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1.
Fish Physiol Biochem ; 36(1): 101-7, 2010 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19082751

RESUMO

The levels of metallothionein (MT), a biomarker of metal exposure, and of Cd and Cu, known as MT inducers, were investigated in Sparus aurata intraperitoneally injected with 500 microg/kg of Cu and Cd for 2 days. MT and metal concentrations (Cd and Cu) were determined in liver, gills and kidney. MT levels were significantly increased in all investigated tissues, with the highest value in liver of Cu as Cd-treated fishes (3.56-fold and 3.3- fold, respectively). Metal concentrations were statistically different between all tissues. Highest metal concentrations were in the liver. The higher metal concentrations and MT induction levels support the main role of MT in metal homeostasis and detoxification.


Assuntos
Estruturas Animais/química , Cádmio/toxicidade , Cobre/toxicidade , Metalotioneína/metabolismo , Metais/metabolismo , Dourada , Animais , Regulação da Expressão Gênica/efeitos dos fármacos , Brânquias/química , Rim/química , Fígado/química , Poluentes Químicos da Água/toxicidade
2.
Fish Physiol Biochem ; 35(2): 293-9, 2009 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-19343524

RESUMO

In the present study biotransformation and detoxification responses to acute exposure to the polycyclic aromatic hydrocarbons benzo[a]pyrene (B[a]P) were investigated in the liver of Sparus aurata (sea bream). Sexually immature gilthead sea bream were treated by intraperitoneal injection of B[a]P (20 mg kg(-1)) for 6, 12, 24, and 48 h. B[a]P accumulation was quantified in sea bream liver by mean of gas phase chromatography (GPC-MS) after the various exposure periods. The following biological responses were measured: (1) ethoxyresorufin-O-deethylase (EROD) activity, as a phase I biotransformation parameter; (2) liver glutathione S-transferase (GST) activity as a phase II conjugation enzyme. DNA damage was assessed over time using the single-cell gel electrophoresis comet assay. B[a]P bioaccumulation in the liver resulted in a biphasic curve with an increasing uptake up to 5.55 +/- 0.67 microg g(-1) dry weight after only 6 h exposure and 4.67 +/- 0.68 microg g(-1) dry weight after 48 h exposure. EROD activity showed a nonsymmetrical bell-shaped kinetic with a maximum at 24 h and lower but significant activities at 12 and 48 h with respect to control animals. Hepatic GST activities were only significant after 48 h exposure. Comet assay showed an increase in liver cells DNA damage with a maximum after 48 h exposure reaching up to 12.17 % DNA in the tail.


Assuntos
Benzo(a)pireno/toxicidade , Citocromo P-450 CYP1A1/metabolismo , Dano ao DNA/efeitos dos fármacos , Glutationa Transferase/metabolismo , Fígado/efeitos dos fármacos , Dourada/fisiologia , Poluentes Químicos da Água/toxicidade , Animais , Benzo(a)pireno/análise , Fígado/química , Fígado/enzimologia
3.
Fish Physiol Biochem ; 34(3): 201-7, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18665457

RESUMO

This research was designed to study Sparus aurata (sea bream) biotransformation and detoxification responses to acute exposure to cadmium (Cd). Sexually immature gilthead sea bream were treated by intraperitoneal injection of Cd chloride (200 microg kg(-1)) for 6, 12, 24 and 48 h. Cd accumulation was quantified in sea bream liver by graphite furnace atomic absorption spectroscopy after the various exposure periods. The following biological responses were measured: (1) ethoxyresorufin-O-deethylase (EROD) activity as phase I biotransformation parameter, (2) liver glutathione-S-transferase (GST) activity as a phase II conjugation enzyme and metallothionein (MT) content as specific response to Cd contamination. Cd bioaccumulation in the liver resulted in an increasing uptake up to 10.3 microg g(-1) wet weight after 48 h of exposure. EROD showed a significant activation only after 6 h exposure and a return to control levels after 12 h. GST revealed significant activation starting from 12 h exposure. MT accumulation in liver showed the same behavior as GST activation.


Assuntos
Cádmio/toxicidade , Citocromo P-450 CYP1A1/metabolismo , Glutationa Transferase/metabolismo , Fígado/efeitos dos fármacos , Metalotioneína/metabolismo , Dourada/metabolismo , Poluentes Químicos da Água/toxicidade , Animais , Fígado/enzimologia , Fígado/metabolismo , Fatores de Tempo
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