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A Novel Ferritin-Core Analog Is a Safe and Effective Alternative to Oral Ferrous Iron for Treating Iron Deficiency during Pregnancy in Mice.
Helman, Sheridan L; Wilkins, Sarah J; McKeating, Daniel R; Perkins, Anthony V; Cuffe, James S M; Hartel, Gunter; Faria, Nuno; Powell, Jonathan J; Anderson, Gregory J; Frazer, David M.
Afiliación
  • Helman SL; Molecular Nutrition Laboratory, QIMR Berghofer Medical Research Institute, Herston, Australia.
  • Wilkins SJ; School of Medicine, The University of Queensland, St Lucia, Australia.
  • McKeating DR; Iron Metabolism Laboratory, QIMR Berghofer Medical Research Institute, Herston, Australia.
  • Perkins AV; School of Pharmacy and Medical Sciences, Griffith University, Southport, Australia.
  • Cuffe JSM; School of Pharmacy and Medical Sciences, Griffith University, Southport, Australia.
  • Hartel G; School of Biomedical Sciences, The University of Queensland, St Lucia, Australia.
  • Faria N; Statistics Unit, QIMR Berghofer Medical Research Institute, Herston, Australia.
  • Powell JJ; Biomineral Research Group, Department of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Anderson GJ; Biomineral Research Group, Department of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Frazer DM; Iron Metabolism Laboratory, QIMR Berghofer Medical Research Institute, Herston, Australia.
J Nutr ; 152(3): 714-722, 2022 03 03.
Article en En | MEDLINE | ID: mdl-34625812
ABSTRACT

BACKGROUND:

Many women enter pregnancy with iron stores that are insufficient to maintain maternal iron balance and support fetal development and consequently, often require iron supplements. However, the side effects associated with many currently available iron supplements can limit compliance.

OBJECTIVE:

This study aimed to test the safety and efficacy of a novel nanoparticulate iron supplement, a dietary ferritin analog termed iron hydroxide adipate tartrate (IHAT), in pregnant mice.

METHODS:

Female C57BL/6 mice were maintained on either an iron-deficient or a control diet for 2 wk prior to timed mating to develop iron-deficient or iron-sufficient pregnancy models, respectively. Mice from each model were then gavaged daily with 10 mg iron/kg body weight as either IHAT or ferrous sulfate, or with water only, beginning on embryonic day (E) 4.5. Mice were killed on E18.5 and maternal iron and hematological parameters were measured. The expression of genes encoding iron transporters and oxidative stress markers in the duodenum and placenta were determined, along with hepatic expression of the gene encoding the iron regulatory hormone hepcidin and fetal iron.

RESULTS:

Oral IHAT and ferrous sulfate were equally effective at increasing maternal hemoglobin (20.2% and 16.9%, respectively) and hepatic iron (30.2% and 29.3%, respectively), as well as total fetal iron (99.7% and 83.8%, respectively), in iron-deficient pregnant mice compared with those gavaged with water only, with no change in oxidative stress markers seen with either treatment. However, there was a significant increase in the placental expression of the oxidative stress marker heme oxygenase 1 in iron-replete pregnant mice treated with ferrous sulfate when compared with iron-replete pregnant mice gavaged with IHAT (96.9%, P <0.05).

CONCLUSIONS:

IHAT has proved a safe and effective alternative to oral ferrous sulfate in mice, and it has potential for treating iron deficiency in human pregnancy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anemia Ferropénica / Deficiencias de Hierro Límite: Animals / Female / Humans / Pregnancy Idioma: En Revista: J Nutr Año: 2022 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anemia Ferropénica / Deficiencias de Hierro Límite: Animals / Female / Humans / Pregnancy Idioma: En Revista: J Nutr Año: 2022 Tipo del documento: Article País de afiliación: Australia
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