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Toxicol Lett ; 151(1): 69-78, 2004 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-15177642

RESUMO

The expression of MDR1b coding mRNA is increased in alveolar type II cells from juvenile rat lung in culture. Hydrogen peroxide and paraquat-induced further upregulation supporting that oxidative stress mediated mechanisms are involved in the regulation of MDR1b in rat lung. The expression rates of mRNA for catalase, Cu/Zn-superoxide dismutase (Cu/Zn-SOD) and Mn-superoxide dismutase (Mn-SOD) remains constant during culture and were not modulated by hydrogen peroxide or paraquat. Thus, antioxidative enzymes in primary A II cells from rat lung are not regulated by reactive oxygen species dependent mechanisms. Primary A II cells were substantially more sensitive towards paraquat-induced cytotoxicity and lipid peroxidation than the permanent human lung tumor cell lines H322 and H358. A 100 microM hydrogen peroxide for 2h induces substantial DNA damage which is not paralleled by an increased rate of lipid peroxidation. The expression rate of mRNA coding for catalase and Mn-SOD was not changed and almost the same is true for the activity of catalase and Cu/Zn-SOD. Only 50 microM paraquat induced a significant decrease in catalase activity and an increase in Cu/Zn-SOD activity.


Assuntos
Subfamília B de Transportador de Cassetes de Ligação de ATP/metabolismo , Peróxido de Hidrogênio/farmacologia , Neoplasias Pulmonares/tratamento farmacológico , Neoplasias Pulmonares/metabolismo , Paraquat/farmacologia , Alvéolos Pulmonares/efeitos dos fármacos , Alvéolos Pulmonares/metabolismo , Subfamília B de Transportador de Cassetes de Ligação de ATP/genética , Animais , Catalase/metabolismo , Linhagem Celular Tumoral , Humanos , Peróxido de Hidrogênio/toxicidade , Neoplasias Pulmonares/patologia , Masculino , Malondialdeído/metabolismo , Microscopia Eletrônica , Estresse Oxidativo/fisiologia , Paraquat/toxicidade , Alvéolos Pulmonares/patologia , RNA/genética , Ratos , Ratos Wistar , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Superóxido Dismutase/metabolismo , Membro 4 da Subfamília B de Transportadores de Cassetes de Ligação de ATP
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