J Brachial Plex Peripher Nerve Inj 2011; 06(01): e11-e22
DOI: 10.1186/1749-7221-6-4
Research article
Stecker et al; licensee BioMed Central Ltd.

Acute nerve stretch and the compound motor action potential[*]

Mark M Stecker
1   Department of Neuroscience, Marshall University School of Medicine, Huntington, WV 25701 USA
,
Kelly Baylor
1   Department of Neuroscience, Marshall University School of Medicine, Huntington, WV 25701 USA
,
Jacob Wolfe
1   Department of Neuroscience, Marshall University School of Medicine, Huntington, WV 25701 USA
,
Matthew Stevenson
1   Department of Neuroscience, Marshall University School of Medicine, Huntington, WV 25701 USA
› Author Affiliations

Subject Editor:
Further Information

Publication History

25 July 2010

24 August 2011

Publication Date:
23 September 2014 (online)

Abstract

In this paper, the acute changes in the compound motor action potential (CMAP) during mechanical stretch were studied in hamster sciatic nerve and compared to the changes that occur during compression.

In response to stretch, the nerve physically broke when a mean force of 331 gm (3.3 N) was applied while the CMAP disappeared at an average stretch force of 73 gm (0.73 N). There were 5 primary measures of the CMAP used to describe the changes during the experiment: the normalized peak to peak amplitude, the normalized area under the curve (AUC), the normalized duration, the normalized velocity and the normalized velocity corrected for the additional path length the impulses travel when the nerve is stretched. Each of these measures was shown to contain information not available in the others.

During stretch, the earliest change is a reduction in conduction velocity followed at higher stretch forces by declines in the amplitude of the CMAP. This is associated with the appearance of spontaneous EMG activity. With stretch forces < 40 gm (0.40 N), there is evidence of increased excitability since the corrected velocities increase above baseline values. In addition, there is a remarkable increase in the peak to peak amplitude of the CMAP after recovery from stretch < 40 gm, often to 20% above baseline.

Multiple means of predicting when a change in the CMAP suggests a significant stretch are discussed and it is clear that a multifactorial approach using both velocity and amplitude parameters is important. In the case of pure compression, it is only the amplitude of the CMAP that is critical in predicting which changes in the CMAP are associated with significant compression.

