Comparative Evaluation of Sucrosomial Iron and Iron Oxide Nanoparticles as Oral Supplements in Iron Deficiency Anemia in Piglets
Iron deficiency is the most common mammalian nutritional disorder. However, among mammalian species iron deficiency anemia (IDA), occurs regularly only in pigs. To cure IDA, piglets are routinely injected with high amounts of iron dextran (FeDex), which can lead to perturbations in iron homeostasis....
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creator | Mazgaj, Rafał Lipiński, Paweł Szudzik, Mateusz Jończy, Aneta Kopeć, Zuzanna Stankiewicz, Adrian M Kamyczek, Marian Swinkels, Dorine Żelazowska, Beata Starzyński, Rafał R |
description | Iron deficiency is the most common mammalian nutritional disorder. However, among mammalian species iron deficiency anemia (IDA), occurs regularly only in pigs. To cure IDA, piglets are routinely injected with high amounts of iron dextran (FeDex), which can lead to perturbations in iron homeostasis. Here, we evaluate the therapeutic efficacy of non-invasive supplementation with Sucrosomial iron (SI), a highly bioavailable iron supplement preventing IDA in humans and mice and various iron oxide nanoparticles (IONPs). Analysis of red blood cell indices and plasma iron parameters shows that not all iron preparations used in the study efficiently counteracted IDA comparable to FeDex-based supplementation. We found no signs of iron toxicity of any tested iron compounds, as evaluated based on the measurement of several toxicological markers that could indicate the occurrence of oxidative stress or inflammation. Neither SI nor IONPs increased hepcidin expression with alterations in ferroportin (FPN) protein level. Finally, the analysis of the piglet gut microbiota indicates the individual pattern of bacterial diversity across taxonomic levels, independent of the type of supplementation. In light of our results, SI but not IONPs used in the experiment emerges as a promising nutritional iron supplement, with a high potential to correct IDA in piglets. |
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However, among mammalian species iron deficiency anemia (IDA), occurs regularly only in pigs. To cure IDA, piglets are routinely injected with high amounts of iron dextran (FeDex), which can lead to perturbations in iron homeostasis. Here, we evaluate the therapeutic efficacy of non-invasive supplementation with Sucrosomial iron (SI), a highly bioavailable iron supplement preventing IDA in humans and mice and various iron oxide nanoparticles (IONPs). Analysis of red blood cell indices and plasma iron parameters shows that not all iron preparations used in the study efficiently counteracted IDA comparable to FeDex-based supplementation. We found no signs of iron toxicity of any tested iron compounds, as evaluated based on the measurement of several toxicological markers that could indicate the occurrence of oxidative stress or inflammation. Neither SI nor IONPs increased hepcidin expression with alterations in ferroportin (FPN) protein level. Finally, the analysis of the piglet gut microbiota indicates the individual pattern of bacterial diversity across taxonomic levels, independent of the type of supplementation. In light of our results, SI but not IONPs used in the experiment emerges as a promising nutritional iron supplement, with a high potential to correct IDA in piglets.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms22189930</identifier><identifier>PMID: 34576090</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Administration, Oral ; Anemia ; Anemia, Iron-Deficiency - blood ; Anemia, Iron-Deficiency - drug therapy ; Animals ; Animals, Newborn ; Bioavailability ; Biomarkers - metabolism ; Blood ; Dextran ; Dextrans ; Dietary Supplements ; Duodenum - metabolism ; Erythrocytes ; Evaluation ; Ferric Compounds - administration & dosage ; Ferric Compounds - pharmacology ; Ferric Compounds - therapeutic use ; Ferrous Compounds - therapeutic use ; Hematology ; Hemoglobin ; Hepcidin ; Hepcidins - blood ; Hepcidins - genetics ; Hogs ; Homeostasis ; Inflammation ; Intestinal microflora ; Iron ; Iron compounds ; Iron oxides ; Magnetic Iron Oxide Nanoparticles - administration & dosage ; Magnetic Iron Oxide Nanoparticles - chemistry ; Male ; Mammals ; Microbiota ; Nanoparticles ; Nutrient deficiency ; Oxidative stress ; Physiology ; Plasma ; Proteins ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Swine ; Toxicity ; Toxicity testing</subject><ispartof>International journal of molecular sciences, 2021-09, Vol.22 (18), p.9930</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-427b6101bd255d2ba153fb7709a7e15e65d33a5a034422d3d5924845c6252fe33</citedby><cites>FETCH-LOGICAL-c412t-427b6101bd255d2ba153fb7709a7e15e65d33a5a034422d3d5924845c6252fe33</cites><orcidid>0000-0002-1040-9446 ; 0000-0001-5869-7670 ; 0000-0002-2719-6205 ; 0000-0001-6706-0882 ; 