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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >TREADMILL TRAINING STIMULATES BRAIN-DERIVED NEUROTROPHIC FACTOR mRNA EXPRESSION IN MOTOR NEURONS OF THE LUMBAR SPINAL CORD IN SPINALLY TRANSECTED RATS
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TREADMILL TRAINING STIMULATES BRAIN-DERIVED NEUROTROPHIC FACTOR mRNA EXPRESSION IN MOTOR NEURONS OF THE LUMBAR SPINAL CORD IN SPINALLY TRANSECTED RATS

机译:跑步训练可刺激脊髓横断大鼠腰椎脊髓神经元中脑源性神经营养因子mRNA的表达

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摘要

Brain-derived neurotrophic factor (BDNF) induces plasticity within the lumbar spinal circuits thereby improving locomotor recovery in spinal cord-injured animals. We examined whether lumbar spinal cord motor neurons and other ventral horn cells of spinally transected (ST) rats were stimulated to produce BDNF mRNA in response to treadmill training. Rats received complete spinal cord transections as neonates (n = 20) and one month later, received four weeks of either a low (100 steps/ training session; n = 10) or high (1000 steps/training session; n = 10) amount of robotic-assisted treadmill training. Using combined non-radioactive in situ hybridization and immunohistochemical techniques, we found BDNF mRNA expression in heat shock protein 27-labeled motor neurons and in non-motor neuron cells was greater after 1000 steps/training session compared to the 100 steps/training session and was similar to BDNF mRNA labeling in untrained Intact rats. In addition, there were significantly more motor neurons that contained BDNF mRNA labeling within processes in the ST rats that received the higher amount of treadmill training. These findings suggested that motor neurons and other ventral horn cells in ST rats synthesized BDNF in response to treadmill training. The findings support a mechanism by which postsynaptic release of BDNF from motor neurons contributed to synaptic plasticity.
机译:脑源性神经营养因子(BDNF)诱导腰脊髓回路内的可塑性,从而改善脊髓损伤动物的运动恢复。我们检查了脊柱横断(ST)大鼠的腰脊髓运动神经元和其他腹角细胞是否被刺激以响应跑步机训练而产生BDNF mRNA。大鼠在新生时(n = 20)接受了完整的脊髓横切术,一个月后,接受了低剂量(100步/训练; n = 10)或高剂量(1000步/训练; n = 10)的四个星期机器人辅助的跑步机训练。使用结合的非放射性原位杂交和免疫组织化学技术,我们发现热休克蛋白27标记的运动神经元和非运动神经元细胞中的BDNF mRNA表达在1000步/训练后比100步/训练和更高。与未经训练的完整大鼠的BDNF mRNA标记相似​​。此外,在接受大量跑步机训练的ST大鼠的过程中,含有BDNF mRNA标记的运动神经元明显增多。这些发现提示ST大鼠的运动神经元和其他腹角细胞响应跑步训练而合成了BDNF。这些发现支持了运动神经元突触后释放BDNF有助于突触可塑性的机制。

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