کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4453702 1620812 2016 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
In vitro evaluation of inorganic and methyl mercury mediated cytotoxic effect on neural cells derived from different animal species
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست علوم زیست محیطی (عمومی)
پیش نمایش صفحه اول مقاله
In vitro evaluation of inorganic and methyl mercury mediated cytotoxic effect on neural cells derived from different animal species
چکیده انگلیسی

To extend the current understanding of the mercury-mediated cytotoxic effect, five neural cell lines established from different animal species were comparatively analyzed using three different endpoint bioassays: thiazolyl blue tetrazolium bromide, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay (MTT), neutral red uptake assay (NRU), and Coomassie blue assay (CB). Following a 24-hr exposure to selected concentrations of mercury chloride (HgCl2) and methylmercury (II) chloride (MeHgCl), the cytotoxic effect on test cells was characterized by comparing their 50% inhibition concentration (IC50) values. Experimental results indicated that both these forms of mercury were toxic to all the neural cells, but at very different degrees. The IC50 values of MeHgCl among these cell lines ranged from 1.15 ± 0.22 to 10.31 ± 0.70 μmol/L while the IC50 values for HgCl2 were much higher, ranging from 6.44 ± 0.36 to 160.97 ± 19.63 μmol/L, indicating the more toxic nature of MeHgCl. The IC50 ratio between HgCl2 and MeHgCl ranged from 1.75 to 96.0, which confirms that organic mercury is much more toxic to these neural cells than inorganic mercury. Among these cell lines, HGST-BR and TriG44 derived from marine sea turtles showed a significantly high tolerance to HgCl2 as compared to the three mammalian neural cells. Among these neural cells, SK-N-SH represented the most sensitive cells to both chemical forms of mercury.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Environmental Sciences - Volume 41, March 2016, Pages 138–145
نویسندگان
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