0000-0002-4333-6853</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466487/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466487/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34576090$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mazgaj, Rafał</creatorcontrib><creatorcontrib>Lipiński, Paweł</creatorcontrib><creatorcontrib>Szudzik, Mateusz</creatorcontrib><creatorcontrib>Jończy, Aneta</creatorcontrib><creatorcontrib>Kopeć, Zuzanna</creatorcontrib><creatorcontrib>Stankiewicz, Adrian M</creatorcontrib><creatorcontrib>Kamyczek, Marian</creatorcontrib><creatorcontrib>Swinkels, Dorine</creatorcontrib><creatorcontrib>Żelazowska, Beata</creatorcontrib><creatorcontrib>Starzyński, Rafał R</creatorcontrib><title>Comparative Evaluation of Sucrosomial Iron and Iron Oxide Nanoparticles as Oral Supplements in Iron Deficiency Anemia in Piglets</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Iron deficiency is the most common mammalian nutritional disorder. However, among mammalian species iron deficiency anemia (IDA), occurs regularly only in pigs. To cure IDA, piglets are routinely injected with high amounts of iron dextran (FeDex), which can lead to perturbations in iron homeostasis. Here, we evaluate the therapeutic efficacy of non-invasive supplementation with Sucrosomial iron (SI), a highly bioavailable iron supplement preventing IDA in humans and mice and various iron oxide nanoparticles (IONPs). Analysis of red blood cell indices and plasma iron parameters shows that not all iron preparations used in the study efficiently counteracted IDA comparable to FeDex-based supplementation. We found no signs of iron toxicity of any tested iron compounds, as evaluated based on the measurement of several toxicological markers that could indicate the occurrence of oxidative stress or inflammation. Neither SI nor IONPs increased hepcidin expression with alterations in ferroportin (FPN) protein level. Finally, the analysis of the piglet gut microbiota indicates the individual pattern of bacterial diversity across taxonomic levels, independent of the type of supplementation. In light of our results, SI but not IONPs used in the experiment emerges as a promising nutritional iron supplement, with a high potential to correct IDA in piglets.</description><subject>Administration, Oral</subject><subject>Anemia</subject><subject>Anemia, Iron-Deficiency - blood</subject><subject>Anemia, Iron-Deficiency - drug therapy</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Bioavailability</subject><subject>Biomarkers - metabolism</subject><subject>Blood</subject><subject>Dextran</subject><subject>Dextrans</subject><subject>Dietary Supplements</subject><subject>Duodenum - metabolism</subject><subject>Erythrocytes</subject><subject>Evaluation</subject><subject>Ferric Compounds - administration & dosage</subject><subject>Ferric Compounds - pharmacology</subject><subject>Ferric Compounds - therapeutic use</subject><subject>Ferrous Compounds - therapeutic use</subject><subject>Hematology</subject><subject>Hemoglobin</subject><subject>Hepcidin</subject><subject>Hepcidins - 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However, among mammalian species iron deficiency anemia (IDA), occurs regularly only in pigs. To cure IDA, piglets are routinely injected with high amounts of iron dextran (FeDex), which can lead to perturbations in iron homeostasis. Here, we evaluate the therapeutic efficacy of non-invasive supplementation with Sucrosomial iron (SI), a highly bioavailable iron supplement preventing IDA in humans and mice and various iron oxide nanoparticles (IONPs). Analysis of red blood cell indices and plasma iron parameters shows that not all iron preparations used in the study efficiently counteracted IDA comparable to FeDex-based supplementation. We found no signs of iron toxicity of any tested iron compounds, as evaluated based on the measurement of several toxicological markers that could indicate the occurrence of oxidative stress or inflammation. Neither SI nor IONPs increased hepcidin expression with alterations in ferroportin (FPN) protein level. 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subjects | Administration, Oral Anemia Anemia, Iron-Deficiency - blood Anemia, Iron-Deficiency - drug therapy Animals Animals, Newborn Bioavailability Biomarkers - metabolism Blood Dextran Dextrans Dietary Supplements Duodenum - metabolism Erythrocytes Evaluation Ferric Compounds - administration & dosage Ferric Compounds - pharmacology Ferric Compounds - therapeutic use Ferrous Compounds - therapeutic use Hematology Hemoglobin Hepcidin Hepcidins - blood Hepcidins - genetics Hogs Homeostasis Inflammation Intestinal microflora Iron Iron compounds Iron oxides Magnetic Iron Oxide Nanoparticles - administration & dosage Magnetic Iron Oxide Nanoparticles - chemistry Male Mammals Microbiota Nanoparticles Nutrient deficiency Oxidative stress Physiology Plasma Proteins RNA, Messenger - genetics RNA, Messenger - metabolism Swine Toxicity Toxicity testing |
title | Comparative Evaluation of Sucrosomial Iron and Iron Oxide Nanoparticles as Oral Supplements in Iron Deficiency Anemia in Piglets |
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