*This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


 
  • References

  • 1 Stecker MM, Baylor K, Chan YM. Acute nerve compression and the compound muscle action potential. J Brachial Plex Peripher Nerve Inj 2008; 3: 1 10.1186/1749-7221-3-1 2245939 18211681
  • 2 Abe I, Tsujino A, Hara Y, Ichimura H, Ochiai N. Paranodal demyelination by gradual nerve stretch can be repaired by elongation of internodes. Acta Neuropathol 2002; 104 (5) 505-512 12410398
  • 3 Haftek J. Stretch injury of peripheral nerve. Acute effects of stretching on rabbit nerve. J Bone Joint Surg Br 1970; 52 (2) 354-365 5445417
  • 4 Maxwell WL, Kosanlavit R, McCreath BJ, Reid O, Graham DI. Freeze-fracture and cytochemical evidence for structural and functional alteration in the axolemma and myelin sheath of adult guinea pig optic nerve fibers after stretch injury. J Neurotrauma 1999; 16 (4) 273-284 10.1089/neu.1999.16.273 10225214
  • 5 Jafari SS, Nielson M, Graham DI, Maxwell WL. Axonal cytoskeletal changes after nondisruptive axonal injury. II. Intermediate sized axons. J Neurotrauma 1998; 15 (11) 955-966 10.1089/neu.1998.15.955 9840768
  • 6 Maxwell WL, Graham DI. Loss of axonal microtubules and neurofilaments after stretch-injury to guinea pig optic nerve fibers. J Neurotrauma 1997; 14 (9) 603-614 10.1089/neu.1997.14.603 9337123
  • 7 Ikeda K, Tomita K, Tanaka S. Experimental study of peripheral nerve injury during gradual limb elongation. Hand Surg 2000; 5 (1) 41-47 10.1142/S0218810400000028 11089187
  • 8 Brown R, Pedowitz R, Rydevik B, Woo S, Hargens A, Massie J, Kwan M, Garfin SR. Effects of acute graded strain on efferent conduction properties in the rabbit tibial nerve. Clin Orthop Relat Res 1993; 288-294 (296)(296)
  • 9 Wall EJ, Massie JB, Kwan MK, Rydevik BL, Myers RR, Garfin SR. Experimental stretch neuropathy. Changes in nerve conduction under tension. J Bone Joint Surg Br 1992; 74 (1) 126-129 1732240
  • 10 Li J, Shi R. Stretch-induced nerve conduction deficits in guinea pig ex vivo nerve. J Biomech 2007; 40 (3) 569-578 10.1016/j.jbiomech.2006.02.009 16674962
  • 11 Fowler SS, Leonetti JP, Banich JC, Lee JM, Wurster R, Young MR. Duration of neuronal stretch correlates with functional loss. Otolaryngol Head Neck Surg 2001; 124 (6) 641-644 10.1067/mhn.2001.115908 11391254
  • 12 Katz B, Miledi R. The effect of temperature on the synaptic delay at the neuromuscular junction. J Physiol 1965; 181 (3) 656-670 1357674 5880384
  • 13 Moller AR. Intra-Opeative Neurophysiologic Monitoring. Humana Press; Totowa, NJ: 2005
  • 14 Stecker MM, Cheung AT, Patterson T, Savino JS, Weiss SJ, Richards RM, Bavaria JE, Gardner TJ. Detection of stroke during cardiac operations with somatosensory evoked responses. J Thorac Cardiovasc Surg 1996; 112 (4) 962-972 10.1016/S0022-5223(96)70096-X 8873722
  • 15 Neuloh G, Schramm J. Are there false-negative results of motor evoked potential monitoring in brain surgery?. Cen Eur Neurosurg 2009; 70 (4) 171-175 10.1055/s-0029-1225651 19851956
  • 16 Krammer MJ, Wolf S, Schul DB, Gerstner W, Lumenta CB. Significance of intraoperative motor function monitoring using transcranial electrical motor evoked potentials (MEP) in patients with spinal and cranial lesions near the motor pathways. Br J Neurosurg 2009; 23 (1) 48-55 10.1080/02688690802563349 19234909
  • 17 Keyhani K, Miller CC, Estrera AL, Wegryn T, Sheinbaum R, Safi HJ. Analysis of motor and somatosensory evoked potentials during thoracic and thoracoabdominal aortic aneurysm repair. J Vasc Surg 2009; 49 (1) 36-41 10.1016/j.jvs.2008.08.005 18829232
  • 18 More RC, Nuwer MR, Dawson EG. Cortical evoked potential monitoring during spinal surgery: sensitivity, specificity, reliability, and criteria for alarm. J Spinal Disord 1988; 1 (1) 75-80 2980065
  • 19 Jou IM, Lai KA, Shen CL, Yamano Y. Changes in conduction, blood flow, histology, and neurological status following acute nerve-stretch injury induced by femoral lengthening. J Orthop Res 2000; 18 (1) 149-155 10.1002/jor.1100180121 10716291
  • 20 Sachs F. Stretch-activated ion channels: what are they?. Physiology (Bethesda) 2010; 25 (1) 50-56
  • 21 Quasthoff S. A mechanosensitive K+ channel with fast-gating kinetics on human axons blocked by gadolinium ions. Neurosci Lett 1994; 169 (1-2) 39-42 10.1016/0304-3940(94)90351-4 8047289
  • 22 Lin YW, Cheng CM, Leduc PR, Chen CC. Understanding sensory nerve mechanotransduction through localized elastomeric matrix control. PLoS One 2009; 4 (1) e4293 10.1371/journal.pone.0004293 2627935 19173000
  • 23 Lundbaek JA, Birn P, Hansen AJ, Sogaard R, Nielsen C, Girshman J, Bruno MJ, Tape SE, Egebjerg J, Greathouse DV, Mattice GL, Koeppe RE, Andersen OS. Regulation of sodium channel function by bilayer elasticity: the importance of hydrophobic coupling. Effects of Micelle-forming amphiphiles and cholesterol. J Gen Physiol 2004; 123 (5) 599-621 10.1085/jgp.200308996 2234500 15111647
  • 24 Baylor K, Stecker MM. Peripheral nerve at extreme low temperatures 2: pharmacologic modulation of temperature effects. Cryobiology 2009; 59 (1) 12-18 10.1016/j.cryobiol.2009.01.006 19558973
  • 25 Shi R, Blight AR. Differential effects of low and high concentrations of 4-aminopyridine on axonal conduction in normal and injured spinal cord. Neuroscience 1997; 77 (2) 553-562 10.1016/S0306-4522(96)00477-0 9472411
  • 26 Lundborg G, Rydevik B. Effects of stretching the tibial nerve of the rabbit: A preliminary stud of the intraneural ciruculation and the barrier function of the perineurium. J Bone and Joint Surgery 1973; 55-B (02) 390-401
  • 27 Liu CT, Benda CE, Lewey FH. Tensile strength of human nerves; an experimental physical and histologic study. Arch Neurol Psych 1948; 59 (3) 322-336