Development of artificial tubes to be used for repairing a large peripheral nerve gap

开发用于修复大周围神经间隙的人工管

基本信息

  • 批准号:
    11559010
  • 负责人:
  • 金额:
    $ 4.61万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (B).
  • 财政年份:
    1999
  • 资助国家:
    日本
  • 起止时间:
    1999 至 2000
  • 项目状态:
    已结题

项目摘要

First of all, we have developed the method by which the basal laminae can be restored after cellular components had been removed from the skeletal muscle fiber : the fresh muscle tissue was treated by detergent(3% sodium dodecyl sulfate, 2 days 37 ℃). Such detergent-treated muscle tissues were grafted into the rat sciatic nerve. Many regenerating fibers were observed 2 weeks after grafting, and greatly increased in number, extending into the distal stump 4 weeks after grafting. Then, based on these finding, long grafts(5〜6 cm)were transplanted into the rabbit sciatic nerve. Four weeks after grafting, numerous regenerating fibers extended into the distal stump. Electrophysiology demonstrated that tibialis anterior muscle was reinnervated both at motor endplates and at muscle spindles.The covering of the graft by L-lactic acid caprolacton tube was recognized to be effective for nerve regeneration.Next, the possibility of utilizing the extracellular matrix of human amnion as graft was exa … More mined. The human amnion was treated by 0.01% ficin for removing the epithelial cells, and manufactured into a thin sheet(ACS), which were stored in a sterile condition(0.1% benzalkonium). From these sheets, basically three different types of tubes were manufactured ; (a)tubes 1〜2 mm in diameter, and 7〜10 layers in wall, (b)bundles of thin tubes in 0.2 mm in diameter each, (c)tubes 1〜2mm in diameter with the additional covering by dexon mesh. These tubes(1 cm) were grafted to the rat sciatic nerve, and examined 2〜4 weeks after grafting. Good nerve regeneration was observed in the graft(a), but not in(b)and(c). Electrophysiology showed the good reinnervation occurred in the anterior tibialis muscle 9 months after grafting. This indicates that ACS, when properly manufactured, is a promising material as the graft for the peripheral nerve regeneration.The further study is needed to develop the method by which the collagen matrix is prepared on which the basal laminae can be fully restored, and the way in which the ACS can be rolled into tubes in a wet condition. Less
首先,我们开发了从骨骼肌纤维中去除细胞成分后可以恢复基底层的方法:用洗涤剂(3%十二烷基硫酸钠,2天37℃)处理新鲜的肌肉组织将这种经过清洁剂处理的肌肉组织移植到脊髓神经中,移植后2周观察到许多再生纤维,并且数量大大增加,并在移植后4周延伸至远端残端。然后,根据这些发现,将长移植物(5-6厘米)移植到兔子坐骨神经中,移植后四个星期,大量再生纤维延伸到远端残端,电生理学表明胫骨前肌在运动终板和神经处都得到了重新支配。 L-乳酸己内酯管覆盖移植物被认为对神经再生有效。接下来,利用人类细胞外基质的可能性羊膜作为移植物是用0.01%无花果素处理的,以去除上皮细胞,并制成薄片(ACS),并在无菌条件下保存(0.1%苯扎氯铵)。 ,基本上制造了三种不同类型的管;(a)直径1~2毫米,壁7~10层的管,(b)细管束每个直径0.2毫米,(c)直径1~2毫米的管,并额外覆盖有dexon网,将这些管(1厘米)移植到大鼠坐骨神经上,并在移植后2~4周检查神经再生良好。在移植物 (a) 中观察到,但在 (b) 和 (c) 中未观察到,电生理学显示移植后 9 个月,胫骨前肌发生了良好的神经支配。一种有前途的周围神经再生移植材料。需要进一步研究开发可以完全恢复基底层的胶原基质的制备方法,以及ACS的滚动方式较少进入潮湿条件下的管中。

