کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8552879 | 1562278 | 2018 | 31 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
PCB95 and PCB153 change dopamine levels and turn-over in PC12 cells
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
کلمات کلیدی
3,4-dihydroxyphenylethanolDOPETPCB153PCB2,2′,4,4′,5,5′-hexachlorobiphenylPC12GPXVMATMAODOPAC3,4-dihydroxyphenylacetaldehyde - 3،4-دی هیدروکسی فنیل آستالالدئید3,4-dihydroxyphenylacetic acid - 3،4-دی هیدروکسی فنیل اسیدهای اسیدl-3,4-dihydroxyphenylalanine - L-3،4-دی هیدروکسی فنیل آلانینl-DOPA - L-DOPAROS - ROSattention deficit hyperactivity disorder - اختلال کمتوجّهی _ بیشفعالیADHD - بیشفعالیPolychlorinated biphenyl - بیفنیل پلی کربناتDopamine - دوپامینrat pheochromocytoma cell line - سلول فوکو مروسیتوم موش صحراییPC12 cells - سلول های PC12DOPAL - عصبانی کردنmonoamine oxidase - مونوآمین اکسیدازها Reactive oxygen species - گونههای فعال اکسیژن
موضوعات مرتبط
علوم زیستی و بیوفناوری
علوم محیط زیست
بهداشت، سم شناسی و جهش زایی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Polychlorinated biphenyls (PCB) exposure at low chronic levels is a significant public health concern. Animal and epidemiological studies indicate that low PCB body burden may cause neurotoxicity and be a risk factor for neurodegenerative diseases. In the current study, we measured the ability of two non-dioxin like PCBs, 2,2â²,4,4â²,5,5â²-hexachlorobiphenyl (PCB153) and 2,2â²3,5â²,6-pentachlorobiphenyl (PCB95), to alter dopamine (DA) levels and metabolism using the dopaminergic PC12 cell line. Our hypothesis is that treatment of PC12 cells with non-toxic concentrations of PCB153 or PCB95 for 12 and 24â¯h will have different effects due to different congener structures. Levels of DA and of 3,4-dihydroxyphenylacetaldehyde (DOPAL), 3, 4-dihyroxylphenylethanol (DOPET), and 3,4-dihyroxylphenylacetic acid (DOPAC) metabolite, gene expression of the dopamine synthesis enzyme tyrosine hydroxylase (TH) and the vesicular monoamine transporter (VMAT2), and gene expression of the anti-oxidant enzymes Cu/Zn and Mn superoxide oxidase (Cu/ZnSOD, MnSOD), glutathione peroxidase (GPx) and catalase were determined. PCB153 decreased intracellular and extracellular levels of DA after 12â¯h exposure and this was consistent with an increase in DA metabolites. After 24â¯h, the level of DA in medium increased compared to the control. In contrast, PCB95 exposure increased the intracellular DA level and decreased DA in medium consistent with a down-regulation of VMAT2 expression at 12â¯h. After 24â¯h exposure, PCB95 increased DA levels in media. Expression of TH mRNA increased slightly following 12â¯h but not at 24â¯h exposure. MnSOD mRNA increased up to 6-7 fold and Cu/ZnSOD increased less than two-fold after treatment with both congeners. Catalase expression was up-regulated following 24â¯h exposure to PCB153 and PCB95, but GPx expression was down-regulated after 12â¯h exposure to PCB95 only. These results suggest that PCB153 and PCB95 are neurotoxic and affect DA turnover with structure-dependent differences between these two congeners.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Toxicology - Volume 394, 1 February 2018, Pages 93-101
Journal: Toxicology - Volume 394, 1 February 2018, Pages 93-101
نویسندگان
Sabah H. Enayah, Brigitte C. Vanle, Laurence J. Fuortes, Jonathan A. Doorn, Gabriele Ludewig,