MORPHOLOGICAL AND PHYSIOLOGICAL STUDY ON EFFECTS OF ELECTRIC STIMULATION ON PERIPHERAL NEURO-MUSCULAR PARALYSIS.

电刺激对周围神经肌肉麻痹影响的形态学和生理学研究。

基本信息

  • 批准号:
    09671494
  • 负责人:
  • 金额:
    $ 2.3万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 财政年份:
    1997
  • 资助国家:
    日本
  • 起止时间:
    1997 至 1998
  • 项目状态:
    已结题

项目摘要

Repairing process and effects of electric stimulation on nerve regeneration were electron microscopically studied at the proximal stump of the transected mouse sciatic nerve. Accumulation of cell organelles (terminal accumulation) and formation of demarcation membranes began soon after transection at the proximal stump. But the vesicle- accumulated portions could not survive for long in the myelin sheath. It appears that vesicle accumulation, formation of the demarcation membranes and degeneration of the vesicle-accumulated portions might be repeated as far as the axon stumps are enclosed by myelin sheath. This repairing process might be very important to minimize the destructive changes which night be caused by exogenic factors, and with this measure, the living axonal portions are always separated from the degenerating portions which are eventually cast off.Axonal sprout formation began 5-6 hours after transection at the node of Ranvier locating just proximal to the cut end. Regenera … More ting axons extensed distally between the myellin sheath and basal lamina of Schwann cells. Electric stimulation was performed soon after the transection. But the axonal sprouting occurred at the node of Ranvier 6 hours after the transection. There were no significant differences in the early process of nerve regeneration between experimental and control groups. both 6 hours or one day after transection. The electric stimulation was performed two days after transection. In the controls. many regenerating axons extended distally beyond , the cut end. Almost all regenerating axons appeared to be morphologically normal. Three hours after the electric stimulation, destructive changes such as rupure of vesicles and mitochondria, formation of multivesicular bodies and lysosomes were observed only in some growth cones of the regenerating axons. One day after the stimulation, there were no significant differences in nerve regeneration between the experimental and control groups. These findings suggest that the electric stimulation might affect only transiently and mainly on nascent growth cones. Less
通过电子显微镜研究了横断小鼠坐骨神经近端残端的修复过程和电刺激对神经再生的影响。在近端残端横断后不久,细胞器的积累(末端积累)和分界膜的形成就开始了。但囊泡积累的部分不能在髓鞘中长期存活。看来,只要轴突残端被髓鞘包围,囊泡积累、分界膜的形成和囊泡积累部分的变性可能会重复。这种修复过程对于最大限度地减少外源因素造成的破坏性变化可能非常重要,通过这种措施,活的轴突部分总是与最终脱落的退化部分分离。轴突芽形成在横断后 5-6 小时开始,位于紧邻切割端的 Ranvier 节点。再生轴突在雪旺细胞的髓鞘和基底层之间向远端延伸。横断后不久进行电刺激。但横断后6小时,Ranvier结处出现轴突出芽。实验组和对照组神经再生的早期过程没有显着差异。横切后 6 小时或一天。横断后两天进行电刺激。在控件中。许多再生轴突向远端延伸超出切割端。几乎所有再生轴突的形态均正常。电刺激三小时后,仅在再生轴突的一些生长锥中观察到破坏性变化,例如囊泡和线粒体的破裂、多囊泡体和溶酶体的形成。刺激一天后,实验组和对照组之间的神经再生没有显着差异。这些发现表明,电刺激可能只会短暂地影响,并且主要影响新生的生长锥。较少的

