Iron Complexes with Antarctic Krill–Derived Peptides Show Superior Effectiveness to Their Original Protein–Iron Complexes in Mice with Iron Deficiency Anemia

Antarctic krill protein–iron complex and peptide–iron complex were acquired to investigate their iron bioavailability, expression of iron-regulated genes, and in vivo antioxidant capacity. Results indicated that the Antarctic krill peptide–iron complex significantly increased the hemoglobin (Hb), se...

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Published in:Nutrients
Main Authors: Shengjie Hu, Songyi Lin, Qi Feng, Xueqing He, Haowei Xu, Lei Chen, Na Sun
Format: Text
Language:English
Published: Multidisciplinary Digital Publishing Institute 2023
Subjects:
Online Access:https://doi.org/10.3390/nu15112510
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author Shengjie Hu
Songyi Lin
Qi Feng
Xueqing He
Haowei Xu
Lei Chen
Na Sun
author_facet Shengjie Hu
Songyi Lin
Qi Feng
Xueqing He
Haowei Xu
Lei Chen
Na Sun
author_sort Shengjie Hu
collection MDPI Open Access Publishing
container_issue 11
container_start_page 2510
container_title Nutrients
container_volume 15
description Antarctic krill protein–iron complex and peptide–iron complex were acquired to investigate their iron bioavailability, expression of iron-regulated genes, and in vivo antioxidant capacity. Results indicated that the Antarctic krill peptide–iron complex significantly increased the hemoglobin (Hb), serum iron (SI), and iron contents in the liver and spleen in iron-deficiency anemia (IDA) mice (p < 0.05) compared with those of the Antarctic krill protein–iron complex. Despite the gene expressions of the divalent metal transporter 1(DMT1), the transferrin (Tf), and the transferrin receptor (TfR) being better regulated by both Antarctic krill peptide–iron complex and protein–iron complex, the relative iron bioavailability of the Antarctic krill peptide–iron complex group (152.53 ± 21.05%) was significantly higher than that of the protein–iron complex group (112.75 ± 9.60%) (p < 0.05). Moreover, Antarctic krill peptide–iron complex could enhance the antioxidant enzyme activities of superoxidase dismutase (SOD) and glutathione peroxidase (GSH-Px), reduce the malondialdehyde (MDA) level in IDA mice compared with the protein–iron complex, and reduce the cell damage caused by IDA. Therefore, these results indicated that Antarctic krill peptide–iron complex could be used as a highly efficient and multifunctional iron supplement.
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spelling ftmdpi:oai:mdpi.com:/2072-6643/15/11/2510/ 2025-01-16T19:03:27+00:00 Iron Complexes with Antarctic Krill–Derived Peptides Show Superior Effectiveness to Their Original Protein–Iron Complexes in Mice with Iron Deficiency Anemia Shengjie Hu Songyi Lin Qi Feng Xueqing He Haowei Xu Lei Chen Na Sun agris 2023-05-28 application/pdf https://doi.org/10.3390/nu15112510 EN eng Multidisciplinary Digital Publishing Institute https://dx.doi.org/10.3390/nu15112510 https://creativecommons.org/licenses/by/4.0/ Nutrients; Volume 15; Issue 11; Pages: 2510 IDA mice Antarctic krill peptide–iron iron-regulated genes iron bioavailability in vivo antioxidant capacity Text 2023 ftmdpi https://doi.org/10.3390/nu15112510 2023-08-01T10:15:37Z Antarctic krill protein–iron complex and peptide–iron complex were acquired to investigate their iron bioavailability, expression of iron-regulated genes, and in vivo antioxidant capacity. Results indicated that the Antarctic krill peptide–iron complex significantly increased the hemoglobin (Hb), serum iron (SI), and iron contents in the liver and spleen in iron-deficiency anemia (IDA) mice (p < 0.05) compared with those of the Antarctic krill protein–iron complex. Despite the gene expressions of the divalent metal transporter 1(DMT1), the transferrin (Tf), and the transferrin receptor (TfR) being better regulated by both Antarctic krill peptide–iron complex and protein–iron complex, the relative iron bioavailability of the Antarctic krill peptide–iron complex group (152.53 ± 21.05%) was significantly higher than that of the protein–iron complex group (112.75 ± 9.60%) (p < 0.05). Moreover, Antarctic krill peptide–iron complex could enhance the antioxidant enzyme activities of superoxidase dismutase (SOD) and glutathione peroxidase (GSH-Px), reduce the malondialdehyde (MDA) level in IDA mice compared with the protein–iron complex, and reduce the cell damage caused by IDA. Therefore, these results indicated that Antarctic krill peptide–iron complex could be used as a highly efficient and multifunctional iron supplement. Text Antarc* Antarctic Antarctic Krill MDPI Open Access Publishing Antarctic Ida ENVELOPE(170.483,170.483,-83.583,-83.583) The Antarctic Nutrients 15 11 2510
spellingShingle IDA mice
Antarctic krill peptide–iron
iron-regulated genes
iron bioavailability
in vivo antioxidant capacity
Shengjie Hu
Songyi Lin
Qi Feng
Xueqing He
Haowei Xu
Lei Chen
Na Sun
Iron Complexes with Antarctic Krill–Derived Peptides Show Superior Effectiveness to Their Original Protein–Iron Complexes in Mice with Iron Deficiency Anemia
title Iron Complexes with Antarctic Krill–Derived Peptides Show Superior Effectiveness to Their Original Protein–Iron Complexes in Mice with Iron Deficiency Anemia
title_full Iron Complexes with Antarctic Krill–Derived Peptides Show Superior Effectiveness to Their Original Protein–Iron Complexes in Mice with Iron Deficiency Anemia
title_fullStr Iron Complexes with Antarctic Krill–Derived Peptides Show Superior Effectiveness to Their Original Protein–Iron Complexes in Mice with Iron Deficiency Anemia
title_full_unstemmed Iron Complexes with Antarctic Krill–Derived Peptides Show Superior Effectiveness to Their Original Protein–Iron Complexes in Mice with Iron Deficiency Anemia
title_short Iron Complexes with Antarctic Krill–Derived Peptides Show Superior Effectiveness to Their Original Protein–Iron Complexes in Mice with Iron Deficiency Anemia
title_sort iron complexes with antarctic krill–derived peptides show superior effectiveness to their original protein–iron complexes in mice with iron deficiency anemia
topic IDA mice
Antarctic krill peptide–iron
iron-regulated genes
iron bioavailability
in vivo antioxidant capacity
topic_facet IDA mice
Antarctic krill peptide–iron
iron-regulated genes
iron bioavailability
in vivo antioxidant capacity
url https://doi.org/10.3390/nu15112510