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Aniline Is Rapidly Converted Into Paracetamol Impairing Male Reproductive Development.

Authors :
Holm, Jacob Bak
Chalmey, Clementine
Modick, Hendrik
Jensen, Lars Skovgaard
Dierkes, Georg
Weiss, Tobias
Jensen, Benjamin Anderschou Holbech
Nørregård, Mette Marie
Borkowski, Kamil
Styrishave, Bjarne
Koch, Holger Martin
Mazaud-Guittot, Severine
Jegou, Bernard
Kristiansen, Karsten
Kristensen, David Møbjerg
Source :
Toxicological Sciences. Nov2015, Vol. 148 Issue 1, p288-298. 11p. 4 Graphs.
Publication Year :
2015

Abstract

Industrial use of aniline is increasing worldwide with production estimated to surpass 5.6 million metric tons in 2016. Exposure to aniline occurs via air, diet, and water augmenting the risk of exposing a large number of individuals. Early observations suggest that aniline is metabolized to paracetamol/acetaminophen, likely explaining the omnipresence of low concentrations of paracetamol in European populations. This is of concern as recent studies implicate paracetamol as a disrupter of reproduction. Here, we show through steroidogenic profiling that exposure to aniline led to increased levels of the D4 steroids, suggesting that the activity of CYP21 was decreased. By contrast, paracetamol decreased levels of androgens likely through inhibition of CYP17A1 activity.We confirmthat aniline in vivo is rapidly converted to paracetamol by the liver. Intrauterine exposure to aniline and paracetamol in environmental and pharmaceutical relevant doses resulted in shortening of the anogenital distance inmice, a sensitivemarker of fetal androgen levels that in humans is associated with reproductive malformations and later life reproductive disorders. In conclusion, our results provide evidence for a scenario where aniline, through its conversion into antiandrogenic paracetamol, impairsmale reproductive development. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10966080
Volume :
148
Issue :
1
Database :
Academic Search Index
Journal :
Toxicological Sciences
Publication Type :
Academic Journal
Accession number :
110587755
Full Text :
https://doi.org/10.1093/toxsci/kfv179