کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2598823 1133151 2015 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Cytotoxic effects and degradation products of three mycotoxins: Alternariol, 3-acetyl-deoxynivalenol and 15-acetyl-deoxynivalenol in liver hepatocellular carcinoma cells
ترجمه فارسی عنوان
اثرات سیتوتوکسیک و محصولات تخریب سه میکروکوزین: اورتاناریول، 3-استیل دیوکسیینوالنول و 15-استیلدئوکسینوالنول در سلولهای کارسینوم هپاتوسلولار کبدی
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
چکیده انگلیسی


• IC50 values on HepG2 revealed that DON’s derivated presented the highest toxicity.
• Mycotoxin remaining in media: initially increases and afterward decreases.
• Relative abundance for AOH and 3-ADON’s gluthathione ion products was similar.

This work is focused in studying the cytotoxic effects on HepG2 cells of the mycotoxins alternariol (AOH), 3-acetyl-deoxynivalenol (3-ADON) and 15-acetyl-deoxynivalenol (15-ADON) by the MTT assay, as well as in the identification of the degradation products and/or metabolites originated after treatment by liquid chromatography tandem mass spectrometry (LC–MS/MS) equipment and extracted from culture media. HepG2 cells were treated at different concentrations over 24, 48 and 72 h. The IC50 values were from 65 to 96 μM, from 3.6 to 6.2 μM and from 5.2 to 8.1 μM for AOH, 3-ADON and 15-ADON, respectively. Among all three mycotoxins assayed, deoxynivalenol (DON) derivated presented the highest toxic potential. Mass spectrometry (MS) scan chromatograms of studied mycotoxins allowed to detect products from: (i) the glutathione conjugate: (ii) sulfuric acid conjugated and (iii) amino group of cysteine conjugate. At all assayed times, the increase of recoveries values was obtained in a concentration dependent manner to finally decrease in the following ranking: 72 h > 24 h > 48 h. The abundance relative (%) obtained for AOH’s gluthathione ion product oscillated between 48 and 80% while for 3-ADON’s ranged from 50 to 80%.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Toxicology Letters - Volume 235, Issue 1, 19 May 2015, Pages 8–16
نویسندگان
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