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Protective effects of deferasirox and N-acetyl-L-cysteine on iron overload-injured bone marrow

Using an iron overload mouse model, we explored the protective effect of deferasirox (DFX) and N-acetyl-L-cysteine (NAC) on injured bone marrow hematopoietic stem/progenitor cells (HSPC) induced by iron overload. Mice were intraperitoneally injected with 25 mg iron dextran every 3 days for 4 weeks t...

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Autores principales: Shen, J.C., Zhang, Y.C., Zhao, M.F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Divulgação Científica 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649863/
https://www.ncbi.nlm.nih.gov/pubmed/29069221
http://dx.doi.org/10.1590/1414-431X20176087
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author Shen, J.C.
Zhang, Y.C.
Zhao, M.F.
author_facet Shen, J.C.
Zhang, Y.C.
Zhao, M.F.
author_sort Shen, J.C.
collection PubMed
description Using an iron overload mouse model, we explored the protective effect of deferasirox (DFX) and N-acetyl-L-cysteine (NAC) on injured bone marrow hematopoietic stem/progenitor cells (HSPC) induced by iron overload. Mice were intraperitoneally injected with 25 mg iron dextran every 3 days for 4 weeks to establish an iron overload (Fe) model. DFX or NAC were co-administered with iron dextran in two groups of mice (Fe+DFX and Fe+NAC), and the function of HSPCs was then examined. Iron overload markedly decreased the number of murine HSPCs in bone marrow. Subsequent colony-forming cell assays showed that iron overload also decreased the colony forming capacity of HSPCs, the effect of which could be reversed by DFX and NAC. The bone marrow hematopoiesis damage caused by iron overload could be alleviated by DFX and NAC.
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spelling pubmed-56498632017-10-31 Protective effects of deferasirox and N-acetyl-L-cysteine on iron overload-injured bone marrow Shen, J.C. Zhang, Y.C. Zhao, M.F. Braz J Med Biol Res Research Articles Using an iron overload mouse model, we explored the protective effect of deferasirox (DFX) and N-acetyl-L-cysteine (NAC) on injured bone marrow hematopoietic stem/progenitor cells (HSPC) induced by iron overload. Mice were intraperitoneally injected with 25 mg iron dextran every 3 days for 4 weeks to establish an iron overload (Fe) model. DFX or NAC were co-administered with iron dextran in two groups of mice (Fe+DFX and Fe+NAC), and the function of HSPCs was then examined. Iron overload markedly decreased the number of murine HSPCs in bone marrow. Subsequent colony-forming cell assays showed that iron overload also decreased the colony forming capacity of HSPCs, the effect of which could be reversed by DFX and NAC. The bone marrow hematopoiesis damage caused by iron overload could be alleviated by DFX and NAC. Associação Brasileira de Divulgação Científica 2017-10-19 /pmc/articles/PMC5649863/ /pubmed/29069221 http://dx.doi.org/10.1590/1414-431X20176087 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Shen, J.C.
Zhang, Y.C.
Zhao, M.F.
Protective effects of deferasirox and N-acetyl-L-cysteine on iron overload-injured bone marrow
title Protective effects of deferasirox and N-acetyl-L-cysteine on iron overload-injured bone marrow
title_full Protective effects of deferasirox and N-acetyl-L-cysteine on iron overload-injured bone marrow
title_fullStr Protective effects of deferasirox and N-acetyl-L-cysteine on iron overload-injured bone marrow
title_full_unstemmed Protective effects of deferasirox and N-acetyl-L-cysteine on iron overload-injured bone marrow
title_short Protective effects of deferasirox and N-acetyl-L-cysteine on iron overload-injured bone marrow
title_sort protective effects of deferasirox and n-acetyl-l-cysteine on iron overload-injured bone marrow
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649863/
https://www.ncbi.nlm.nih.gov/pubmed/29069221
http://dx.doi.org/10.1590/1414-431X20176087
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