端点的响应程度更高。基于最低效果剂量,观察到对粘蛋白诱导和MMP分泌的响应响应响应的差异。用苯乙酰琥珀酸盐培养物的粘液诱导减轻粘液诱导表明氧化应激有助于粘液过度折杂。总体而言,这些初步结果表明,使用ALI Airway模型量化疾病相关的终点是烟草产品毒性评估的潜在工具。使用烟草样品在吸烟机械条件下产生的额外研究,更紧密的人类吸烟模式将提供信息的进一步发展。

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