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Sci Rep ; 10(1): 1936, 2020 02 11.
Artículo en Inglés | MEDLINE | ID: mdl-32041968

RESUMEN

Development of pharmacotherapies that promote remyelination is a high priority for multiple sclerosis (MS), due to their potential for neuroprotection and restoration of function through repair of demyelinated lesions. A novel preparation of clean-surfaced, faceted gold nanocrystals demonstrated robust remyelinating activity in response to demyelinating agents in both chronic cuprizone and acute lysolecithin rodent animal models. Furthermore, oral delivery of gold nanocrystals improved motor functions of cuprizone-treated mice in both open field and kinematic gait studies. Gold nanocrystal treatment of oligodendrocyte precursor cells in culture resulted in oligodendrocyte maturation and expression of myelin differentiation markers. Additional in vitro data demonstrated that these gold nanocrystals act via a novel energy metabolism pathway involving the enhancement of key indicators of aerobic glycolysis. In response to gold nanocrystals, co-cultured central nervous system cells exhibited elevated levels of the redox coenzyme nicotine adenine dinucleotide (NAD+), elevated total intracellular ATP levels, and elevated extracellular lactate levels, along with upregulation of myelin-synthesis related genes, collectively resulting in functional myelin generation. Based on these preclinical studies, clean-surfaced, faceted gold nanocrystals represent a novel remyelinating therapeutic for multiple sclerosis.


Asunto(s)
Nanopartículas del Metal/uso terapéutico , Esclerosis Múltiple/tratamiento farmacológico , Células Precursoras de Oligodendrocitos/efectos de los fármacos , Remielinización/efectos de los fármacos , Animales , Apoptosis/efectos de los fármacos , Fenómenos Biomecánicos/efectos de los fármacos , Movimiento Celular/efectos de los fármacos , Cuprizona , Modelos Animales de Enfermedad , Perfilación de la Expresión Génica , Oro , Nanopartículas del Metal/administración & dosificación , Ratones , Movimiento/efectos de los fármacos , Esclerosis Múltiple/inducido químicamente , Esclerosis Múltiple/patología , Células Precursoras de Oligodendrocitos/patología , Transducción de Señal/efectos de los fármacos , Transducción de Señal/genética
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