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Dent Mater J ; 24(3): 304-10, 2005 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-16279718

RESUMO

The purpose of this study was to clarify the cytotoxicity of Ni2+ ions against murine peritoneal exudate cells (PEC) (macrophages). First, we examined the cell viability of PEC with and without lipopolysaccharide (LPS) stimulation in culture media containing Ni2+ ions up to 1000 micromol/L. Results showed that the cytotoxicity of Ni2+ ions against PEC was dose-dependent and accelerated by LPS stimulation, especially in media with Ni2+ ions exceeding 100 micromol/L. Second, we measured the production of nitric oxide (NO) from PEC and found that LPS caused the PEC to produce abundant NO. However, high dose of Ni2+ ions at concentration more than 200 micromol/L hindered and inhibited NO production. These results pointed out that the cytotoxicity of Ni2+ ions against macrophages depended on both the Ni2+ ion concentration and the presence of bacteria with LPS. Further, NO--a killer of bacteria--was lost when LPS-stimulated macrophages were exposed to high dose of Ni2+ ions.


Assuntos
Sequestradores de Radicais Livres/metabolismo , Lipopolissacarídeos/toxicidade , Macrófagos Peritoneais/efeitos dos fármacos , Níquel/toxicidade , Óxido Nítrico/biossíntese , Actinas/análise , Animais , Sobrevivência Celular/efeitos dos fármacos , Células Cultivadas , Relação Dose-Resposta a Droga , Interleucina-1/análise , Interleucina-6/análise , Lipopolissacarídeos/administração & dosagem , Camundongos , Níquel/administração & dosagem , Óxido Nítrico/análise , Óxido Nítrico Sintase/análise , Óxido Nítrico Sintase/efeitos dos fármacos , RNA Mensageiro/análise , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Fator de Necrose Tumoral alfa/análise , Fator de Necrose Tumoral alfa/efeitos dos fármacos
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