التفاصيل البيبلوغرافية
| العنوان: |
Acute Acetaminophen Intoxication Leads to Hepatic Iron Loading by Decreased Hepcidin Synthesis. |
| المؤلفون: |
van Swelm, Rachel P. L.1, Laarakkers, Coby M. M.2, Blous, Linda1, Peters, Janny G. P.1, Davidson, Esmeralda N. Blaney3, van der Kraan, Peter M.3, Swinkels, Dorine W.2, Masereeuw, Rosalinde1, Russel, Frans G. M.1 |
| المصدر: |
Toxicological Sciences. Sep2012, Vol. 129 Issue 1, p225-233. 9p. 1 Diagram, 2 Charts, 4 Graphs. |
| مصطلحات موضوعية: |
*ACETAMINOPHEN, *TEMPERANCE, *HEPCIDIN, *LIVER injuries, *DRUG side effects, *OXIDATIVE stress, *ERYTHROPOIETIN, *CELLULAR signal transduction |
| مستخلص: |
Acetaminophen (APAP), a major cause of acute liver injury in the Western world, is mediated by metabolism and oxidative stress. Recent studies have suggested a role for iron in potentiating APAP-induced liver injury although its regulatory mechanism is not completely understood. The current study was designed to unravel the iron-regulating pathways in mice after APAP-induced hepatotoxicity. Mice with severe injury showed a significant increase in liver iron concentration and oxidative stress. Concurrently, the plasma concentration of hepcidin, the key regulator in iron metabolism, and hepatic hepcidin antimicrobial peptide (Hamp) mRNA expression levels were significantly reduced. We showed that hepcidin transcription was inhibited via several hepcidin-regulating factors, including the bone morphogenetic protein/small mother against decapentaplegic (BMP/SMAD) pathway, CCAAT/enhancer-binding protein α (C/EBPα), and possibly also via erythropoietin (EPO). Downregulation of the BMP/SMAD signaling pathway was most likely caused by hypoxia-inducible factor 1α (HIF-1α), which was increased in mice with severe APAP-induced liver injury. HIF-1α stimulates cleaving of hemojuvelin, the cofactor of the BMP receptor, thereby blocking BMP-induced signaling. In addition, gene expression levels of C/ebpα were significantly reduced, and Epo mRNA expression levels were significantly increased after APAP intoxication. These factors are regulated through HIF-1α during oxidative stress and suggest that HIF-1α is a key modulator in reduced hepcidin transcription after APAP-induced hepatotoxicity. In conclusion, acute APAP-induced liver injury leads to activation of HIF-1α, which results in a downregulation in hepcidin expression through a BMP/SMAD signaling pathway and through C/EBPα inhibition. Eventually, this leads to hepatic iron loading associated with APAP cytotoxicity. [ABSTRACT FROM PUBLISHER] |
| قاعدة البيانات: |
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