| کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن | 
|---|---|---|---|---|
| 6382111 | 1625936 | 2015 | 30 صفحه PDF | دانلود رایگان | 
عنوان انگلیسی مقاله ISI
												Silver nanoparticles disrupt regulation of steroidogenesis in fish ovarian cells
												
											ترجمه فارسی عنوان
													نانوذرات نقره مانع تنظیم استروئیدوژنز در سلول های تخمدان ماهی می شوند 
													
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																																												کلمات کلیدی
												
											موضوعات مرتبط
												
													علوم زیستی و بیوفناوری
													علوم کشاورزی و بیولوژیک
													علوم آبزیان
												
											چکیده انگلیسی
												Despite the influx of silver nanoparticles (nAg) into the marine environment, their effects on fish reproduction remain completely unexplored. Using ovarian primary cells from marine medaka (Oryzias melastigma), in vitro studies were carried out to evaluate the effects of two differently coated nAg particles (Oleic Acid, (OA) nAg and Polyvinylpyrrolidone, (PVP) nAg) on fish ovarian tissues, using AgNO3 as a positive control. Cytotoxicity was evaluated by MTT assay and expression of key genes regulating steroidogenesis (StAR, CYP 19a, CYP 11a, 3βHSD and 20βHSD) were determined by Q-RT-PCR. EC50 values for PVP nAg, OA nAg and AgNO3 were 7.25 μg Lâ1, 924.4 μg Lâ1, and 42.0 μg Lâ1 respectively, showing that toxicity of silver was greatly enhanced in the PVP coated nano-form. Down regulation of CYP 19a was observed in both nAg and AgNO3 treatments, while down regulation of 3βHSD was only found in the OA nAg and AgNO3 treatments. For the first time, our results demonstrated that nAg can affect specific genes regulating steroidogenesis, implicating nAg as a potential endocrine disruptor.
											ناشر
												Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Aquatic Toxicology - Volume 169, December 2015, Pages 143-151
											Journal: Aquatic Toxicology - Volume 169, December 2015, Pages 143-151
نویسندگان
												Natalie Degger, Anna C.K. Tse, Rudolf S.S. Wu, 
											