کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5559444 1561578 2017 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Genotoxic effect and rat hepatocyte death occurred after oxidative stress induction and antioxidant gene downregulation caused by long term fluoride exposure
ترجمه فارسی عنوان
اثر ژنوتوکسیک و مرگ سلولی هپاتوستیک پس از القاء استرس اکسیداتیو و کاهش غلظت ژن آنتی اکسیدان ناشی از فلوراید بلند مدت
کلمات کلیدی
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
چکیده انگلیسی


- Prolonged intake of sodium fluoride induced genotoxicity in rat erythrocytes.
- Showed no evidence of apoptosis and mithocondrial swelling.
- Generated oxidative stress by affecting thiol homeostasis of the total proteins.
- Promoted SOD and GST downregulation.
- And caused hepatocytes death, confirming fluoride hepatotoxicity.

Studies focusing on possible genotoxic effects of excess fluoride are contradictory and inconclusive. Currently, studies have reported a probable link to oxidative stress, DNA damage and apoptosis induced by fluoride in rat hepatocytes. We developed an in vivo study administering three doses of fluoride by gavage given to rats for 60 day. Micronucleus test was applied to investigate genotoxic potential of fluoride. The TUNEL method determined DNA fragmentation and apoptosis. Biochemical parameters to investigate mitochondrial swelling and oxidative stress. Semi-quantitative RT-PCR and immunostaining to determine mRNA and protein expression of antioxidant enzymes. Analyses of the hepatic function and morphology were performed. Our results revealed the genotoxic potential of fluoride but did not confirm mitochondrial swelling nor an increase of positive TUNEL labelling induced by fluoride, indicating absence of apoptosis. Oxidative stress induction was confirmed and is probably associated to DNA damage. Cell death events such as empty nuclear spaces, cytoplasm degeneration, nuclear pyknosis, karyorrhexis and karyorrhexis followed by karyolysis were observed. Hepatic function did not appear to be significantly modified makes no evidence of necrosis and suggesting other cell death pathway, the autophagic. In conclusion, prolonged fluoride intake at chosen concentrations caused imbalance of the cellular oxidative state, affected DNA and disrupted cellular homeostasis. It is recommended that fluoride supplementation requires a fresh consideration in light of the current study.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemico-Biological Interactions - Volume 264, 25 February 2017, Pages 25-33
نویسندگان
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