作者
Friedel Dewulf,Ilias Semmouri,Filip Van Nieuwerburgh,Karel De Schamphelaere,Jana Asselman
摘要
The diverse structures and modes of action (MOAs) of organic pollutants present a challenge in forecasting their environmental toxicity . Aromatic amines , widely used in industrial applications, are of particular interest due to their broad structural variation. Although they have been classified as polar narcotics , due to their narcotic MOA in fish, certain substitution patterns of the aromatically bound amino group exert excess toxicity towards species such as Daphnia magna . The underlying mechanisms bebind this phenomenon remain unclear. Therefore, we investigated how substitution patterns affect the MOA in this aquatic invertebrate . We used transcriptomics to study how three primary aromatic amines (PAAs), namely 4,4’-methylenedianiline (4,4’-MDA), 2,2’-methylenedianiline (2,2’-MDA) and 2,4-toluenediamine (2,4-TDA), affect D. magna . Our experimental design also included two reference compounds, 1-octanol (a non-polar narcotic) and aniline (a polar narcotic in fish, but excess toxicant in D. magna ). Our analysis suggests very distinct biological MOAs for the three PAAs. While the para -substituted 4,4’-MDA treatment showed similar effects as the excess toxicant aniline, its ortho -substituted isomer 2,2’-MDA showed similar effects as the narcotic 1-octanol. Our results indicate a specific influence of substituent positioning in PAAs on their toxicity and MOA towards D. magna . This study illustrates the use of transcriptomics and its associated functional analysis to guide industrial chemical development towards more environmentally safe alternatives. • Substituent positioning of aromatic amines affects their toxicity in D. magna . • The structural isomers 4,4’-MDA and 2,2’-MDA exhibit distinct modes of actions. • 4,4’-MDA mimics excess toxicity effects in D. magna . • 2,2’-MDA exhibits narcotic behaviour in D. magna . • Acute immobilization and gene expression analysis reveal distinct modes of action.