Neuromuscular Junction Integrity after Chronic Nerve Compression Injury

被引:14
|
作者
Mozaffar, Tahseen [2 ,4 ]
Strandberg, Erika [1 ,4 ]
Abe, Kazuko [1 ,4 ]
Hilgenberg, Lutz G. [3 ]
Smith, Martin A. [3 ]
Gupta, Ranjan [1 ,3 ,4 ]
机构
[1] Dept Orthopaed, Orange, CA 92868 USA
[2] Dept Neurol, Orange, CA 92868 USA
[3] Univ Calif Irvine, Dept Neurobiol & Anat, Irvine, CA 92697 USA
[4] Univ Calif Irvine, Peripheral Nerve Res Lab, Gillespie Neurosci Res Facil 2226, Irvine, CA 92697 USA
关键词
chronic nerve injury; demyelination; motor unit; axonal sprouts; MYELIN-ASSOCIATED GLYCOPROTEIN; CARPAL-TUNNEL-SYNDROME; SCHWANN-CELLS; ACETYLCHOLINE-RECEPTORS; MACROPHAGE RECRUITMENT; DEMYELINATION; DEGENERATION; INHIBITION; EXPRESSION; OUTGROWTH;
D O I
10.1002/jor.20704
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Chronic nerve compression injuries (CNC) are progressive demyelinating disorders characterized by a gradual decline of the nerve conduction velocity (NCV) in the affected nerve region. CNC injury induces a robust Schwann cell response with axonal sprouting, but without morphologic evidence of axonal injury. We hypothesize that early CNC injury occurs without damage to neuromuscular junction of motor axon. A well-established animal model was used to assess for damage to motor axons. As sprouting is considered a hallmark of regeneration during and after axonal degeneration and sprouting was confirmed Visually at 2 weeks in CNC animals, we assessed for axonal degeneration in motor nerves after CNC by evaluating the integrity of the neuromuscular junction. NCV exhibited a gradual progressive decline consistent with the human condition. Compound motor action potential amplitudes decreased slightly immediately and plateaued, indicating that there was not sustained and increasing axonal loss. Sprouting was confirmed using immunofluorescence and by an increase in number of unmyelinated axons and Remak bundles. Blind analysis of the neuromuscular junction showed no difference between control and CNC images, indicating that there was no evidence for end-unit axonal loss in the soleus muscle. Because the progressive decline in NCV was not paired with a similar progressive decline in amplitude, it is likely that axonal loss is not responsible for slowing of action potentials. Blind analysis of the neuromuscular junction provides further evidence that the axonal sprouting seen early after CNC injury is not a consequence of axonal degeneration in the motor nerves. (C) 2008 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 27:114-119, 2009
引用
收藏
页码:114 / 119
页数:6
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