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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Comparative effects of fipronil and its metabolites sulfone and desulfinyl on the isolated rat liver mitochondria

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Autor(es):
Tavares, Marco A. [1] ; Palma, Ivo D. F. [1] ; Medeiros, Hyllana C. D. [1] ; Guelfi, Marieli [1] ; Santana, Andreia T. [1] ; Mingatto, Fabio E. [1]
Número total de Autores: 6
Afiliação do(s) autor(es):
[1] UNESP Univ Estadual Paulista, Lab Metab & Toxicol Biochem LaBMeT, BR-17900000 Dracena, SP - Brazil
Número total de Afiliações: 1
Tipo de documento: Artigo Científico
Fonte: ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY; v. 40, n. 1, p. 206-214, JUL 2015.
Citações Web of Science: 11
Resumo

Fipronil is an insecticide extensively used to control pests in crops and animals. There are relates of poisoning due to exposure of fipronil in mammals and the liver has been suggested as potential target. In this study, we evaluated the effects of fipronil and its metabolites sulfone and desulfinyl on the bioenergetics, reactive oxygen species (ROS) production and calcium efflux from mitochondria isolated from rat liver. Fipronil (5-25 mu M) inhibited state-3 respiration in mitochondria energized with glutamate plus malate, substrates of complex I of the respiratory chain and decreased the mitochondrial membrane potential resulting in inhibition of ATP synthesis. Fipronil also caused uncoupling in succinate-energized mitochondria and calcium efflux. The metabolites sulfone and desulfinyl also acted as mitochondrial inhibitors and uncouplers and caused calcium efflux, but with different potencies, being the sulfone the more potent one. These effects of fipronil and its metabolites on mitochondrial bioenergetics and calcium homeostasis may be related to toxic effects of the insecticide in the liver. (C) 2015 Elsevier B.V. All rights reserved. (AU)

Processo FAPESP: 12/15135-6 - Mecanismos de toxicidade do fipronil em mitocôndrias e hepatócitos isolados de ratos
Beneficiário:Fábio Erminio Mingatto
Modalidade de apoio: Auxílio à Pesquisa - Regular