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
A.Miki,T.Matsubara,and Y.Kohbu: "Repairing process at the proximal stump of myelinated axons, with special reference to fomation of the demarcaion memboanes." Bull.Health Sci. Kobe. 14. 11-23 (1998)
A.Miki、T.Matsubara 和 Y.Kohbu:“有髓轴突近端残端的修复过程,特别是分界膜的形成。”
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
A.Miki, T.Matsubara, and Y.Khobu: "Repaining process at the proximal stuanp of myelinated arons, with special reference to formation of the demar cation membranes." Ball. Health Sci, Kobe. 14. 11-23 (1998)
A.Miki、T.Matsubara 和 Y.Khobu:“有髓鞘近端的修复过程,特别是分界膜的形成。”
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
AKINORI MIKI,TAKAKO MATSUBARA,YOSHIHIDE KOHBU: "REPAIRING PROCESS AT THE PROXIMAL STUMP OF TRANSECTED MYELINATED AXONS,WITH SPECIAL REFERENCE TO FORMATION OF THE DEMARCATION MEMBRANES" BULL.HEALTH SCI.KOBE. 14. 11-23 (1998)
AKINORI MIKI、TAKAKO MATSUBARA、YOSHIHIDE KOHBU:“横断髓鞘轴突近端残端的修复过程,特别参考分界膜的形成”BULL.HEALTH SCI.KOBE。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

MIKI Akinori其他文献

MIKI Akinori的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('MIKI Akinori', 18)}}的其他基金

Reconsideration of physical approach for skeletal muscle injury
重新考虑骨骼肌损伤的物理方法
  • 批准号:
    22500460
  • 财政年份:
    2010
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Effects of physicul stimulation and some growth factors on peripheral nerve regeneration and muscle strophy.
物理刺激和一些生长因子对周围神经再生和肌肉萎缩的影响。
  • 批准号:
    18500403
  • 财政年份:
    2006
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Effects of physical stimulations on regeneration of peripheral nerves and denervated muscle fibers
物理刺激对周围神经和失神经肌纤维再生的影响
  • 批准号:
    16500342
  • 财政年份:
    2004
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Influence of electrical and electromagnetic stimulation on peripheral nerve regeneration
电和电磁刺激对周围神经再生的影响
  • 批准号:
    12832025
  • 财政年份:
    2000
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)

相似海外基金

Targeting the microtubule cytoskeleton to promote cavernous nerve regeneration and erectile function after injury
靶向微管细胞骨架促进损伤后海绵体神经再生和勃起功能
  • 批准号:
    10719124
  • 财政年份:
    2023
  • 资助金额:
    $ 2.3万
  • 项目类别:
Novel growth factors and regenerative RGC subtypes for optic nerve regeneration
用于视神经再生的新型生长因子和再生 RGC 亚型
  • 批准号:
    10666784
  • 财政年份:
    2023
  • 资助金额:
    $ 2.3万
  • 项目类别:
Ectopic Olfactory Receptor Guided Facial Nerve Regeneration
异位嗅觉受体引导面神经再生
  • 批准号:
    10575837
  • 财政年份:
    2023
  • 资助金额:
    $ 2.3万
  • 项目类别:
Development of optimal nerve suture method not interfere with nerve regeneration after nerve repair surgery
开发最佳神经缝合方法,不干扰神经修复手术后的神经再生
  • 批准号:
    23K15625
  • 财政年份:
    2023
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
Basic research for nerve regeneration using novel functional peptide loaded artificial nerve
新型功能肽负载人工神经神经再生的基础研究
  • 批准号:
    23K09098
  • 财政年份:
    2023
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Axon Regeneration-Associated Gene Enhancers Promoting Successful CNS Nerve Regeneration
轴突再生相关基因增强剂促进中枢神经系统神经再生成功
  • 批准号:
    10511016
  • 财政年份:
    2023
  • 资助金额:
    $ 2.3万
  • 项目类别:
The role of Taf7l and Fscn1 in peripheral nerve regeneration
Taf7l和Fscn1在周围神经再生中的作用
  • 批准号:
    23K08674
  • 财政年份:
    2023
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Development of biofunctionalised graphene nerve conduits (NerveGraft) for nerve regeneration
开发用于神经再生的生物功能化石墨烯神经导管(NerveGraft)
  • 批准号:
    10072550
  • 财政年份:
    2023
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Collaborative R&D
Regulation of successful optic nerve regeneration by the mevalonate/cholesterol pathway
甲羟戊酸/胆固醇途径成功调节视神经再生
  • 批准号:
    10500994
  • 财政年份:
    2022
  • 资助金额:
    $ 2.3万
  • 项目类别:
Multiple approaches for optic nerve regeneration in rat optic nerve crush models
大鼠视神经挤压模型中视神经再生的多种方法
  • 批准号:
    22K09829
  • 财政年份:
    2022
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了