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Growth factor stimulated functional improvement following cortical ischemia.

机译:生长因子刺激皮质缺血后的功能改善。

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摘要

The current study investigates the use of a growth factor treatment (epidermal growth factor (EGF) followed by erythropoietin (EPO)) to treat motor impairment following cortical ischemia in the rat. Treatment with EGF+EPO following ischemic damage of the primary motor cortex resulted in are-growth of tissue within the lesion site concomitant with functional motor improvements of the forepaw. Investigation of the functional improvement resulted in the finding that EGF+EPO treated rats engaged in behavioural compensation when completing a skilled forepaw task; whereas control treated rats did not. In order to understand the role of the new tissue in functional improvements intracortical microstimulation and aspiration of the new tissue was performed. Direct stimulation of the new tissue did not result in observable functional output, indicating that the new tissue is not directly responsible for functional improvement. Tissue adjacent to the lesion site, in EGF+EPO treated rats, did show significant reorganization compared to control treated rats. Thus, EGF+EPO may playa role in functional improvement by increasing cortical plasticity. Aspiration of the new tissue following functional improvement led to a delayed reinstatement of the functional deficit, alongside a shrinking of cortical forepaw representation. These data confirm that the new tissue is not directly responsible for functional improvements following cortical ischemia. Finally, EGF+EPO treatment appears to improve motor learning and increase cortical reorganization in the absence of cortical injury. Taken together, these data show that EGF+EPO may facilitate motor learning and cortical plasticity, both of which are imperative for functional recovery following injury of the motor cortex.
机译:本研究调查了使用生长因子治疗(表皮生长因子(EGF),然后促红细胞生成素(EPO))来治疗大鼠皮质缺血后的运动障碍。在原发性运动皮层缺血性损伤后用EGF + EPO进行治疗会导致病变部位组织的生长,并伴随前臂的功能性运动改善。对功能改善的研究导致发现,在完成熟练的前爪任务时,用EGF + EPO处理的大鼠会进行行为补偿。而对照组则没有。为了了解新组织在功能改善中的作用,进行了新组织的皮层内微刺激和抽吸。对新组织的直接刺激并未导致可观察到的功能输出,表明新组织对功能改善没有直接作用。与对照治疗的大鼠相比,EGF + EPO治疗的大鼠中病变部位附近的组织确实显示出明显的重组。因此,EGF + EPO可能通过增加皮质可塑性而在功能改善中发挥作用。功能改善后对新组织的抽吸导致功能缺损的恢复延迟,同时前额皮层代表性缩小。这些数据证实,新组织不直接负责皮质缺血后的功能改善。最后,在没有皮层损伤的情况下,EGF + EPO治疗似乎可以改善运动学习并增加皮层重组。综上所述,这些数据表明,EGF + EPO可能促进运动学习和皮质可塑性,这对于运动皮层损伤后的功能恢复都是必不可少的。

著录项

  • 作者

    Chalmers, Trudi E.;

  • 作者单位

    University of Calgary (Canada).;

  • 授予单位 University of Calgary (Canada).;
  • 学科 Biology Neuroscience.;Psychology Behavioral.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 171 p.
  • 总页数 171
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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