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Review
. 2015;56(2):218-27.
doi: 10.1093/ilar/ilv018.

Xenobiotics: Interaction with the Intestinal Microflora

Affiliations
Review

Xenobiotics: Interaction with the Intestinal Microflora

Kun Lu et al. ILAR J. 2015.

Abstract

The human body is host to 100 trillion gut microbes, approximately 10-times more than all human cells. It is estimated that the approximately 500-1000 species residing in the human gut encode 150-fold more unique genes than the human genome. The gut microbiota has important functions in metabolic processing, such as energy production, immune cell development, food digestion, and epithelial homeostasis. It has been increasingly recognized that a dysregulated gut microbiome contributes in a significant way to a variety of diseases, including diabetes, obesity, cardiovascular diseases, allergies, and inflammatory bowel disease. In particular, accumulating evidence indicates that functional interactions between the gut microbiome and xenobiotics play a role in mediating chemical toxicity and causing or exacerbating human disease. This review summarizes emerging evidence that illustrates how xenobiotics can affect the gut microbiome structure, create functional changes to the gut microbiome, and become biotransformed by the gut microbiome.

Keywords: gut microbiome; interaction; xenobiotics.

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References

    1. Alava P, Tack F, Laing GD, van de Wiele T. 2013. Arsenic undergoes significant speciation changes upon incubation of contaminated rice with human colon micro biota. J Hazard Mater 262:1237–1244. - PubMed
    1. Alkhouri N, Cikach F, Eng K, Moses J, Patel N, Yan C, Hanouneh I, Grove D, Lopez R, Dweik R. 2014. Analysis of breath volatile organic compounds as a noninvasive tool to diagnose nonalcoholic fatty liver disease in children. Eur J Gastroenterol Hepatol 26:82–87. - PubMed
    1. Altieri L, Neri C, Sacco R, Curatolo P, Benvenuto A, Muratori F, Santocchi E, Bravaccio C, Lenti C, Saccani M, Rigardetto R, Gandione M, Urbani A, Persico AM. 2011. Urinary p-cresol is elevated in small children with severe autism spectrum disorder. Biomarkers 16:252–260. - PubMed
    1. Baker NA, Shoemaker R, English V, Larian N, Sunkara M, Morris AJ, Walker M, Yiannikouris F, Cassis LA. 2015. Effects of adipocyte aryl hydrocarbon receptor deficiency on PCB-induced disruption of glucose homeostasis in lean and obese mice. Environ Health Perspect [Epub ahead of print]. - PMC - PubMed
    1. Barbosa SM, Farhat SC, Martins LC, Pereira LA, Saldiva PH, Zanobetti A, Braga AL. 2015. Air pollution and children's health: sickle cell disease. Cad Saude Publica 31:265–275. - PubMed

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