Effects of high-frequency alternating current on axonal conduction through the vagus nerve

High-frequency alternating current (HFAC) is known to disrupt axonal conduction in peripheral nerves, and HFAC has much potential as a therapeutic approach for a number of pathological conditions. Many previous studies have utilized motor output as a bioassay of effects of HFAC on conduction through medium- to large-diameter motor axons. However, little is known about the effectiveness of HFAC on smaller, more slowly conducting nerve fibres. The present study tested whether HFAC influences axonal conduction through sub-diaphragmatic levels of the rat vagus nerve, which consists almost entirely of small calibre axons. Using an isolated nerve preparation, we tested the effects of HFAC on electrically evoked compound action potentials (CAPs). We found that delivery of charge-balanced HFAC at 5000 Hz for 1 min was effective in producing reversible blockade of axonal conduction. Both Aδ and C components of the vagus CAP were attenuated, and the degree of blockade as well as time to recovery was proportional to the amount of HFAC current delivered. The Aδ waves were more sensitive than C waves to HFAC blockade, but they required more time to recover.

[1]  A. J. Bower,et al.  An electron microscope study of vagus nerve composition in the ferret , 2004, Anatomy and Embryology.

[2]  G. Gebhart,et al.  Mechanosensitive properties of gastric vagal afferent fibers in the rat. , 1999, Journal of neurophysiology.

[3]  Terry L. Powley,et al.  The fiber composition of the abdominal vagus of the rat , 2004, Anatomy and Embryology.

[4]  J Holsheimer,et al.  Morphometry of human superficial dorsal and dorsolateral column fibres: significance to spinal cord stimulation. , 2002, Brain : a journal of neurology.

[5]  R. Docherty,et al.  Differential sensitivity to tetrodotoxin and lack of effect of prostaglandin E2 on the pharmacology and physiology of propagated action potentials , 2002, British journal of pharmacology.

[6]  J. Kral,et al.  Truncal vagotomy in morbid obesity. , 1981, International journal of obesity.

[7]  Richard H. White,et al.  Sex Differences in Sensory and Motor Branches of the Pudendal Nerve of the Rat , 1996, Hormones and Behavior.

[8]  Kevin L Kilgore,et al.  Frequency- and amplitude-transitioned waveforms mitigate the onset response in high-frequency nerve block , 2010, Journal of neural engineering.

[9]  K. Kilgore,et al.  Nerve conduction block utilising high-frequency alternating current , 2004, Medical and Biological Engineering and Computing.

[10]  Stephen T. Foldes,et al.  Simulation of high-frequency sinusoidal electrical block of mammalian myelinated axons , 2007, Journal of Computational Neuroscience.

[11]  L. Dragstedt Vagotomy for gastroduodenal ulcer. , 1945, Annals of surgery.

[12]  Xu Zhang,et al.  Simulation analysis of conduction block in myelinated axons induced by high-frequency biphasic rectangular pulses , 2006, IEEE Transactions on Biomedical Engineering.

[13]  K. Bielefeldt,et al.  Sensitization of mechanosensitive gastric vagal afferent fibers in the rat by thermal and chemical stimuli and gastric ulcers. , 2004, Journal of neurophysiology.

[14]  Changfeng Tai,et al.  Response of external urethral sphincter to high frequency biphasic electrical stimulation of pudendal nerve. , 2005, The Journal of urology.

[15]  Xu Zhang,et al.  Mechanism of Nerve Conduction Block Induced by High-Frequency Biphasic Electrical Currents , 2006, IEEE Transactions on Biomedical Engineering.

[16]  R. Coggeshall,et al.  An analysis of the axon populations in the nerves to the pelvic viscera in the rat , 1982, The Journal of comparative neurology.

[17]  J. Roppolo,et al.  Simulation of nerve block by high-frequency sinusoidal electrical current based on the Hodgkin-Huxley model , 2005, IEEE Transactions on Neural Systems and Rehabilitation Engineering.

[18]  Changfeng Tai,et al.  Block of external urethral sphincter contraction by high frequency electrical stimulation of pudendal nerve. , 2004, The Journal of urology.

[19]  F. Rattay Analysis of models for extracellular fiber stimulation , 1989, IEEE Transactions on Biomedical Engineering.

[20]  Piet Bergveld,et al.  Fascicular Selectivity in Transverse Stimulation with a Nerve Cuff Electrode: A Theoretical Approach , 2003, Neuromodulation : journal of the International Neuromodulation Society.

[21]  H. A. Davenport,et al.  The ratio of myelinated to unmyelinated fibers in regenerated sciatic nerves of Macacus rhesus , 1937 .

[22]  Arthur Prochazka,et al.  Transcutaneously Coupled, High-Frequency Electrical Stimulation of the Pudendal Nerve Blocks External Urethral Sphincter Contractions , 2009, Neurorehabilitation and neural repair.

[23]  H. Schmalbruch,et al.  Fiber composition of the rat sciatic nerve , 1986, The Anatomical record.

[24]  Niloy Bhadra,et al.  High‐frequency electrical conduction block of mammalian peripheral motor nerve , 2005, Muscle & nerve.

[25]  C. Stucky,et al.  Receptive properties of mouse sensory neurons innervating hairy skin. , 1997, Journal of neurophysiology.

[26]  M Y WOO,et al.  ASYNCHRONOUS FIRING AND BLOCK OF PERIPHERAL NERVE CONDUCTION BY 20 KC ALTERNATING CURRENT. , 1964, Bulletin of the Los Angeles Neurological Society.

[27]  Changfeng Tai,et al.  Simulation analysis of conduction block in unmyelinated axons induced by high-frequency biphasic electrical currents , 2005, IEEE Transactions on Biomedical Engineering.

[28]  E Eldred,et al.  Control of muscle contractile force through indirect high-frequency stimulation. , 1983, American journal of physical medicine.

[29]  Niloy Bhadra,et al.  High frequency electrical conduction block of the pudendal nerve , 2006, Journal of neural engineering.

[30]  S. Costa,et al.  The use of the rat isolated vagus nerve for functional measurements of the effect of drugs in vitro. , 2005, Journal of pharmacological and toxicological methods.