
pmid: 21685238
The majority of murine models of iron sucrose-induced iron overload were carried out in adult subjects. This cannot reflect the high risk of iron overload in children who have an increased need for iron. In this study, we developed four experimental iron overload models in young rats using iron sucrose and evaluated different markers of iron overload, tissue oxidative stress and inflammation as its consequences. Iron overload was observed in all iron-treated rats, as evidenced by significant increases in serum iron indices, expression of liver hepcidin gene and total tissue iron content compared with control rats. We also showed that total tissue iron content was mainly associated with the dose of iron whereas serum iron indices depended essentially on the duration of iron administration. However, no differences in tissue inflammatory and antioxidant parameters from controls were observed. Furthermore, only rats exposed to daily iron injection at a dose of 75 mg/kg body weight for one week revealed a significant increase in lipid peroxidation in iron-treated rats compared with their controls. The present results suggest a correlation between iron overload levels and the dose of iron, as well as the duration and frequency of iron injection and confirm that iron sucrose may not play a crucial role in inflammation and oxidative stress. This study provides important information about iron sucrose-induced iron overload in rats and may be useful for iron sucrose therapy for iron deficiency anemia as well as for the prevention and diagnosis of iron sucrose-induced iron overload in pediatric patients.
Serum, YOUNG RATS, Iron Overload, Time Factors, Iron, Gene Expression, IRON SUCROSE, 551, Ferric Compounds, HEPCIDIN, Glucaric Acid, Hepcidins, IRON OVERLOAD, Animals, Humans, Ferric Oxide, Saccharated, Inflammation, Dose-Response Relationship, Drug, TISSUE IRON CONTENT, Rats, Disease Models, Animal, Oxidative Stress, Liver, [SDV.TOX]Life Sciences [q-bio]/Toxicology, [SDE]Environmental Sciences, Lipid Peroxidation, FERRITIN, Biomarkers, Antimicrobial Cationic Peptides
Serum, YOUNG RATS, Iron Overload, Time Factors, Iron, Gene Expression, IRON SUCROSE, 551, Ferric Compounds, HEPCIDIN, Glucaric Acid, Hepcidins, IRON OVERLOAD, Animals, Humans, Ferric Oxide, Saccharated, Inflammation, Dose-Response Relationship, Drug, TISSUE IRON CONTENT, Rats, Disease Models, Animal, Oxidative Stress, Liver, [SDV.TOX]Life Sciences [q-bio]/Toxicology, [SDE]Environmental Sciences, Lipid Peroxidation, FERRITIN, Biomarkers, Antimicrobial Cationic Peptides
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 9 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
