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Exercise alters glial cell line-derived neurotrophic factor (GDNF) protein content in the spinal cord.

机译:运动会改变脊髓中神经胶质细胞源性神经营养因子(GDNF)蛋白的含量。

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摘要

Neurotrophic factors may play a role in exercise-induced neuroprotective effects; however, it is not known if exercise mediates changes in glial cell line-derived neurotrophic factor (GDNF) protein levels in the spinal cord. The aim of the studies described herein was to determine if exercise alters GDNF protein expression in the lumbar spinal cord of healthy and diseased animals. The lumbar spinal cord was analyzed from adult rats aged 6-, 12-, 18- and 24-months, and from transgenic amyotrophic lateral sclerosis (ALS) mice and wild-type mice aged 3 months. Animals had undergone either forced wheel running, voluntary wheel running or swimming for either 2- or 4-weeks or 6 months in duration. GDNF protein was quantified via enzyme-linked immunosorbent assay and Western blot. Immunohistochemical analysis localized GDNF in choline acetyltransferase (ChAT)-positive motor neurons and cell body areas were measured. Results indicate that short-term exercise (2 weeks) increases GDNF protein content in the rodent lumbar spinal cord. Chronic exercise (4 weeks to 6 months) has no effect on GDNF protein content in the rodent lumbar spinal cord. All exercise protocols increased the size of ChAT-positive motor neuron cell body areas of healthy, non-diseased animals. Treatment with neutralizing antibodies for GDNF in the transgenic ALS animals blocked the beneficial effects of exercise on motor neurons. These results suggest that short-term exercise elicits an increase in neurotrophic factors via an activity-dependent relationship that occurs with GDNF protein expression in spinal cord. Understanding how neurotrophic factors are regulated by physical activity is crucial for maintaining a healthy motor nervous system and for developing therapies for individuals with compromised motor nervous systems, e.g. due to aging or disease.
机译:神经营养因子可能在运动引起的神经保护作用中起作用;然而,尚不清楚运动是否介导脊髓中神经胶质细胞源性神经营养因子(GDNF)蛋白水平的改变。本文所述研究的目的是确定运动是否改变健康和患病动物的腰脊髓中GDNF蛋白的表达。分别从6、12、18、24个月大的成年大鼠以及3个月大的转基因肌萎缩性侧索硬化症(ALS)小鼠和野生型小鼠中分析了腰脊髓。动物经历了强制轮转,自愿轮转或游泳持续了2或4周或6个月的时间。 GDNF蛋白通过酶联免疫吸附测定和Western印迹进行定量。免疫组织化学分析测定了GDNF在胆碱乙酰转移酶(ChAT)阳性运动神经元和细胞体区域的定位。结果表明,短期运动(2周)会增加啮齿动物腰脊髓中GDNF的蛋白质含量。长期运动(4周至6个月)对啮齿动物腰脊髓中GDNF蛋白含量没有影响。所有锻炼方案都会增加健康的,未患病动物的ChAT阳性运动神经元细胞体区域的大小。在转基因ALS动物中用针对GDNF的中和抗体进行治疗,阻断了运动对运动神经元的有益作用。这些结果表明,短期运动通过与脊髓中GDNF蛋白表达有关的活动依赖性关系引起神经营养因子的增加。了解体育锻炼如何调节神经营养因子对于维持健康的运动神经系统和开发针对运动神经系统受损的个体的疗法至关重要。由于衰老或疾病。

著录项

  • 作者

    McCullough, Monica J.;

  • 作者单位

    Western Michigan University.;

  • 授予单位 Western Michigan University.;
  • 学科 Biology Neuroscience.;Biology Physiology.;Health Sciences Recreation.;Health Sciences Aging.
  • 学位 Ph.D.
  • 年度 2013
  • 页码 205 p.
  • 总页数 205
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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