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一种增强传统修复外周神经再生的方法。

A method of enhancing regeneration of conventionally repaired peripheral nerves.

作者信息

Demirkan F, Snyder C C, Latifoglu O, Siemionow M

机构信息

University of Gazi, Department of Plastic Surgery, Besevler, Ankara, Turkey.

出版信息

Ann Plast Surg. 1995 Jan;34(1):67-72. doi: 10.1097/00000637-199501000-00013.

DOI:10.1097/00000637-199501000-00013
PMID:7535514
Abstract

The effect of axoplasmic fluid injection on regeneration of conventionally repaired nerve was studied. Twenty New Zealand rabbits were studied in two experimental groups: immediate nerve repair (Group 1A, no axoplasm; Group 1B, axoplasm injection) and delayed nerve repair (Group 2A, no axoplasm; Group 2B, axoplasm injection group). A total of 40 sciatic nerve repairs were performed. After epineurial nerve repair, axoplasmic fluid collected from the proximal and distal nerve stumps was injected under epineurium proximally and distally to the anastomotic site. In the two control groups (immediate nerve repair and delayed nerve repair, both without axoplasm), 0.9% saline was injected in a similar way. Nerve regeneration was assessed by measuring hair and nail growth, plantar and dorsal foot temperature, muscle atrophy, and the toe spread test. In the 3- and 6-month follow-up periods, nerve samples were taken for histological evaluation. Specimens were stained with toluidine blue, and 50% of the nerve cross-section area was counted from microphotographic reconstructions. After immediate repair in Group 1, axoplasmic fluid-treated animals showed a 27% increase in the number of myelinated axons at 3 months when compared with saline-treated controls (3,768 vs. 2,962 +/- 1,921 SD). After delayed repair in Group 2, a 32% increase in myelination axon counts was detected at 3 months in axoplasm-treated animals compared with saline-injected controls (1,040 +/- 684 SD vs. 786 +/- 389 SD). In addition, a positive toe spread test result was seen at 6 months in the axoplasmic fluid-treated animals.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了轴浆注射对传统修复神经再生的影响。将20只新西兰兔分为两个实验组:即时神经修复组(1A组,未注射轴浆;1B组,注射轴浆)和延迟神经修复组(2A组,未注射轴浆;2B组,注射轴浆组)。共进行了40次坐骨神经修复。在神经外膜修复后,将从近端和远端神经残端收集的轴浆注射到吻合部位近端和远端的神经外膜下。在两个对照组(即时神经修复和延迟神经修复,均未注射轴浆)中,以类似方式注射0.9%生理盐水。通过测量毛发和指甲生长、足底和足背温度、肌肉萎缩以及趾展试验来评估神经再生。在3个月和6个月的随访期内,采集神经样本进行组织学评估。标本用甲苯胺蓝染色,并从显微照片重建中计算神经横截面积的50%。在1组即时修复后,与生理盐水处理的对照组相比,接受轴浆处理的动物在3个月时髓鞘化轴突数量增加了27%(3768对2962±1921标准差)。在2组延迟修复后,与注射生理盐水的对照组相比,接受轴浆处理的动物在3个月时髓鞘化轴突计数增加了32%(1040±684标准差对786±389标准差)。此外,接受轴浆处理的动物在6个月时趾展试验结果为阳性。(摘要截断于250字)

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