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作 者:刘丹[1,2] 胡文[2] 张燕平[1,2] 邓爱东[1] 顾剑辉[1]
机构地区:[1]南通大学附属医院手外科,南通226001 [2]南通大学神经再生重点实验室,南通226001
出 处:《解剖学杂志》2013年第3期350-352,共3页Chinese Journal of Anatomy
基 金:国家自然科学基金(81100939);江苏省高校自然科学基金(10KJB310009),江苏省普通高校研究生科研创新计划项目(CXZZ12-0872);南通大学研究生科技创新计划项目(YKC12007)
摘 要:目的:探讨神经示踪剂荧光金(FG)、真蓝(TB)和荧光红(FR)两两组合对脊髓运动神经元的标记效率差异,为再生神经重支配准确性研究奠定基础。方法:采用大鼠胫神经示踪模型,采取神经内注射与神经横断后近侧断端浸泡(20min)2种方式,分别对FG、TB和FR的两两组合进行示踪试验。示踪术后5d,取脊髓腰膨大段冷冻纵切,共聚焦显微镜进行显微成像和计数。结果:FG联合TB示踪标记的运动神经元数量最多,其次为FG联合FR,而FR联合TB组标记细胞数最少,双标比例也最小。神经断端浸泡方式使用示踪剂时标记效率仅为神经内注射的2/3左右。结论:FG联合TB以及FG联合FR示踪对脊髓运动神经元的标记效果较好,且神经内注射使用示踪剂效果优子持续20min的神经断端浸泡。Objective: To test the double-labeling efficacy of different combinations of the neural tracers fluoro-gold (FG), true blue (TB) and fluoro-ruby (FR). Methods: The left tibia[ nerve of adult Sprague-Dawley rats was exposed to different tracer combinations, i.e. FG-FR, FG-TB or FR-TB, either by intra-fascicular neural injection or by nerve transection and immediate immersion of the proximal nerve stump into tracer mixture for 20 min. After survival for 5 days, the lumbar enlargement of the spinal cord was dissected out and longitudinally cryo-sectioned under a laser confocal microscope and labeled motor neurons counted. Results: The tracing with a combination of FG and TB gave the largest number of labeled motor neurons, among which 80%-85% was doubly labeled. The combined use of FG and FR also exhibited the second largest number of labeled motor neurons with over 90% double labeling. However, the FR-TB combination group showed poor labeling efficacy in terms of total labeled neurons and double labeling ratio. Exposure to tracers via nerve stump-immersion (20 min) was observed to be significantly less efficient, i.e. 2/3 labeling, than via intra-faseieular neural injeetion. Conclusion: The combination of either FG with TB or FG with FR seemed suitable for sequential retrograde tracing in assessing nerve regeneration aeeuraey, with better labeling efficacy for intra-fascicular neural injection.
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