Toxicity assessment of the herbicide metolachlor comparative effects on bacterial and mitochondrial model systems

• Autor(a) principal: Pereira, Susana P.
• Data de Publicação: 2009
• Outros Autores: Fernandes, Maria A. S., Martins, João D., Santos, Maria S., Moreno, António J. M., Vicente, Joaquim A. F., Videira, Romeu A., Jurado, Amália S.
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
• Texto Completo: http://hdl.handle.net/10316/47551; https://doi.org/10.1016/j.tiv.2009.06.032
• topic: Acetamides; Animals; Dose-Response Relationship, Drug; Energy Metabolism; Geobacillus stearothermophilus; Herbicides; Male; Membrane Potential, Mitochondrial; Mitochondria, Liver; Oxygen Consumption; Rats; Rats, Wistar; Acetamides; Animals; Dose-Response Relationship, Drug; Energy Metabolism; Geobacillus stearothermophilus; Herbicides; Male; Membrane Potential, Mitochondrial; Mitochondria, Liver; Oxygen Consumption; Rats; Rats, Wistar

Metolachlor is one of the most intensively used chloroacetamide herbicides. However, its effects on the environment and on non-target animals and humans as well as its interference at a cell/molecular level have not yet been fully elucidated. The aim of this study was: firstly, to evaluate the potential toxicity of metolachlor at a cell/subcellular level by using two in vitro biological model systems (a strain of Bacillus stearothermophilus and rat liver mitochondria); secondly, to evaluate the relative sensibility of these models to xenobiotics to reinforce their suitability for pollutant toxicity assessment. Our results show that metolachlor inhibits growth and impairs the respiratory activity of B.stearothermophilus at concentrations two to three orders of magnitude higher than those at which bacterial cells are affected by other pesticides. Also at concentrations significantly higher than those of other pesticides, metolachlor depressed the respiratory control ratio, membrane potential and respiration of rat liver mitochondria when malate/glutamate or succinate were used as respiratory substrates. Moreover, metolachlor impaired the respiratory activity of rat liver mitochondria in the same concentration range at which it inhibited bacterial respiratory system (0.4-5.0 micromol/mg of protein). In conclusion, the high concentration range at which metolachlor induces toxicity in vitro suggests that this compound is safer than other pesticides previously studied in our laboratory, using the same model systems. The good parallelism between metolachlor effects on both models and the toxicity data described in the literature, together with results obtained in our laboratory with other compounds, indicate the suitability of these systems to assess toxicity in vitro.