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肠道微生物群限制了慢性口服暴露引起的重金属负担。

Gut microbiota limits heavy metals burden caused by chronic oral exposure.

机构信息

Bactéries Lactiques & Immunité des Muqueuses, Centre d'Infection et d'Immunité de Lille, Institut Pasteur de Lille, Inserm U 1019, CNRS UMR 8204 Université Lille Nord de France, 1 rue du Pr Calmette, BP 245, F-59019 Lille, France.

出版信息

Toxicol Lett. 2013 Oct 24;222(2):132-8. doi: 10.1016/j.toxlet.2013.07.021. Epub 2013 Aug 2.

Abstract

Environmental exposure to pollutants such as heavy metal(s) is responsible for various altered physiological functions which are detrimental for health. The gut microbiota is critical for intestinal homeostasis but its role on xenobiotic handling is not fully understood, especially when continuous sub-chronic exposure is addressed. We first confirmed the essential role of the intestinal microbiome to limit heavy metal body burden by using germ-free mice following 6-weeks oral exposure. Significant increases of cadmium and lead absorption and dissemination in blood and target organs were measured in germ-free mice when compared with conventional specific pathogen free (SPF) mice. Besides the "barrier" function of the luminal microbiota, this may involve specific host-genes such as metallothioneins, which are differentially expressed in the gastrointestinal tract of each group of mice. Considering genes relevant for divalent metal transporters and oxidative pathways, significant differences in basal gene expression were measured between control and germ-free mice. Moreover, the magnitude of induction of these genes upon stimulation by heavy metals varied greatly depending on the dose and type of metal as well as the microbial status of the animal. Collectively, these data illustrate the complex host-microbes interplay occurring with environmental pollutants inside the gut.

摘要

环境污染物(如重金属)暴露会导致各种生理功能改变,对健康有害。肠道微生物群对肠道内稳态至关重要,但人们对其在外来化合物处理中的作用还不完全了解,特别是当涉及到持续的亚慢性暴露时。我们首先通过对无菌小鼠进行 6 周的口服暴露,证实了肠道微生物组在限制重金属体内负荷方面的重要作用。与传统的特定病原体无菌 (SPF) 小鼠相比,无菌小鼠的镉和铅吸收和在血液和靶器官中的传播显著增加。除了腔微生物的“屏障”功能外,这可能还涉及到特定的宿主基因,如金属硫蛋白,它们在每组小鼠的胃肠道中表达不同。考虑到与二价金属转运体和氧化途径相关的基因,在无菌和对照组小鼠之间测量到基础基因表达存在显著差异。此外,这些基因在重金属刺激下的诱导程度因金属的剂量和类型以及动物的微生物状态而异。总的来说,这些数据说明了肠道内环境污染物存在着复杂的宿主-微生物相互作用。

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