Iron-Induced Liver Injury: A Critical Reappraisal

被引:55
作者
Bloomer, Steven A. [1 ]
Brown, Kyle E. [2 ,3 ,4 ]
机构
[1] Penn State Univ, Abington Coll, Div Sci & Engn, Abington, PA 19001 USA
[2] Iowa City Vet Adm Med Ctr, Iowa City, IA 52242 USA
[3] Univ Iowa, Roy J & Lucille A Carver Coll Med, Div Gastroenterol Hepatol, Iowa City, IA 52242 USA
[4] Univ Iowa, Roy J & Lucille A Carver Coll Med, Program Free Radical & Radiat Biol, Iowa City, IA 52242 USA
关键词
chelation; cirrhosis; hemochromatosis; iron; liver injury; phlebotomy; CHRONIC HEPATITIS-C; TRANSFERRIN-BOUND IRON; INDUCED LIPID-PEROXIDATION; GROWTH-FACTOR-BETA; NF-KAPPA-B; DIETARY IRON; OXIDATIVE STRESS; LONG-TERM; RAT-LIVER; ANIMAL-MODEL;
D O I
10.3390/ijms20092132
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Iron is implicated in the pathogenesis of a number of human liver diseases. Hereditary hemochromatosis is the classical example of a liver disease caused by iron, but iron is commonly believed to contribute to the progression of other forms of chronic liver disease such as hepatitis C infection and nonalcoholic fatty liver disease. In this review, we present data from cell culture experiments, animal models, and clinical studies that address the hepatotoxicity of iron. These data demonstrate that iron overload is only weakly fibrogenic in animal models and rarely causes serious liver damage in humans, calling into question the concept that iron overload is an important cause of hepatotoxicity. In situations where iron is pathogenic, iron-induced liver damage may be potentiated by coexisting inflammation, with the resulting hepatocyte necrosis an important factor driving the fibrogenic response. Based on the foregoing evidence that iron is less hepatotoxic than is generally assumed, claims that assign a causal role to iron in liver injury in either animal models or human liver disease should be carefully evaluated.
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页数:21
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