首页> 外文期刊>Neuroscience & Medicine >Depletion of Glial Cell Line-Derived Neurotrophic Factor by Disuse Muscle Atrophy Exacerbates the Degeneration of Alpha Motor Neurons in Caudal Regions Remote from the Spinal Cord Injury
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Depletion of Glial Cell Line-Derived Neurotrophic Factor by Disuse Muscle Atrophy Exacerbates the Degeneration of Alpha Motor Neurons in Caudal Regions Remote from the Spinal Cord Injury

机译:废用肌肉萎缩引起的胶质细胞源性神经营养因子耗竭加剧了远离脊髓损伤的尾区的α运动神经元的变性。

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We have been previously reported that disuse muscle atrophy exacerbates both motor neuron (MN) degeneration in caudal regions remote from a spinal cord injury, and decrease in glial cell line-derived neurotrophic factor (GDNF) protein level in paralyzed muscle. In this study we found that disuse muscle atrophy exacerbated the decrease in GDNF protein level in the L4/5 spinal cord, which was not immunopositive for GDNF. Our results were consistent with the fact that in the lumbar spinal cord of rats with mid-thoracic contusion, GDNF expression was not detected, while expression of GDNF receptors (GFRα1 and RET) was. Our study showed that administration of exogenous recombinant GDNF into the atrophic muscle partially rescued α-MN degeneration in the L4/5 spinal cord. These results suggest that the depletion of GDNF protein by muscle atrophy exacerbates α-MN degeneration in caudal regions remote from the injury.
机译:以前我们已经报道过,废用的肌肉萎缩加剧了远离脊髓损伤的尾区的运动神经元(MN)变性,并使神经胶质细胞系衍生的神经营养因子(GDNF)蛋白水平降低。在这项研究中,我们发现废用的肌肉萎缩加剧了L4 / 5脊髓中GDNF蛋白水平的下降,而这对于GDNF并不是免疫阳性的。我们的结果与以下事实相吻合:在胸中部挫伤大鼠的腰脊髓中未检测到GDNF表达,而在GDNF受体(GFRα1和RET)中表达。我们的研究表明,向萎缩性肌肉中施用外源重组GDNF可部分挽救L4 / 5脊髓中的α-MN变性。这些结果表明,肌肉萎缩对GDNF蛋白的消耗加剧了远离损伤的尾区的α-MN变性。

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