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Artículo en Inglés | WPRIM | ID: wpr-285231

RESUMEN

Evidence suggested that glycogen synthase kinase-3β (GSK-3β) is involved in Nogo-66 inhibiting axonal regeneration in vitro, but its effect in vivo was poorly understood. We showed that stereotactic injection of shRNA GSK-3β-adeno associated virus (GSK-3β-AAV) diminished syringomyelia and promoted axonal regeneration after spinal cord injury (SCI), using stereotactic injection of shRNA GSK-3β-AAV (tested with Western blotting and RT-PCR) into the sensorimotor cortex of rats with SCI and by the detection of biotin dextran amine (BDA)-labeled axonal regeneration. We also determined the right position to inject into the sensorimotor cortex. Our findings consolidate the hypothesis that downregulation of GSK-3β promotes axonal regeneration after SCI.


Asunto(s)
Animales , Humanos , Ratas , Axones , Metabolismo , Dependovirus , Genética , Glucógeno Sintasa Quinasa 3 beta , Genética , Metabolismo , Regeneración Nerviosa , Genética , ARN Interferente Pequeño , Genética , Corteza Sensoriomotora , Patología , Traumatismos de la Médula Espinal , Genética , Patología , Terapéutica , Siringomielia , Genética , Patología , Terapéutica
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