کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5559662 1561692 2017 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Nrf2 is crucial for the down-regulation of Cyp7a1 induced by arachidonic acid in Hepg2 cells
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
پیش نمایش صفحه اول مقاله
Nrf2 is crucial for the down-regulation of Cyp7a1 induced by arachidonic acid in Hepg2 cells
چکیده انگلیسی


- Nrf2 was increased dose-dependently in increasing concentrations of AA treated cell.
- CYP7A1 was decreased dose-dependently in increasing concentrations of AA treated cell.
- CYP7A1 expression was increased in Nrf2 silenced cells with AA administration.
- CYP7A1 expression was decreased in Nrf2 over-expressed cells with AA administration.
- Nrf2 plays crucial role in the down-regulation of CYP7A1 induced by AA in HepG2 cells.

In former research, cyp7a1 expression was decreased but Nrf2 transcription and hepatic arachidonic acid (AA) concentration were increased in high-fat diet fed mice. This study aims to investigate the influence of AA in CYP7A1 expression and the role of Nrf2 in regulating CYP7A1 in the process. HepG2 cells were administered with different concentrations of AA. Nrf2 and CYP7A1 expressions were analyzed by real-time PCR and western blot. Nrf2 silenced and over-expressed cell models were constructed by Nrf2 siRNA and eukaryotic expression vector transient transfections and were used to investigate the role of Nrf2 in regulating CYP7A1 following AA administration. The results showed that Nrf2 was increased dose-dependently but CYP7A1 was decreased dose-dependently in cells treated with increasing concentrations of AA. The expression of CYP7A1 was increased by Nrf2 silence and was decreased by Nrf2 over-expression in HepG2 cells treated with different concentrations of AA. In conclusion, Nrf2 plays a significant role in the down-regulation of CYP7A1 induced by AA in HepG2 cells.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Environmental Toxicology and Pharmacology - Volume 52, June 2017, Pages 21-26
نویسندگان
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