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1.
Environ Sci Pollut Res Int ; 22(23): 19194-202, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26250814

RESUMO

The imazethapyr herbicide (formulation Verosil(®)) was evaluated for phytotoxicity and genotoxicity using a battery of bioassays: (1) the growth inhibition of the green alga Pseudokirchneriella subcapitata, (2) the root growth and germination of the higher plant Lactuca sativa, (3) the genetic damage using the Salmonella/microsome test, and (4) the aneugenic and clastogenic effects on Allium cepa. The Verosil(®) formulation was highly toxic to the non-target green alga (median effective concentration (EC50) = 1.05 ± 0.05 mg active ingredient (a.i.) L(-1)), and concentrations above 10 mg a.i. L(-1) inhibited root elongation in lettuce: relative growth index (RGI) between 0.28 ± 0.01 and 0.66 ± 0.10. No genotoxic effect was observed in S almonella typhimurium at 100 mg a.i. L(-1), either with or without the microsomal fraction. However, significant differences in the frequency of chromosomal aberrations in anaphases and telophases (bridges, chromosome fragments, and vagrants) were observed in A. cepa at concentrations between 0.01 and 1 mg a.i. L(-1) with respect to the control. The frequencies of micronuclei showed significant differences with respect to the control at concentrations between 0.001 and 0.1 mg a.i. L(-1). A very high mitotic index (MI = 93.8 ± 5.8) was observed associated with a high number of cells in the prophase stage at 100 mg a.i. L(-1), indicating cytotoxicity. These results showed that imazethapyr is toxic to the non-target populations in both aquatic and terrestrial ecosystems. This herbicide might also exert clastogenic and aneugenic mitotic damage in higher plants. Therefore, the imazethapyr formulation may constitute an environmental risk to plants.


Assuntos
Herbicidas/toxicidade , Mutagênicos/toxicidade , Ácidos Nicotínicos/toxicidade , Poluentes Químicos da Água/toxicidade , Bioensaio , Clorófitas/efeitos dos fármacos , Clorófitas/crescimento & desenvolvimento , Aberrações Cromossômicas , Dano ao DNA , Lactuca/efeitos dos fármacos , Lactuca/crescimento & desenvolvimento , Testes de Sensibilidade Microbiana , Testes para Micronúcleos , Mitose , Índice Mitótico , Cebolas/efeitos dos fármacos , Raízes de Plantas/efeitos dos fármacos , Raízes de Plantas/crescimento & desenvolvimento , Salmonella typhimurium/efeitos dos fármacos , Salmonella typhimurium/genética
2.
Artigo em Inglês | MEDLINE | ID: mdl-19651240

RESUMO

We analyzed the dietary copper effects in the estuarine crab Neohelice (Chasmagnathus) granulata and its interaction with water salinity. Crabs were maintained at 2 per thousand and 30 per thousand salinity for 5 weeks and they were fed with commercial food supplemented with the green alga Scenedesmus vacuolatus previously exposed to copper. No mortalities were observed, but crabs maintained at 2 per thousand salinity accumulated on average 40% more copper compared to animals maintained at 30 per thousand salinity. At 2 per thousand salinity, superoxide dismutase (SOD) activity and reduced glutathione (GSH) levels were increased at the first and second weeks, respectively, while lipid peroxidation and protein oxidation were evident after 4 weeks of copper exposure. At 30 per thousand salinity, all measured variables increased progressively but were significantly higher only at the end of the assay (5th week), except for protein oxidation that remained unchanged throughout the experiment. The hepatosomatic index (HSI) was significantly decreased in response to copper exposure, but only in crabs acclimated to 2 per thousand. These findings have suggested that dietary copper exposure induces greater metal accumulation and larger oxidative stress responses in crabs maintained at 2 per thousand salinity.


Assuntos
Aclimatação/efeitos dos fármacos , Braquiúros/metabolismo , Cobre/metabolismo , Salinidade , Cloreto de Sódio/farmacologia , Animais , Braquiúros/química , Braquiúros/fisiologia , Relação Dose-Resposta a Droga , Glutationa/análise , Glutationa/metabolismo , Hepatopâncreas/química , Peroxidação de Lipídeos/efeitos dos fármacos , Masculino , Oxirredução , Estresse Oxidativo/efeitos dos fármacos , Proteínas/análise , Padrões de Referência , Rios , Solubilidade , Superóxido Dismutase/metabolismo , Fatores de Tempo
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