Suppr超能文献

延迟周围神经修复后功能恢复减弱的基础。

The basis for diminished functional recovery after delayed peripheral nerve repair.

机构信息

Centre for Neuroscience, Department of Medicine and Dentistry, University of Alberta, Edmonton, Alberta T6G 2S2, Canada.

出版信息

J Neurosci. 2011 Apr 6;31(14):5325-34. doi: 10.1523/JNEUROSCI.6156-10.2011.

Abstract

The postsurgical period during which neurons remain without target connections (chronic axotomy) and distal nerve stumps and target muscles are denervated (chronic denervation) deleteriously affects functional recovery. An autologous nerve graft and cross-suture paradigm in Sprague Dawley rats was used to systematically and independently control time of motoneuron axotomy, denervation of distal nerve sheaths, and muscle denervation to determine relative contributions of each factor to recovery failure. Tibial (TIB) nerve was cross-sutured to common peroneal (CP) nerve via a contralateral 15 mm nerve autograft to reinnervate the tibialis anterior (TA) muscle immediately or after prolonging TIB axotomy, CP autograft denervation, or TA muscle denervation. Numbers of motoneurons that reinnervated TA muscle declined exponentially from 99 ± 15 to asymptotic mean (± SE) values of 35 ± 1, 41 ± 10, and 13 ± 5, respectively. Enlarged reinnervated motor units fully compensated for reduced motoneuron numbers after prolonged axotomy and autograft denervation, but the maximal threefold enlargement did not compensate for the severe loss of regenerating nerves through chronically denervated nerve stumps and for failure of reinnervated muscle fibers to recover from denervation atrophy. Muscle force, weight, and cross-sectional area declined. Our results demonstrate that chronic denervation of the distal stump plays a key role in reduced nerve regeneration, but the denervated muscle is also a contributing factor. That chronic Schwann cell denervation within the nerve autograft reduced regeneration less than after the denervation of both CP nerve stump and TA muscle, argues that chronic muscle denervation negatively impacts nerve regeneration.

摘要

术后神经元失去靶连接(慢性轴索切断)和远端神经末梢及靶肌肉失神经支配(慢性去神经支配)的时期对功能恢复有不利影响。我们采用 Sprague Dawley 大鼠自体神经移植和交叉缝合范例,系统且独立地控制运动神经元轴索切断、远端神经鞘去神经支配和肌肉去神经支配的时间,以确定每个因素对恢复失败的相对贡献。通过对侧 15mm 神经自体移植将胫神经(TIB)交叉缝合至腓总神经(CP),以立即或延长 TIB 轴索切断、CP 自体神经移植去神经支配或 TA 肌肉去神经支配后,重新支配胫骨前肌(TA)。重新支配 TA 肌肉的运动神经元数量从 99 ± 15 呈指数下降至渐近平均值(± SE)分别为 35 ± 1、41 ± 10 和 13 ± 5。延长轴索切断和自体神经移植去神经支配后,增大的再支配运动单位完全补偿了运动神经元数量的减少,但最大三倍的增大并不能补偿因慢性失神经支配的神经末梢导致再生神经的严重损失,也不能补偿因失神经支配的肌肉纤维无法从去神经支配萎缩中恢复而导致的损失。肌肉力量、重量和横截面积下降。我们的结果表明,远端神经末梢的慢性失神经支配在减少神经再生中起着关键作用,但失神经支配的肌肉也是一个促成因素。在 CP 神经末梢和 TA 肌肉失神经支配后,神经自体移植中的慢性施万细胞失神经支配对再生的影响较小,这表明慢性肌肉失神经支配对神经再生有负面影响。

相似文献

引用本文的文献

3
Sonographic evaluation of pediatric traumatic peripheral nerve injuries.小儿外伤性周围神经损伤的超声评估
Pediatr Radiol. 2025 Jul;55(8):1728-1740. doi: 10.1007/s00247-025-06253-y. Epub 2025 Jun 3.
6
Engineering the Future of Restorative Clinical Peripheral Nerve Surgery.塑造修复性临床周围神经外科的未来
Adv Healthc Mater. 2025 Aug;14(20):e2404293. doi: 10.1002/adhm.202404293. Epub 2025 Apr 1.

本文引用的文献

6
Clinical application of sensory protection of denervated muscle.失神经肌肉感觉保护的临床应用
J Neurosurg. 2008 Nov;109(5):955-61. doi: 10.3171/JNS/2008/109/11/0955.
9
Pleiotrophin is a neurotrophic factor for spinal motor neurons.多效生长因子是脊髓运动神经元的一种神经营养因子。
Proc Natl Acad Sci U S A. 2007 Mar 13;104(11):4664-9. doi: 10.1073/pnas.0603243104. Epub 2007 Mar 5.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验