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硒氨基酸在肠内营养治疗中通过抑制铁死亡对炎症性肠病的保护作用。

Protective role of seleno-amino acid against IBD via ferroptosis inhibition in enteral nutrition therapy.

作者信息

Huangfu Shuchen, Zheng Jie, He Jiashuai, Liao Jin, Jiang Haiping, Zhou Hua, Pan Jinghua

机构信息

Department of General Surgery, the First Affiliated Hospital of Jinan University, Guangzhou 510632, China.

Department of Food Science and Engineering, Jinan University, Guangzhou 510632, China.

出版信息

iScience. 2024 Jul 14;27(9):110494. doi: 10.1016/j.isci.2024.110494. eCollection 2024 Sep 20.

DOI:10.1016/j.isci.2024.110494
PMID:39290833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11407031/
Abstract

The interplay between intestinal barrier degradation and trace element insufficiency worsens inflammatory bowel disease (IBD). Selenium (se) is essential for glutathione peroxidase 4 (GPX4) synthesis, which protects against intestinal epithelial cell injury in IBD. However, malnutrition and malabsorption limit the availability of dietary selenium. This study investigated the protective effects of naturally occurring seleno-amino acids on the intestinal barrier in an IBD animal model by promoting GPX4 synthesis. L-se-methylselenocystine (seMc) supplementation reversed decreased GPX4 expression levels, alleviated glutathione depletion and scavenged reactive oxygen species . , enteral nutrition combined with seMc protected the intestinal barrier and alleviated IBD-related symptoms by inhibiting ferroptosis and reversing lipid peroxidation in epithelial cells while reducing immune cell infiltration. Our findings suggest that seleno-amino acid-based nutritional formulations may provide a basis for nutritional support to alleviate complex cycles between intestinal barrier damage and malnutrition in IBD patients.

摘要

肠道屏障降解与微量元素不足之间的相互作用会使炎症性肠病(IBD)恶化。硒(Se)对于谷胱甘肽过氧化物酶4(GPX4)的合成至关重要,GPX4可保护IBD患者的肠道上皮细胞免受损伤。然而,营养不良和吸收不良限制了膳食硒的可利用性。本研究通过促进GPX4合成,探讨了天然存在的硒氨基酸对IBD动物模型肠道屏障的保护作用。补充L-硒甲基硒代半胱氨酸(SeMc)可逆转GPX4表达水平的降低,减轻谷胱甘肽耗竭并清除活性氧。此外,肠内营养联合SeMc通过抑制铁死亡和逆转上皮细胞中的脂质过氧化,同时减少免疫细胞浸润,保护了肠道屏障并减轻了IBD相关症状。我们的研究结果表明,基于硒氨基酸的营养制剂可能为营养支持提供依据,以缓解IBD患者肠道屏障损伤与营养不良之间的复杂循环。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f37/11407031/7c817476056b/gr7.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f37/11407031/7c817476056b/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f37/11407031/1e24aa9d77bf/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f37/11407031/58506906b780/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f37/11407031/82227f2a3d97/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f37/11407031/86b85ea2034c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f37/11407031/8045b37ae4b3/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f37/11407031/ebcf53ab4ee7/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f37/11407031/d3a01e669561/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f37/11407031/7c817476056b/gr7.jpg

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2D Nanozymes Modulate Gut Microbiota and T-Cell Differentiation for Inflammatory Bowel Disease Management.二维纳米酶调节肠道微生物群和T细胞分化以管理炎症性肠病
Adv Healthc Mater. 2024 Feb;13(4):e2302576. doi: 10.1002/adhm.202302576. Epub 2023 Nov 15.
3
Human umbilical cord mesenchymal stem cells derived exosome shuttling mir-129-5p attenuates inflammatory bowel disease by inhibiting ferroptosis.
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J Nanobiotechnology. 2023 Jun 12;21(1):188. doi: 10.1186/s12951-023-01951-x.
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Research progress of glutathione peroxidase family (GPX) in redoxidation.谷胱甘肽过氧化物酶家族(GPX)在氧化还原中的研究进展
Front Pharmacol. 2023 Mar 2;14:1147414. doi: 10.3389/fphar.2023.1147414. eCollection 2023.
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