Staroń Robert, Lipiński Paweł, Lenartowicz Małgorzata, Bednarz Aleksandra, Gajowiak Anna, Smuda Ewa, Krzeptowski Wojciech, Pieszka Marek, Korolonek Tamara, Hamza Iqbal, Swinkels Dorine W, Van Swelm Rachel P L, Starzyński Rafał R
Institute of Genetics and Animal Breeding PAS, Department of Molecular Biology, Jastrzębiec, Poland.
Department of Genetics and Evolution, Institute of Zoology, Jagiellonian University, Kraków, Poland.
PLoS One. 2017 Jul 13;12(7):e0181117. doi: 10.1371/journal.pone.0181117. eCollection 2017.
Heme is an efficient source of iron in the diet, and heme preparations are used to prevent and cure iron deficiency anemia in humans and animals. However, the molecular mechanisms responsible for heme absorption remain only partially characterized. Here, we employed young iron-deficient piglets as a convenient animal model to determine the efficacy of oral heme iron supplementation and investigate the pathways of heme iron absorption. The use of bovine hemoglobin as a dietary source of heme iron was found to efficiently counteract the development of iron deficiency anemia in piglets, although it did not fully rebalance their iron status. Our results revealed a concerted increase in the expression of genes responsible for apical and basolateral heme transport in the duodenum of piglets fed a heme-enriched diet. In these animals the catalytic activity of heme oxygenase 1 contributed to the release of elemental iron from the protoporphyrin ring of heme within enterocytes, which may then be transported by the strongly expressed ferroportin across the basolateral membrane to the circulation. We hypothesize that the well-recognized high bioavailability of heme iron may depend on a split pathway mediating the transport of heme-derived elemental iron and intact heme from the interior of duodenal enterocytes to the bloodstream.
血红素是饮食中铁的有效来源,血红素制剂用于预防和治疗人类及动物的缺铁性贫血。然而,负责血红素吸收的分子机制仍仅部分得到表征。在此,我们采用幼龄缺铁仔猪作为便捷的动物模型,以确定口服补充血红素铁的效果,并研究血红素铁的吸收途径。发现使用牛血红蛋白作为血红素铁的饮食来源可有效对抗仔猪缺铁性贫血的发展,尽管它并未完全恢复其铁状态。我们的结果显示,在喂食富含血红素饮食的仔猪十二指肠中,负责顶端和基底外侧血红素转运的基因表达协同增加。在这些动物中,血红素加氧酶1的催化活性有助于将血红素原卟啉环中的元素铁释放到肠细胞内,然后可通过强烈表达的铁转运蛋白跨基底外侧膜转运至循环系统。我们推测,血红素铁公认的高生物利用度可能依赖于一种分裂途径,该途径介导血红素衍生的元素铁和完整血红素从十二指肠肠细胞内部转运至血液中。