Clinically approved iron chelators influence zebrafish mortality, hatching morphology and cardiac function.

Iron chelation therapy using iron (III) specific chelators such as desferrioxamine (DFO, Desferal), deferasirox (Exjade or ICL-670), and deferiprone (Ferriprox or L1) are the current standard of care for the treatment of iron overload. Although each chelator is capable of promoting some degree of ir...

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Main Authors: Jasmine L Hamilton, Azadeh Hatef, Muhammad Imran ul-Haq, Neelima Nair, Suraj Unniappan, Jayachandran N Kizhakkedathu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4199627?pdf=render
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author Jasmine L Hamilton
Azadeh Hatef
Muhammad Imran ul-Haq
Neelima Nair
Suraj Unniappan
Jayachandran N Kizhakkedathu
author_facet Jasmine L Hamilton
Azadeh Hatef
Muhammad Imran ul-Haq
Neelima Nair
Suraj Unniappan
Jayachandran N Kizhakkedathu
author_sort Jasmine L Hamilton
collection DOAJ
description Iron chelation therapy using iron (III) specific chelators such as desferrioxamine (DFO, Desferal), deferasirox (Exjade or ICL-670), and deferiprone (Ferriprox or L1) are the current standard of care for the treatment of iron overload. Although each chelator is capable of promoting some degree of iron excretion, these chelators are also associated with a wide range of well documented toxicities. However, there is currently very limited data available on their effects in developing embryos. In this study, we took advantage of the rapid development and transparency of the zebrafish embryo, Danio rerio to assess and compare the toxicity of iron chelators. All three iron chelators described above were delivered to zebrafish embryos by direct soaking and their effects on mortality, hatching and developmental morphology were monitored for 96 hpf. To determine whether toxicity was specific to embryos, we examined the effects of chelator exposure via intra peritoneal injection on the cardiac function and gene expression in adult zebrafish. Chelators varied significantly in their effects on embryo mortality, hatching and morphology. While none of the embryos or adults exposed to DFO were negatively affected, ICL -treated embryos and adults differed significantly from controls, and L1 exerted toxic effects in embryos alone. ICL-670 significantly increased the mortality of embryos treated with doses of 0.25 mM or higher and also affected embryo morphology, causing curvature of larvae treated with concentrations above 0.5 mM. ICL-670 exposure (10 µL of 0.1 mM injection) also significantly increased the heart rate and cardiac output of adult zebrafish. While L1 exposure did not cause toxicity in adults, it did cause morphological defects in embryos at 0.5 mM. This study provides first evidence on iron chelator toxicity in early development and will help to guide our approach on better understanding the mechanism of iron chelator toxicity.
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spelling doaj.art-a61afbb7a0284a7c94dce51a038b07d12022-12-21T20:31:55ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01910e10988010.1371/journal.pone.0109880Clinically approved iron chelators influence zebrafish mortality, hatching morphology and cardiac function.Jasmine L HamiltonAzadeh HatefMuhammad Imran ul-HaqNeelima NairSuraj UnniappanJayachandran N KizhakkedathuIron chelation therapy using iron (III) specific chelators such as desferrioxamine (DFO, Desferal), deferasirox (Exjade or ICL-670), and deferiprone (Ferriprox or L1) are the current standard of care for the treatment of iron overload. Although each chelator is capable of promoting some degree of iron excretion, these chelators are also associated with a wide range of well documented toxicities. However, there is currently very limited data available on their effects in developing embryos. In this study, we took advantage of the rapid development and transparency of the zebrafish embryo, Danio rerio to assess and compare the toxicity of iron chelators. All three iron chelators described above were delivered to zebrafish embryos by direct soaking and their effects on mortality, hatching and developmental morphology were monitored for 96 hpf. To determine whether toxicity was specific to embryos, we examined the effects of chelator exposure via intra peritoneal injection on the cardiac function and gene expression in adult zebrafish. Chelators varied significantly in their effects on embryo mortality, hatching and morphology. While none of the embryos or adults exposed to DFO were negatively affected, ICL -treated embryos and adults differed significantly from controls, and L1 exerted toxic effects in embryos alone. ICL-670 significantly increased the mortality of embryos treated with doses of 0.25 mM or higher and also affected embryo morphology, causing curvature of larvae treated with concentrations above 0.5 mM. ICL-670 exposure (10 µL of 0.1 mM injection) also significantly increased the heart rate and cardiac output of adult zebrafish. While L1 exposure did not cause toxicity in adults, it did cause morphological defects in embryos at 0.5 mM. This study provides first evidence on iron chelator toxicity in early development and will help to guide our approach on better understanding the mechanism of iron chelator toxicity.http://europepmc.org/articles/PMC4199627?pdf=render
spellingShingle Jasmine L Hamilton
Azadeh Hatef
Muhammad Imran ul-Haq
Neelima Nair
Suraj Unniappan
Jayachandran N Kizhakkedathu
Clinically approved iron chelators influence zebrafish mortality, hatching morphology and cardiac function.
PLoS ONE
title Clinically approved iron chelators influence zebrafish mortality, hatching morphology and cardiac function.
title_full Clinically approved iron chelators influence zebrafish mortality, hatching morphology and cardiac function.
title_fullStr Clinically approved iron chelators influence zebrafish mortality, hatching morphology and cardiac function.
title_full_unstemmed Clinically approved iron chelators influence zebrafish mortality, hatching morphology and cardiac function.
title_short Clinically approved iron chelators influence zebrafish mortality, hatching morphology and cardiac function.
title_sort clinically approved iron chelators influence zebrafish mortality hatching morphology and cardiac function
url http://europepmc.org/articles/PMC4199627?pdf=render
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