项目成果

期刊论文数量(35)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Mligilische,N.,Tabata,Y., et al.: "Peripheral nerve regeneration through a long detergent-denatured antagraft in rabbits."Neuro Report. (印刷中).
Mligilische,N.,Tabata,Y.,等人:“通过长去污剂变性的抗移植物在兔子中再生周围神经”(神经报告)。
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Mligiliche N., Tabata Y., Endoh K.and Ide C.: "Peripheral nerve regeneration through a long detergent-denatured muscle autografts in rabbits."NeuroReport.. 12. 1719-22 (2001)
Mligiliche N.、Tabata Y.、Endoh K. 和 Ide C.:“通过长去污剂变性的兔子自体肌肉移植实现周围神经再生。”NeuroReport.. 12. 1719-22 (2001)
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Ide, C., Mizoguchi, A., Morihara, T., Kawano, S., Fujimoto, E., Hayakashi, T., Tsujihara, T., Shirasu, M., Kimura, K., and Kitada, M.: "Peripheral nerve regeneration."Neural Development Springer. 501-505 (1999)
Ide, C.、Mizoguchi, A.、Morihara, T.、Kawano, S.、Fujimoto, E.、Hayakashi, T.、Tsujihara, T.、Shirasu, M.、Kimura, K. 和 Kitada, M.
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    0
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Morihara T., Mizoguchi A and Ide C.: "Distribution of synaptosomal associated protein 25 in nerve growth cones and reduction of neurite outgrowth by botulinum neurotoxin A without altering growth cone morphology on dorsal root ganglion neurons."Neuroscien
Morihara T.、Mizoguchi A 和 Ide C.:“突触体相关蛋白 25 在神经生长锥中的分布以及肉毒杆菌神经毒素 A 减少神经突生长,而不改变背根神经节神经元的生长锥形态。”Neuroscien
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Ide, C., Mizoguchi, A., Morihara, T., et al: "Neural Development, Keio University Symposium for Life Science and Medicine(Eds, K.Uyemura, K., Kawamura, and T.Yazaki), Springer,"Peripheral nerve regeneration.. pp.501-505 (1999)
Ide, C.、Mizoguchi, A.、Morihara, T. 等人:“神经发育,庆应义塾大学生命科学与医学研讨会(编辑,K.Uyemura, K.、Kawamura 和 T.Yazaki),Springer,
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IDE Chizuka其他文献

IDE Chizuka的其他文献

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{{ truncateString('IDE Chizuka', 18)}}的其他基金

Mechanisms of spinal cord regeneration by transplantation of matured animal-derived somatic stem cells
成熟动物源性成体干细胞移植脊髓再生机制
  • 批准号:
    23300125
  • 财政年份:
    2011
  • 资助金额:
    $ 4.61万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Cell transplantation for the treatment of spinal cord injury in rats-morphological study and search for humoral effective factors-
细胞移植治疗大鼠脊髓损伤-形态学研究及体液有效因子的寻找-
  • 批准号:
    20300122
  • 财政年份:
    2008
  • 资助金额:
    $ 4.61万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Promotion of brain-and spinal-cord regeneration by transplantation of somatic cells(bone marrow stromal cells and choroid plexus ependymal cells)-mechanisms of rescuing injured neural cells, and perspectives for clinical applications-
体细胞(骨髓基质细胞、脉络丛室管膜细胞)移植促进脑脊髓再生-拯救受损神经细胞的机制及临床应用前景-
  • 批准号:
    17300110
  • 财政年份:
    2005
  • 资助金额:
    $ 4.61万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Establishment of adult rat-derived stem cells, and histological/functional reconstruction of spinal cord by auto- and allo-grafting of those stem cells
建立成年大鼠来源的干细胞,并通过这些干细胞的自体和同种异体移植进行脊髓的组织学/功能重建
  • 批准号:
    15300114
  • 财政年份:
    2003
  • 资助金额:
    $ 4.61万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Facilitation of central nerve regeneration by choroid plexus ependymal cells
脉络丛室管膜细胞促进中枢神经再生
  • 批准号:
    12480226
  • 财政年份:
    2000
  • 资助金额:
    $ 4.61万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Study on the condition for central nerve regeneration-grafting of ependymal cells and cell proliferation by neuregulin-
神经调节素促进中枢神经再生-室管膜细胞移植及细胞增殖条件的研究
  • 批准号:
    10470005
  • 财政年份:
    1998
  • 资助金额:
    $ 4.61万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Axon-Schwann cell relationship in nerve regeneration and the mechanisms for the promotion of nerve
神经再生中轴突-雪旺细胞的关系及促进神经的机制
  • 批准号:
    08457004
  • 财政年份:
    1996
  • 资助金额:
    $ 4.61万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Expression of vesicle-associated proteins during the course of differentiation of growth cones into synaptic terminals in nerve regeneration (synaptophysin, synaptotagmin, protein kinase C,etc)
神经再生过程中生长锥分化为突触末梢过程中囊泡相关蛋白的表达(突触素、突触结合蛋白、蛋白激酶C等)
  • 批准号:
    06454142
  • 财政年份:
    1994
  • 资助金额:
    $ 4.61万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)
Mechanisms of regenerating spout formation and growth in the peripheral nerves as studied by confocal laser scanning and immunoelectron microscopy
通过共焦激光扫描和免疫电子显微镜研究周围神经再生喷口形成和生长的机制
  • 批准号:
    04454126
  • 财政年份:
    1992
  • 资助金额:
    $ 4.61万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)
MODEL OF NERVE FIBER REGENERATION IN CNS BY EXCIMER LASER
准分子激光中枢神经系统神经纤维再生模型
  • 批准号:
    02557002
  • 财政年份:
    1990
  • 资助金额:
    $ 4.61万
  • 项目类别:
    Grant-in-Aid for Developmental Scientific Research (B)

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