Dose-response study of the pathological effects of chronically applied direct current stimulation on the normal rat spinal cord.

Electrical stimulation of the mammalian central nervous system (CNS) can result in extensive destruction of tissue unless applied within specific stimulation parameters. Classically, unbalanced or monopolar currents have been avoided in order to minimize these harmful effects. However, direct current (DC) fields have recently been proposed for the treatment of spinal cord injury. Until now, no rigorous analysis has been made of the safety of these fields in the mammalian CNS. The purpose of this study was to determine the amount of chronically applied DC current that can be tolerated by the normal rodent spinal cord stimulated with metal disc electrodes. Thirty-five normal rats underwent implantation of DC stimulating devices and were allowed to recover for a period of 2 to 12 weeks. The stimulators delivered constant currents of 0 to 50 microA through two disc-shaped platinum/iridium electrodes positioned extradurally at the C-7 and T-3 levels. Following sacrifice of the animals, serial 8-microns cross sections of the spinal cord at the electrode sites were examined microscopically. Evidence of demyelination presumed due to the physical presence of the rostral electrode was seen in animals from most groups including control animals. Pathological changes directly attributable to the applied fields were seen with current as low as 3 microA. It was concluded that DC's of 3 microA or more are harmful to the mammalian CNS with this method of stimulation. In addition, the data suggest that the maximum current density tolerated by the rodent spinal cord is in the order of 75 microA/sq cm. These findings have important implications for the use of chronic DC stimulation in the mammalian CNS.

[1]  C. McCaig,et al.  The direction of growth of differentiating neurones and myoblasts from frog embryos in an applied electric field. , 1981, The Journal of physiology.

[2]  B. B. Lee,et al.  Deleterious effects of prolonged electrical excitation of striate cortex in macaques. , 1977, Brain, behavior and evolution.

[3]  A. Blight,et al.  Transected dorsal column axons within the guinea pig spinal cord regenerate in the presence of an applied electric field , 1986, The Journal of comparative neurology.

[4]  R. H. Clarke,et al.  THE STRUCTURE AND FUNCTIONS OF THE CEREBELLUM EXAMINED BY A NEW METHOD. , 1908 .

[5]  L. Hench,et al.  Cortical histopathology following stimulation with metallic and carbon electrodes. , 1977, Brain, behavior and evolution.

[6]  S. Geisser,et al.  On methods in the analysis of profile data , 1959 .

[7]  M. Cohen,et al.  Modification of retrograde degeneration in transected spinal axons of the lamprey by applied DC current , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[8]  A Sances,et al.  Measure of tissue resistivity in experimental electrical burns. , 1985, The Journal of trauma.

[9]  L. Jaffe,et al.  Neurites grow faster towards the cathode than the anode in a steady field. , 1979, The Journal of experimental zoology.

[10]  R B Borgens,et al.  Enhanced spinal cord regeneration in lamprey by applied electric fields. , 1981, Science.

[11]  D. McCreery,et al.  Histopathologic evaluation of prolonged intracortical electrical stimulation , 1986, Experimental Neurology.

[12]  S. Brummer,et al.  Electrical stimulation with Pt electrodes: Trace analysis for dissolved platinum and other dissolved electrochemical products. , 1977, Brain, behavior and evolution.

[13]  J. Doppman,et al.  Acute occlusion of the posterior spinal vein. Experimental study in monkeys. , 1979, Journal of neurosurgery.

[14]  L. Tveten Spinal Cord Vascularity , 1976, Acta radiologica: diagnosis.

[15]  H. W. Beams,et al.  In vitro control of growing chick nerve fibers by applied electric currents. , 1946, Journal of cellular and comparative physiology.

[16]  M. Poo,et al.  Orientation of neurite growth by extracellular electric fields , 1982, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[17]  K. R. Robinson,et al.  The distribution of free calcium in transected spinal axons and its modulation by applied electrical fields , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[18]  Michael G. Fehlings,et al.  The effect of direct current field polarity on recovery after acute experimental spinal cord injury , 1992, Brain Research.

[19]  L A Bullara,et al.  Electrical stimulation of the brain. III. The neural damage model. , 1975, Surgical neurology.

[20]  M. Fehlings,et al.  The effect of direct-current field on recovery from experimental spinal cord injury. , 1988, Journal of neurosurgery.

[21]  J. R. Hughes,et al.  Brief, noninjurious electric waveform for stimulation of the brain. , 1955, Science.

[22]  D. McCreery,et al.  Morphologic changes after prolonged electrical stimulation of the cat's cortex at defined charge densities , 1983, Experimental Neurology.

[23]  S. Finkelstein,et al.  Naloxone and experimental spinal cord injury: Part 1. High dose administration in a static load compression model. , 1986, Neurosurgery.

[24]  C H Tator,et al.  Review of the secondary injury theory of acute spinal cord trauma with emphasis on vascular mechanisms. , 1991, Journal of neurosurgery.

[25]  C. McCaig Dynamic aspects of amphibian neurite growth and the effects of an applied electric field. , 1986, The Journal of physiology.

[26]  Charles Tator,et al.  Recovery of spinal cord function induced by direct current stimulation of the injured rat spinal cord. , 1987, Neurosurgery.

[27]  J. Weaver ELECTROPORATION: A NEW PHENOMENON TO CONSIDER IN MEDICAL TECHNOLOGY , 1990 .

[28]  R B Borgens,et al.  Behavioral recovery induced by applied electric fields after spinal cord hemisection in guinea pig. , 1987, Science.

[29]  C H Tator,et al.  Objective clinical assessment of motor function after experimental spinal cord injury in the rat. , 1977, Journal of neurosurgery.

[30]  Raphael C. Lee,et al.  Electrical Injury Mechanisms: Electrical Breakdown of Cell Membranes , 1987, Plastic and reconstructive surgery.

[31]  S. B. Brummer,et al.  Electrochemical Considerations for Safe Electrical Stimulation of the Nervous System with Platinum Electrodes , 1977, IEEE Transactions on Biomedical Engineering.

[32]  A. Blight,et al.  Functional recovery after spinal cord hemisection in guinea pigs: The effects of applied electric fields , 1990, The Journal of comparative neurology.

[33]  D. McCreery,et al.  Histological evaluation of neural damage from electrical stimulation: considerations for the selection of parameters for clinical application. , 1981, Neurosurgery.

[34]  T. Yuen,et al.  NEUROPATHOLOGICAL EFFECTS OF INTRACEREBRAL PLATINUM SALT INJECTIONS , 1977, Journal of neuropathology and experimental neurology.

[35]  S. Finkelstein,et al.  Naloxone and experimental spinal cord injury: Part 2. Megadose treatment in a dynamic load injury model. , 1986, Neurosurgery.

[36]  D. McCreery,et al.  Changes in extracellular potassium and calcium concentration and neural activity during prolonged electrical stimulation of the cat cerebral cortex at defined charge densities , 1983, Experimental Neurology.

[37]  B. Sisken,et al.  The effects of minute direct electrical currents on cultured chick embryo trigeminal ganglia. , 1975, Journal of embryology and experimental morphology.

[38]  M. Zanakis,et al.  Short term efficacy of applied electric fields in the repair of the damaged rodent spinal cord: behavioral and morphological results. , 1988, Neurosurgery.