کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1941021 1050793 2006 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Induction of the nuclear factor HIF-1α in acetaminophen toxicity: Evidence for oxidative stress
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Induction of the nuclear factor HIF-1α in acetaminophen toxicity: Evidence for oxidative stress
چکیده انگلیسی

Hypoxia inducible factor (HIF) controls the transcription of genes involved in angiogenesis, erythropoiesis, glycolysis, and cell survival. HIF-1α levels are a critical determinant of HIF activity. The induction of HIF-1α was examined in the livers of mice treated with a toxic dose of APAP (300 mg/kg IP) and sacrificed at 1, 2, 4, 8, and 12 h. HIF-1α was induced at 1–12 h and induction occurred prior to the onset of toxicity. Pre-treatment of mice with N-acetylcysteine (1200 mg/kg IP) prevented toxicity and HIF-1α induction. In further studies, hepatocyte suspensions were incubated with APAP (1 mM) in the presence of an oxygen atmosphere. HIF-1α was induced at 1 h, prior to the onset of toxicity. Inclusion of cyclosporine A (10 μM), an inhibitor of mitochondrial permeability transition, oxidative stress, and toxicity, prevented the induction of HIF-1α. Thus, HIF-1α is induced before APAP toxicity and can occur under non-hypoxic conditions. The data suggest a role for oxidative stress in the induction of HIF-1α in APAP toxicity.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochemical and Biophysical Research Communications - Volume 343, Issue 1, 28 April 2006, Pages 171–176
نویسندگان
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