کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
9034654 | 1132631 | 2005 | 12 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Interference of arachidonic acid and its metabolites with TNF-α release by ochratoxin A from rat liver
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کلمات کلیدی
موضوعات مرتبط
علوم زیستی و بیوفناوری
علوم محیط زیست
بهداشت، سم شناسی و جهش زایی
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چکیده انگلیسی
We investigated the role of arachidonic acid and its metabolites on the ochratoxin A (OTA) provoked release of proinflammatory and apoptotic cytokine TNF-α from blood-free perfused rat liver. OTA induced TNF-α release dose- and time-dependently yielding 2600 pg TNF-α/ml at 2.5 μmol/l after 90 min without significant release of LDH and lactate. Aristolochic acid, 50 μmol/l, a phospholipase A2 inhibitor, and 10 μmol/l of exogenous arachidonic acid decreased TNF-α below normal level. Indomethacin, 10 μmol/l, a potent inhibitor of the cyclooxygenase (COX) pathway, almost doubled TNF-α concentrations in the perfusion solution to reach 5500 pg/ml at 90 min. On the other hand, inhibition of lipoxgenase (LPX) by 30 μmol/l nordihydroguaiaretic acid (NDGA) and the cytochrome P-450 (CYP) pathway by 100 μmol/l of metyrapone decreased TNF-α below normal levels as well. Concurrent administration of two blockers (COX inhibitor with LPX inhibitor, or COX inhibitor with CYP-450 inhibitor, or LPX inhibitor with CYP-450 inhibitor) blocked TNF-α release below normal levels. In addition, 10 μmol/l caffeic acid phenylethyl ester, a NF-κB inhibitor, blocked OTA mediated TNF-α release. In conclusion, arachidonic acid and its cyclooxygenase metabolites are suppressors of OTA mediated TNF-α release from liver, whereas LPX and CYP-450-metabolites have the opposite effect. OTA-induced TNF-α release is likely to occur via the NF-κB transcription factor pathway in perfused rat liver.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Toxicology - Volume 208, Issue 3, 30 March 2005, Pages 335-346
Journal: Toxicology - Volume 208, Issue 3, 30 March 2005, Pages 335-346
نویسندگان
L. AL-Anati, N. Katz, E. Petzinger,