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电场对神经再生微环境中活性蛋白的影响 被引量:2

Effect of electric fields on the protein in nerve regen-eration conditioned fluid
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摘要 为探讨电场对神经再生的影响,作者采用神经再生室模型,将大鼠分四组:局部神经干电刺激组(L组);脊髓神经元电刺激组(N组);(失神经)肌肉电刺激组(M组);对照组(C组)。于术后3、7、14、21、28天,用微量进样器抽取神经再生条件液,进行100×103分子量以下分子量区域的蛋白电泳与定量扫描分析。实验结果显示:L组在6.16~10.23×103分子量区域,其蛋白含量显著高于其它组,其它组之间差异无显著性。认为此变化是电场促进神经再生的可能原因之一。 0 SD rats were randomly divided into four groupsof 20 each:local electrostimulation of nerve stump(Group LS) ; electro-stimulation of myeloneure (GroupN ); electrostimulation of the denervated muscle(Group M) ;and controls (Group C). The left lateralsciatic nerve of rats was excised smin in length, andthe severed nerve was bridged with the silicon tube.The gap between the sturnps was about 10mm. At3rd, 7th , 14th , 21st and 28th day after nerve transec-tion and tube implantation, the fluid in the silicon tubewas aspirated. The sample of fluid was spun and 4μlaliquots were taken from the supernatant. Then theelectrophoresis of the aliquots was made by phasesys-tem and assayed to the amount and variety by Gel Scansystem. The results showed that the group LS had ahigh increase in the protein amount than others in therange of 6. 16~10. 23 × 103 D molecular weight. Webelieve that it is one of the mechanisms of the electricfields promoting nerve regeneration.
出处 《中华医学杂志》 CAS CSCD 北大核心 1995年第8期470-472,共3页 National Medical Journal of China
基金 国家自然科学基金
关键词 神经再生 电刺激 活性蛋白 蛋白质 小鼠 Nerve regeneration Electro stim-ulation Protein analysis
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参考文献3

  • 1王玉江,神经解剖学杂志,1992年,8卷,163页
  • 2董永泉,中华外科杂志,1992年,30卷,313页
  • 3沈宁江,中华显微外科杂志,1992年,16卷,116页

同被引文献14

  • 1沈宁江,王宇田,樊红灿.直流电场与汉防己甲素联合应用对急性脊髓损伤的保护作用及其机制(英文)[J].中国临床康复,2004,8(35):8109-8111. 被引量:1
  • 2Dubenard JM, Owen E, Herzberg G, et al. Human hand allograft:report on first 6 months, lancet, 1999,353:1315-1320.
  • 3Gold BG, Storm-Dickerson T, Austin DR, et al. FKS06, an immunosuppressant, increases functional recovery and axonal regeneration in the rat following axotomy of the sciatic nerve. Soc Neurosci Abstr, 1993,19 : 1316.
  • 4Schreiber SL, Crabtree GR. The Mechanism of cyclospofin A and FKS06. lmmunol Today, 1992,13:136-142.
  • 5Steiner JP, Dawson TM, Fotuhi M, et al. High brain densities of the immunophilin FKBP colocalized with calneufin. Nature, 1992,358:584-587.
  • 6Dowson TM, Steiner JP, Lyons WE, et al. The immunophilins,FK506 binding protein and eyclophilin, are discretely localized in the brain : relationship to calcineufin. Neuroscience, 1994, 62 : 569-580.
  • 7Wang MS, Zeleny-Pooley M, Gold BG. Comparative dose-dependece study of FK506 and cyclospofin A on the rate of axonal regeneration in rat sciatic nerve. J Pharmacol Exp Ther, 1997,282:1084-1093.
  • 8Steiner JP, Hamilton GS, Ross DT, et al. Neurotrophic immunophilin ligands stimulate structural and functional recovery in neurodegenerative animal models. Proc Natl Acad Sci USA, 1997,94 : 2019 -2024.
  • 9Gold BG. FK506 and the role of the immunophilin FKBP-52 in nerve regeneration. Drug Metablism Reviews, 1999,31,649-663.
  • 10Lyons WE, George EB, Dawson TM, et al. Immunosuppressant FKS06 promotes neurite outgrowth in cultures of PC-12 cells and sensory ganglia. Proc Natl Acad Sci USA, 1994,91:3191-3195.

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