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1.
Biomed Res Int ; 2015: 381264, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26339609

RESUMO

The benzonitrile herbicides bromoxynil, chloroxynil, dichlobenil, and ioxynil have been used actively worldwide to control weeds in agriculture since 1970s. Even though dichlobenil is prohibited in EU since 2008, studies addressing the fate of benzonitrile herbicides in the environment show that some metabolites of these herbicides are very persistent. We tested the cytotoxic effects of benzonitrile herbicides and their microbial metabolites using two human cell lines, Hep G2 and HEK293T, representing liver and kidneys as potential target organs in humans. The cell viability and proliferation were determined by MTT test and RTCA DP Analyzer system, respectively. The latter allows real-time monitoring of the effect of added substances. As the cytotoxic compounds could compromise cell membrane integrity, the lactate dehydrogenase test was performed as well. We observed high toxic effects of bromoxynil, chloroxynil, and ioxynil on both tested cell lines. In contrast, we determined only low inhibition of cell growth in presence of dichlobenil and microbial metabolites originating from the tested herbicides.


Assuntos
Proliferação de Células/efeitos dos fármacos , Sobrevivência Celular/efeitos dos fármacos , Herbicidas/toxicidade , Nitrilas/toxicidade , Membrana Celular/efeitos dos fármacos , Células HEK293 , Células Hep G2 , Humanos , Rim/efeitos dos fármacos , Fígado/efeitos dos fármacos
2.
J Ind Microbiol Biotechnol ; 39(12): 1811-9, 2012 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-22922990

RESUMO

The aim of this work was to determine the ability of rhodococci to transform 3,5-dichloro-4-hydroxybenzonitrile (chloroxynil), 3,5-dibromo-4-hydroxybenzonitrile (bromoxynil), 3,5-diiodo-4-hydroxybenzonitrile (ioxynil) and 2,6-dichlorobenzonitrile (dichlobenil); to identify the products and determine their acute toxicities. Rhodococcus erythropolis A4 and Rhodococcus rhodochrous PA-34 converted benzonitrile herbicides into amides, but only the former strain was able to hydrolyze 2,6-dichlorobenzamide into 2,6-dichlorobenzoic acid, and produced also more of the carboxylic acids from the other herbicides compared to strain PA-34. Transformation of nitriles into amides decreased acute toxicities for chloroxynil and dichlobenil, but increased them for bromoxynil and ioxynil. The amides inhibited root growth in Lactuca sativa less than the nitriles but more than the acids. The conversion of the nitrile group may be the first step in the mineralization of benzonitrile herbicides but cannot be itself considered to be a detoxification.


Assuntos
Amidoidrolases/metabolismo , Herbicidas/metabolismo , Hidroliases/metabolismo , Nitrilas/metabolismo , Rhodococcus/metabolismo , Amidas/metabolismo , Amidas/toxicidade , Benzamidas/metabolismo , Biotransformação , Herbicidas/química , Hidrólise , Iodobenzenos/metabolismo , Lactuca/efeitos dos fármacos , Lactuca/crescimento & desenvolvimento , Nitrilas/química , Nitrilas/toxicidade , Raízes de Plantas/efeitos dos fármacos , Raízes de Plantas/crescimento & desenvolvimento , Raízes de Plantas/metabolismo
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