首页> 中文期刊> 《中华创伤杂志(英文版)》 >Protective effect of liposome-mediated glial cell line-derived neurotrophic factor gene transfer in vivo on motoneurons following spinal cord injury in rats

Protective effect of liposome-mediated glial cell line-derived neurotrophic factor gene transfer in vivo on motoneurons following spinal cord injury in rats

         

摘要

Objective:To investigate the effect of liposomemediated glial cell line-derived neurotrophic factor (GDNF) gene transfer in vivo on spinal cord motoneurons after spinal cord injury (SCI) in adult rats.Methods: Sixty male Sprague-Dawley rats were divided equally into two groups: GDNF group and control group. The SCI model was established according to the method of Nystrom, and then the DC-Chol liposomes and recombinant plasmid pEGFP-GDNF cDNA complexes were injected into the injured spinal cord. The expression of GDNF cDNA 1 week after injection was detected by RTPCR and fluorescence microscope. We observed the remaining motoneurons in the anterior horn and the changes of cholinesterase (CHE) and acid phosphatase (ACP) activity using Nissl and enzyme histochemistry staining. The locomotion function of hind limbs of rats was evaluated using inclined plane test and BBB locomotor scale.Results: RT-PCR and fluorescence observation confirmed the presence of expression of GDNF cDNA 1week and 4 weeks after injection. At 1, 2, 4 weeks after SCI, the number of motoneurons in the anterior horn in GDNF group (20.4±3.2, 21.7±3.6, 22.5±3.4) was more than that in control group ( 16.8±2.8, 17.3 ± 2.7,18.2±3.2, P<0.05). At 1, 2 weeks after SCI, the mean gray of the CHE-stained spinal motoneurons in GDNF group (74.2± 25.8, 98.7± 31.6 was less than that in control group (98.5 ±32.2, 134.6 ±45.2, P<0.01), and the mean gray of ACP in GDNF group (84.5±32.6, 79.5±28.4) was more than that in control group (61.2±24.9,52.6±19.9, P<0.01). The locomotion functional scales in GDNF group were higher than that in control group within 1 to 4 weeks after SCI (P<0.05).Conclusions: GDNF gene transfer in vivo can protect motoneurons from death and degeneration induced by incompleted spinal cord injury as well as enhance locomotion functional restoration of hind limbs. These results suggest that liposome-mediated delivery of GDNF cDNA might be a practical method for treating traumatic spinal cord injury.

著录项

  • 来源
    《中华创伤杂志(英文版)》 |2004年第5期|275-279|共5页
  • 作者

    鲁凯伍; 陈哲宇; 侯铁胜;

  • 作者单位

    Department of Orthopedic and Spine Surgery, Nanfang Hospital, First Military Medical University, Guangzhou 510515,China;

    Department of Orthopedic and Spine Surgery, Nanfang Hospital, First Military Medical University, Guangzhou 510515,China;

    Department of Orthopedic and Spine Surgery, Nanfang Hospital, First Military Medical University, Guangzhou 510515,China;

  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类
  • 关键词

    Spinal cord injury; Motor neurons; Liposome; Gene therapy;

    机译:脊髓损伤;运动神经元;脂质体;基因治疗;
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号