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.

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。

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