Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Chem Res Toxicol ; 17(12): 1551-61, 2004 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-15606129

RESUMO

Adverse drug reactions are a major clinical problem. Drug-induced hepatotoxicity constitutes a large percentage of these reactions. A thorough understanding of the genetic events, specifically, the early "decision-making" processes underlying biological changes caused by drugs and metabolites, is required. To assist in the understanding of these events, we have employed the model hepatotoxin, paracetamol (APAP), and GeneChip technology to investigate global genetic events seen after nontoxic and toxic doses in the mouse. Mice were dosed [vehicle, nontoxic APAP (1 mmol/kg), and toxic APAP (3.5 mmol/kg)], and individual hepatic RNA samples were hybridized to separate chips to determine interanimal variation. Statistical analysis detected 175 CD-1 mouse genes that were significantly regulated (P < 4.1 x 10(-6)), and nonsignificant genes were discarded. For clarity, the significantly regulated genes were then binned into categories according to their major function-antioxidant, glutathione, metabolism, transcription, immune, and apoptosis. There was no hepatic stress observed after dosing 1 mmol/kg APAP, when measured by serum alanine aminotransferase levels. Hepatic toxicity was observed at both 4 and 24 h after a 3.5 mmol/kg dose of APAP. Time course expression profiles for selected genes have been created. These results demonstrate that most active gene expression occurs around 4 h after a toxic dose of APAP. Down-regulation of these genes is observed over 24 h, coinciding with the development of overt toxicity. These data provide a deeper understanding of the in vivo time course of physiological responses of the liver to chemical stress and provide a logical step forward for the investigation of new chemical entities demonstrated positive in chemically reactive metabolite screens. The complete data set can be viewed at http://www.ebi.ac.uk/arrayexpress/. The accession number is E-MEXP-82.


Assuntos
Acetaminofen/toxicidade , Expressão Gênica/efeitos dos fármacos , Fígado/efeitos dos fármacos , Acetaminofen/farmacologia , Animais , Dipeptídeos/genética , Regulação para Baixo , Perfilação da Expressão Gênica , Proteínas de Choque Térmico/genética , Fígado/enzimologia , Masculino , Camundongos , Fatores de Tempo , Regulação para Cima
2.
J Parasitol ; 82(2): 338-9, 1996 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-8604111

RESUMO

Neospora caninum tissue cysts were found in sections of the brain from a full-term stillborn deer of Eld (Cervus eldi siamensis) from a zoo in France. There was N. caninum-associated nonsuppurative encephalitis and the diagnosis was confirmed in immunohistochemical staining with antibodies specific to N. caninum.


Assuntos
Encéfalo/parasitologia , Coccidiose/veterinária , Cervos/parasitologia , Morte Fetal/veterinária , Neospora/isolamento & purificação , Animais , Encéfalo/embriologia , Encéfalo/patologia , Coccidiose/diagnóstico , Coccidiose/parasitologia , Encefalite/embriologia , Encefalite/parasitologia , Encefalite/veterinária , Feminino , Morte Fetal/parasitologia , Masculino , Gravidez , Complicações Parasitárias na Gravidez/parasitologia , Complicações Parasitárias na Gravidez/veterinária
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...