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乳糜泻中特定生物活性脂质的上调。

Up-Regulation of Specific Bioactive Lipids in Celiac Disease.

机构信息

Pediatric Gastroenterology and Nutrition Unit, Hospital Regional Universitario de Malaga, 29011 Málaga, Spain.

Department of Experimental Medicine, Lleida Biomedical Research Institute (IRBLleida), University of Lleida (UdL), 25198 Lleida, Spain.

出版信息

Nutrients. 2021 Jun 30;13(7):2271. doi: 10.3390/nu13072271.

DOI:10.3390/nu13072271
PMID:34209150
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8308317/
Abstract

Celiac disease (CD) is an autoimmune enteropathy linked to alterations of metabolism. Currently, limited untargeted metabolomic studies evaluating differences in the plasma metabolome of CD subjects have been documented. We engage in a metabolomic study that analyzes plasma metabolome in 17 children with CD treated with a gluten-free diet and 17 healthy control siblings in order to recognize potential changes in metabolic networks. Our data demonstrates the persistence of metabolic defects in CD subjects in spite of the dietary treatment, affecting a minor but significant fraction (around 4%, 209 out of 4893 molecular features) of the analyzed plasma metabolome. The affected molecular species are mainly, but not exclusively, lipid species with a particular affectation of steroids and derivatives (indicating an adrenal gland affectation), glycerophospholipids (to highlight phosphatidic acid), glycerolipids (with a special affectation of diacylglycerols), and fatty acyls (eicosanoids). Our findings are suggestive of an activation of the diacylglycerol-phosphatidic acid signaling pathway in CD that may potentially have detrimental effects via activation of several targets including protein kinases such as mTOR, which could be the basis of the morbidity and mortality connected with untreated CD. However, more studies are necessary to validate this idea regarding CD.

摘要

乳糜泻(CD)是一种与代谢改变相关的自身免疫性肠病。目前,已有有限的针对 CD 患者血浆代谢组学差异的非靶向代谢组学研究被记录。我们进行了一项代谢组学研究,分析了 17 名接受无麸质饮食治疗的 CD 儿童和 17 名健康对照兄弟姐妹的血浆代谢组,以识别代谢网络中的潜在变化。我们的数据表明,尽管进行了饮食治疗,CD 患者仍存在代谢缺陷,影响了分析的血浆代谢组中一小部分但具有统计学意义的(约 4%,4893 种分子特征中的 209 种)。受影响的分子种类主要是(但不仅限于)脂质种类,类固醇及其衍生物(表明肾上腺受累)、甘油磷脂(以磷脂酸为重点)、甘油酯(特别是二酰基甘油)和脂肪酸酰基受到特别影响。我们的研究结果表明,CD 中存在二酰基甘油-磷脂酸信号通路的激活,这可能通过激活包括 mTOR 在内的多个靶标产生有害影响,mTOR 可能是与未经治疗的 CD 相关的发病率和死亡率的基础。然而,还需要更多的研究来验证这一观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9555/8308317/805ef064670e/nutrients-13-02271-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9555/8308317/fc962c9b1fc2/nutrients-13-02271-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9555/8308317/805ef064670e/nutrients-13-02271-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9555/8308317/fc962c9b1fc2/nutrients-13-02271-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9555/8308317/805ef064670e/nutrients-13-02271-g002.jpg

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本文引用的文献

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Nutrients. 2020 Dec 2;12(12):3723. doi: 10.3390/nu12123723.
2
New Era of Diacylglycerol Kinase, Phosphatidic Acid and Phosphatidic Acid-Binding Protein.二酰基甘油激酶、磷酸脂酸和磷酸脂酸结合蛋白的新纪元。
Int J Mol Sci. 2020 Sep 16;21(18):6794. doi: 10.3390/ijms21186794.
3
mTOR sustains inflammatory response in celiac disease.mTOR 在乳糜泻中维持炎症反应。
儿童乳糜泻的代谢组学分析:超越无麸质饮食。
Nutrients. 2023 Jun 25;15(13):2871. doi: 10.3390/nu15132871.
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Cord serum metabolic signatures of future progression to immune-mediated diseases.未来进展为免疫介导疾病的脐带血血清代谢特征。
iScience. 2023 Feb 25;26(3):106268. doi: 10.1016/j.isci.2023.106268. eCollection 2023 Mar 17.
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Lipids in Liver Failure Syndromes: A Focus on Eicosanoids, Specialized Pro-Resolving Lipid Mediators and Lysophospholipids.肝衰竭综合征中的脂质:聚焦类二十烷酸、特异性促解决脂质介质和溶血磷脂。
Front Immunol. 2022 Mar 31;13:867261. doi: 10.3389/fimmu.2022.867261. eCollection 2022.
Sci Rep. 2020 Jul 1;10(1):10798. doi: 10.1038/s41598-020-67889-4.
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Using MetaboAnalyst 4.0 for Comprehensive and Integrative Metabolomics Data Analysis.使用MetaboAnalyst 4.0进行全面综合的代谢组学数据分析。
Curr Protoc Bioinformatics. 2019 Dec;68(1):e86. doi: 10.1002/cpbi.86.
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