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Interactions between arsenic exposure, high-fat diet and NRF2 shape the complex responses in the murine gut microbiome and hepatic metabolism.砷暴露、高脂饮食与NRF2之间的相互作用塑造了小鼠肠道微生物群和肝脏代谢中的复杂反应。
Front Microbiomes. 2022;1. doi: 10.3389/frmbi.2022.1041188. Epub 2022 Nov 23.
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Metabolic Phenotype of Wild-Type and -Knockout C57BL/6J Mice Exposed to Inorganic Arsenic: The Role of Dietary Fat and Folate Intake.暴露于无机砷的野生型和敲除型 C57BL/6J 小鼠的代谢表型:膳食脂肪和叶酸摄入的作用。
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Gut microbiota perturbations and neurodevelopmental impacts in offspring rats concurrently exposure to inorganic arsenic and fluoride.无机砷和氟化物同时暴露对子代大鼠肠道微生物群扰动和神经发育影响。
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引用本文的文献

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A high-fat diet exacerbates arsenic toxicity in various organs. A systematic review of toxicity and mechanism.高脂饮食会加剧砷对各个器官的毒性。毒性与作用机制的系统综述。
Curr Res Toxicol. 2025 Jul 16;9:100250. doi: 10.1016/j.crtox.2025.100250. eCollection 2025.

本文引用的文献

1
Developmental arsenic exposure induces dysbiosis of gut microbiota and disruption of plasma metabolites in mice.发育性砷暴露会导致小鼠肠道微生物群落失调和血浆代谢物紊乱。
Toxicol Appl Pharmacol. 2022 Sep 1;450:116174. doi: 10.1016/j.taap.2022.116174. Epub 2022 Jul 22.
2
Probiotics and gut microbiome - Prospects and challenges in remediating heavy metal toxicity.益生菌和肠道微生物组——修复重金属毒性的前景与挑战。
J Hazard Mater. 2021 Oct 15;420:126676. doi: 10.1016/j.jhazmat.2021.126676. Epub 2021 Jul 17.
3
Changes in Microbial Community Composition Related to Sex and Colon Cancer by Nrf2 Knockout.Nrf2 基因敲除与性别和结肠癌相关的微生物群落组成变化。
Front Cell Infect Microbiol. 2021 Jun 23;11:636808. doi: 10.3389/fcimb.2021.636808. eCollection 2021.
4
Non-canonical NRF2 activation promotes a pro-diabetic shift in hepatic glucose metabolism.非规范 NRF2 激活促进肝葡萄糖代谢向促糖尿病状态转变。
Mol Metab. 2021 Sep;51:101243. doi: 10.1016/j.molmet.2021.101243. Epub 2021 Apr 30.
5
The gut microbiome and arsenic-induced disease-iAs metabolism in mice.肠道微生物组与小鼠砷诱导疾病-无机砷代谢。
Curr Environ Health Rep. 2021 Jun;8(2):89-97. doi: 10.1007/s40572-021-00305-9. Epub 2021 Apr 14.
6
Imidazole propionate is increased in diabetes and associated with dietary patterns and altered microbial ecology.丙酸咪唑在糖尿病中增加,并与饮食模式和微生物生态的改变有关。
Nat Commun. 2020 Nov 18;11(1):5881. doi: 10.1038/s41467-020-19589-w.
7
Gut Microbiota as a Trigger for Metabolic Inflammation in Obesity and Type 2 Diabetes.肠道微生物群作为肥胖和 2 型糖尿病代谢性炎症的触发因素。
Front Immunol. 2020 Oct 16;11:571731. doi: 10.3389/fimmu.2020.571731. eCollection 2020.
8
The Relationship between Choline Bioavailability from Diet, Intestinal Microbiota Composition, and Its Modulation of Human Diseases.饮食中胆碱的生物利用度与其对肠道微生物组成的关系,及其对人类疾病的调节作用。
Nutrients. 2020 Aug 5;12(8):2340. doi: 10.3390/nu12082340.
9
The Genus : Gut Bacteria With Emerging Implications to Inflammation, Cancer, and Mental Health.属:具有潜在炎症、癌症和精神健康影响的肠道细菌。
Front Immunol. 2020 Jun 9;11:906. doi: 10.3389/fimmu.2020.00906. eCollection 2020.
10
The Firmicutes/Bacteroidetes Ratio: A Relevant Marker of Gut Dysbiosis in Obese Patients?厚壁菌门/拟杆菌门比值:肥胖患者肠道菌群失调的相关标志物?
Nutrients. 2020 May 19;12(5):1474. doi: 10.3390/nu12051474.

砷暴露、高脂饮食与NRF2之间的相互作用塑造了小鼠肠道微生物群和肝脏代谢中的复杂反应。

Interactions between arsenic exposure, high-fat diet and NRF2 shape the complex responses in the murine gut microbiome and hepatic metabolism.

作者信息

Schiro Gabriele, Liu Pengfei, Dodson Matthew, Zhang Donna D, Ghishan Fayez K, Barberán Albert, Kiela Pawel R

机构信息

Department of Environmental Science, University of Arizona, Tucson, Arizona, 85721 USA.

Department of Pediatrics, University of Arizona, Tucson, Arizona, 85724 USA.

出版信息

Front Microbiomes. 2022;1. doi: 10.3389/frmbi.2022.1041188. Epub 2022 Nov 23.

DOI:10.3389/frmbi.2022.1041188
PMID:37779901
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10540274/
Abstract

Inorganic arsenic (iAs) exposure has been associated to various detrimental effects such as development of metabolic syndrome and type 2 diabetes via oxidative stress and induced prolonged activation of the NRF2 transcription factor. Such effects can be aggravated by poor dietary habits. The role of gut microbiota in promoting metabolic changes in response to arsenic has yet to be precisely defined. To address the complexity of the interactions between diet, /NRF2, and gut microbiota, we studied the chronic effects of iAs exposure in wild-type (WT) and mice fed normal (ND) vs. high-fat diet (HFD), on the gut microbial community in the context of hepatic metabolism. We demonstrate that all treatments and interactions influenced bacteria and metabolic profiles, with dietary differences causing a strong overlap of responses between the datasets. By identifying five metabolites of known microbial origin and following their fate across treatments, we provide examples on how gut microbial products can participate in the development of iAs and HFD-induced metabolic disease. Overall, our results underline the importance of the microbial community in driving gut-liver-cross talk during iAs and HFD exposure.

摘要

无机砷(iAs)暴露与多种有害影响有关,例如通过氧化应激以及诱导核因子E2相关因子2(NRF2)转录因子的长期激活而引发代谢综合征和2型糖尿病。不良饮食习惯会加剧这些影响。肠道微生物群在促进砷诱导的代谢变化中的作用尚未得到确切界定。为了解决饮食、NRF2和肠道微生物群之间相互作用的复杂性,我们研究了野生型(WT)和喂食正常饮食(ND)与高脂饮食(HFD)的小鼠在肝脏代谢背景下长期暴露于iAs对肠道微生物群落的影响。我们证明,所有处理和相互作用都会影响细菌和代谢谱,饮食差异导致数据集之间的反应有很大重叠。通过鉴定五种已知微生物来源的代谢物并跟踪它们在不同处理中的变化,我们举例说明了肠道微生物产物如何参与iAs和HFD诱导的代谢疾病的发展。总体而言,我们的结果强调了微生物群落在iAs和HFD暴露期间驱动肠-肝相互作用中的重要性。