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Experimental & Molecular Medicine ; : 348-356, 2006.
Artigo em Inglês | WPRIM | ID: wpr-53156

RESUMO

Gaucher disease is a glycosphingolipid storage disease caused by deficiency of glucocerebrosidase, resulting in the accumulation of glucosylceramide in lysosomes. The neuronopathic forms of this disease are associated with neuronal loss and neurodegeneration. However, the pathophysiological mechanisms leading to prenatal and neonatal death remain uncharacterized. To investigate brain dysfunction in Gaucher disease, we studied the effects of neurotrophic factors during development in a mouse model of Gaucher disease. The expression of brain-derived neurotrophic factor and nerve growth factor was reduced in the cerebral cortex, brainstem, and cerebellum of Gaucher mice, compared with that in wild-type mice. Extracellular signal-regulated kinase (ERK) 1/2 expression was downregulated in neurons from Gaucher mice and correlated with a decreased number of neurons. These results suggest that a reduction in neurotrophic factors could be involved in neuronal loss in Gaucher disease.


Assuntos
Camundongos , Animais , Transdução de Sinais , Neurônios/metabolismo , Fatores de Crescimento Neural/metabolismo , Modelos Animais , Camundongos Endogâmicos C57BL , Sistema de Sinalização das MAP Quinases/fisiologia , Doença de Gaucher/metabolismo , Regulação para Baixo , Células Cultivadas , Sobrevivência Celular , Encéfalo/metabolismo
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