Curcumin may impair iron status when fed to mice for six months
| العنوان: | Curcumin may impair iron status when fed to mice for six months |
|---|---|
| المؤلفون: | Patricia Huebbe, Jan Frank, Kathrin Pallauf, Dawn Chin, Gerald Rimbach |
| المصدر: | Redox Biology, Vol 2, Iss C, Pp 563-569 (2014) Redox Biology |
| بيانات النشر: | Elsevier, 2014. |
| سنة النشر: | 2014 |
| مصطلحات موضوعية: | Clinical Biochemistry, TBS, tris buffered saline, Pharmacology, Biochemistry, chemistry.chemical_compound, Mice, TfR1, transferrin receptor 1, Enlarged spleen, lcsh:QH301-705.5, HO1, haem oxygenase, lcsh:R5-920, biology, qRT-PCR, quantitative real-time polymerase chain reaction, Iron deficiency, γ-GCS, γ-glutamyl cysteine synthetase, NRF2, nuclear factor (erythroid-derived 2)-like 2, Zinc, medicine.anatomical_structure, Liver, FPN, ferroportin, TNFα, tumour necrosis factor α, Toxicity, Female, Safety, lcsh:Medicine (General), Research Paper, Curcumin, Liver minerals, Iron, Spleen, Transferrin receptor, NQO1, NAD(P)H quinone oxidoreductase, Drug Administration Schedule, DMT1, divalent metal transporter 1, Hepcidins, Hepcidin, medicine, Animals, Dose-Response Relationship, Drug, Organic Chemistry, Body Weight, DMT1, medicine.disease, Iron store, IL, interleukin, Ferritin, Mice, Inbred C57BL, chemistry, Gene Expression Regulation, lcsh:Biology (General), Immunology, Dietary Supplements, Ferritins, Splenomegaly, biology.protein, Copper |
| الوصف: | Curcumin has been shown to have many potentially health beneficial properties in vitro and in animal models with clinical studies on the toxicity of curcumin reporting no major side effects. However, curcumin may chelate dietary trace elements and could thus potentially exert adverse effects. Here, we investigated the effects of a 6 month dietary supplementation with 0.2% curcumin on iron, zinc, and copper status in C57BL/6J mice. Compared to non-supplemented control mice, we observed a significant reduction in iron, but not zinc and copper stores, in the liver and the spleen, as well as strongly suppressed liver hepcidin and ferritin expression in the curcumin-supplemented mice. The expression of the iron-importing transport proteins divalent metal transporter 1 and transferrin receptor 1 was induced, while hepatic and splenic inflammatory markers were not affected in the curcumin-fed mice. The mRNA expression of other putative target genes of curcumin, including the nuclear factor (erythroid-derived 2)-like 2 and haem oxygenase 1 did not differ between the groups. Most of the published animal trials with curcumin-feeding have not reported adverse effects on iron status or the spleen. However, it is possible that long-term curcumin supplementation and a Western-type diet may aggravate iron deficiency. Therefore, our findings show that further studies are needed to evaluate the effect of curcumin supplementation on iron status. Graphical abstract A 6 month dietary supplementation with 0.2% curcumin in C57BL/6J mice led to a significant reduction in iron, but not zinc and copper stores, in the liver and the spleen, and suppressed liver hepcidin and ferritin expression. Furthermore, the expression of the iron-importing transport proteins divalent metal transporter (DMT) 1 and transferrin receptor (TfR) 1 was induced in the curcumin-fed mice. These data suggest that long-term curcumin supplementation and a Western-type diet may aggravate iron deficiency. Highlights • 0.2% dietary curcumin for 6 months reduced iron stores in murine liver and spleen. • Curcumin chelated iron but not zinc and copper in vivo. • Liver hepcidin and ferritin expression was strongly suppressed in curcumin-fed mice. • Curcumin induced expression of hepatic iron transporters DMT1 and TfR1. • Curcumin did not affect hepatic and splenic inflammatory and oxidative markers. |
| اللغة: | English |
| تدمد: | 2213-2317 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34111eb52cef8c02b7b58ec3fd7d6591Test http://www.sciencedirect.com/science/article/pii/S2213231714000330Test |
| حقوق: | OPEN |
| رقم الانضمام: | edsair.doi.dedup.....34111eb52cef8c02b7b58ec3fd7d6591 |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 22132317 |
|---|