二烯丙基二硫醚降低氨基甲酸乙酯诱导的肠和肝细胞的细胞毒性和凋亡。

IF 3.7 3区 医学 Q2 CHEMISTRY, MEDICINAL
Caroline Andolfato Sanchez, Estefani Maria Treviso, Cecília Cristina de Souza Rocha, Lusânia Maria Greggi Antunes
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引用次数: 0

摘要

流行病学研究表明,生活方式和饮食习惯与癌症发病率上升有关。食用发酵食品和酒精饮料以及吸烟可使人类暴露于氨基甲酸乙酯(EC),这是一种可能的人类致癌物,被国际癌症研究机构(IARC)列为2A类。增加生物活性化合物的摄入可以减少ec引起的毒性。在大蒜中发现的二烯丙基二硫醚(DADS)可以防止化学试剂和天然化合物引起的损害。本研究通过评估大肠直肠癌(Caco-2)和肝癌(HepG2)细胞中EC诱导的细胞毒性、DNA损伤、细胞凋亡和活性氧的产生来研究DADS对EC的潜在保护作用。为此,采用resazurin、comet和annexin V-FITC染色法和CM-H2DCFDA标记物评价DADS (10-120 μM)和EC (80 mM)联合处理方案对Caco-2和HepG2细胞的影响。方案如下:(i)细胞用DADS预处理2 h,然后暴露于EC 24 h;(ii)用DADS预处理24小时,再用EC处理24小时的细胞;(iii)细胞同时暴露于DADS和EC 24小时;(iv)细胞暴露于EC 24 h和DADS处理2 h。EC诱导Caco-2和HepG2细胞的细胞毒性和凋亡以及Caco-2细胞的氧化损伤。在Caco-2和HepG2细胞中,DADS和EC联合暴露24小时可降低EC介导的细胞毒性和凋亡。这些发现鼓励了对DADS和EC联合作用机制的进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diallyl Disulfide Reduces Ethyl Carbamate-Induced Cytotoxicity and Apoptosis in Intestinal and Hepatic Cells.

Epidemiological studies indicate that lifestyle and dietary habits are associated with an increasing cancer incidence. Consuming fermented foods and alcoholic beverages and smoking can expose humans to ethyl carbamate (EC), a probable human carcinogen classified as group 2A by the International Agency for Research on Cancer (IARC). Increasing the intake of bioactive compounds can reduce EC-induced toxicity. Diallyl disulfide (DADS), found in garlic, may protect against damage induced by chemical agents and natural compounds. Here, the potential protective effect of DADS against EC was investigated by evaluating EC-induced cytotoxicity, DNA damage, apoptosis, and reactive oxygen species production in colorectal adenocarcinoma (Caco-2) and hepatocarcinoma (HepG2) cells. To this end, resazurin, comet, and annexin V-FITC staining assays and CM-H2DCFDA markers were used to evaluate the effect on Caco-2 and HepG2 cells of protocols combining DADS (10-120 μM) and EC (80 mM). The protocols were as follows: (i) cells pretreated with DADS for 2 h and exposed to EC for 24 h; (ii) cells pretreated with DADS for 24 h and exposed to EC for 24 h; (iii) cells simultaneously exposed to DADS and EC for 24 h; (iv) cells exposed to EC for 24 h and treated with DADS for 2 h. EC induced cytotoxicity and apoptosis in Caco-2 and HepG2 cells and oxidative damage in Caco-2 cells. Combined exposure to DADS and EC for 24 h decreased EC-mediated cytotoxicity and apoptosis in both Caco-2 and HepG2 cells. These findings encourage further studies on the mechanisms of action of the combined DADS and EC.

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来源期刊
CiteScore
7.90
自引率
7.30%
发文量
215
审稿时长
3.5 months
期刊介绍: Chemical Research in Toxicology publishes Articles, Rapid Reports, Chemical Profiles, Reviews, Perspectives, Letters to the Editor, and ToxWatch on a wide range of topics in Toxicology that inform a chemical and molecular understanding and capacity to predict biological outcomes on the basis of structures and processes. The overarching goal of activities reported in the Journal are to provide knowledge and innovative approaches needed to promote intelligent solutions for human safety and ecosystem preservation. The journal emphasizes insight concerning mechanisms of toxicity over phenomenological observations. It upholds rigorous chemical, physical and mathematical standards for characterization and application of modern techniques.
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