Changes of metabolic parameters, antioxidant capacity, and gut microbiota in response to substitution of ferrous sulfate with iron hydroxy methionine analog chelate in weaned piglets.

IF 4.8 2区 医学 Q2 IMMUNOLOGY Frontiers in Cellular and Infection Microbiology Pub Date : 2025-02-18 eCollection Date: 2025-01-01 DOI:10.3389/fcimb.2025.1539607
Yuemeng Fu, Guohui Zhou, Yuhang Liu, Xuejun Yuan, Ning Jiao, Wenbiao Lu, Weiren Yang
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Abstract

Introduction: Previous studies have suggested that dietary organic iron offers health advantages compared to its inorganic counterpart. However, the effects of iron hydroxy methionine analog chelate (Fe-HMA) supplementation in weaned piglets have not been fully explored. Therefore, this study aimed to investigate the effects of replacing ferrous sulfate with Fe-HMA as the iron source on serum biochemistry, antioxidant capacity, and gut microbiota in weaned piglets.

Methods: One hundred and twenty weaned piglets were randomly allocated to two treatment groups. Each group contained four replicates, with 15 pigs per replicate. Piglets were fed either 100 mg Fe/kg in the form of ferrous sulfate (Fe-sulfate group) or 50 mg Fe/kg in the form of Fe-HMA (Fe-HMA group) as the iron source for 28 days.

Results and discussion: Results showed that supplementing Fe-HMA as an iron source significantly increased the levels of triglycerides and glucose in portal venous serum, albumin in both serum and portal venous serum and decreased serum low-density lipoprotein level in weaned piglets. Additionally, Fe-HMA supplementation significantly reduced serum and liver malondialdehyde levels, while increasing catalase (CAT), glutathione peroxidase (GSH-Px), total superoxide dismutase, and manganese superoxide dismutase levels in serum, as well as GSH-Px and CAT levels in the liver. Moreover, Fe-HMA regulated the intestinal microbiota composition, notably increasing the relative abundance of Proteobacteria and decreasing microbes involved in aromatic_compound_degradation. In conclusion, dietary replacing inorganic iron with Fe-HMA improved metabolic parameters and antioxidant capacity, and regulated gut microbiota composition in weaned piglets.

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用羟基蛋氨酸类似物螯合铁替代硫酸亚铁对断奶仔猪代谢参数、抗氧化能力和肠道菌群的影响
先前的研究表明,与无机铁相比,膳食中的有机铁具有健康优势。然而,在断奶仔猪中添加铁羟基蛋氨酸类似物螯合物(Fe-HMA)的效果尚未得到充分的研究。因此,本试验旨在研究以铁- hma代替硫酸亚铁作为铁源对断奶仔猪血清生化、抗氧化能力和肠道菌群的影响。方法:120头断奶仔猪随机分为2个处理组。每组设4个重复,每个重复15头猪。仔猪分别饲喂100 mg /kg硫酸亚铁(硫酸铁组)或50 mg /kg铁- hma(铁- hma组)作为铁源,饲喂28 d。结果与讨论:结果表明,添加Fe-HMA作为铁源显著提高了断奶仔猪门静脉血清甘油三酯和葡萄糖水平、血清和门静脉血清白蛋白水平,降低了血清低密度脂蛋白水平。此外,添加Fe-HMA显著降低了血清和肝脏丙二醛水平,同时提高了血清中过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GSH-Px)、总超氧化物歧化酶和锰超氧化物歧化酶水平,以及肝脏中GSH-Px和CAT水平。此外,Fe-HMA调节了肠道菌群组成,显著增加了Proteobacteria的相对丰度,减少了参与芳香化合物降解的微生物。综上所述,饲粮中以Fe-HMA替代无机铁改善了断奶仔猪的代谢参数和抗氧化能力,并调节了肠道菌群组成。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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