Large naturally-produced electric currents and voltage traverse damaged mammalian spinal cord

<p>Abstract</p> <p>Background</p> <p>Immediately after damage to the nervous system, a cascade of physical, physiological, and anatomical events lead to the collapse of neuronal function and often death. This progression of injury processes is called "secondary inj...

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Main Authors: Borgens Richard B, Porterfield David M, ul Haque Aeraj, Liu-Snyder Peishan, Zuberi Mahvash
Format: Article
Language:English
Published: BMC 2008-12-01
Series:Journal of Biological Engineering
Online Access:http://www.jbioleng.org/content/2/1/17
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spelling doaj-6b39a271a5e74e45bba86f45ef24687b2020-11-24T21:44:38ZengBMCJournal of Biological Engineering1754-16112008-12-01211710.1186/1754-1611-2-17Large naturally-produced electric currents and voltage traverse damaged mammalian spinal cordBorgens Richard BPorterfield David Mul Haque AerajLiu-Snyder PeishanZuberi Mahvash<p>Abstract</p> <p>Background</p> <p>Immediately after damage to the nervous system, a cascade of physical, physiological, and anatomical events lead to the collapse of neuronal function and often death. This progression of injury processes is called "secondary injury." In the spinal cord and brain, this loss in function and anatomy is largely irreversible, except at the earliest stages. We investigated the most ignored and earliest component of secondary injury. Large bioelectric currents immediately enter damaged cells and tissues of guinea pig spinal cords. The driving force behind these currents is the potential difference of adjacent intact cell membranes. For perhaps days, it is the biophysical events caused by trauma that predominate in the early biology of neurotrauma.</p> <p>Results</p> <p>An enormous (≤ mA/cm<sup>2</sup>) bioelectric current transverses the site of injury to the mammalian spinal cord. This endogenous current declines with time and with distance from the local site of injury but eventually maintains a much lower but stable value (< 50 μA/cm<sup>2</sup>).</p> <p>The calcium component of this net current, about 2.0 pmoles/cm<sup>2</sup>/sec entering the site of damage for a minimum of an hour, is significant. Curiously, injury currents entering the ventral portion of the spinal cord may be as high as 10 fold greater than those entering the dorsal surface, and there is little difference in the magnitude of currents associated with crush injuries compared to cord transection. Physiological measurements were performed with non-invasive sensors: one and two-dimensional extracellular vibrating electrodes in real time. The calcium measurement was performed with a self-referencing calcium selective electrode.</p> <p>Conclusion</p> <p>The enormous bioelectric current, carried in part by free calcium, is the major initiator of secondary injury processes and causes significant damage after breach of the membranes of vulnerable cells adjacent to the injury site. The large intra-cellular voltages, polarized along the length of axons in particular, are believed to be associated with zones of organelle death, distortion, and asymmetry observed in acutely injured nerve fibers. These data enlarge our understanding of secondary mechanisms and provide new ways to consider interfering with this catabolic and progressive loss of tissue.</p> http://www.jbioleng.org/content/2/1/17
collection DOAJ
language English
format Article
sources DOAJ
author Borgens Richard B
Porterfield David M
ul Haque Aeraj
Liu-Snyder Peishan
Zuberi Mahvash
spellingShingle Borgens Richard B
Porterfield David M
ul Haque Aeraj
Liu-Snyder Peishan
Zuberi Mahvash
Large naturally-produced electric currents and voltage traverse damaged mammalian spinal cord
Journal of Biological Engineering
author_facet Borgens Richard B
Porterfield David M
ul Haque Aeraj
Liu-Snyder Peishan
Zuberi Mahvash
author_sort Borgens Richard B
title Large naturally-produced electric currents and voltage traverse damaged mammalian spinal cord
title_short Large naturally-produced electric currents and voltage traverse damaged mammalian spinal cord
title_full Large naturally-produced electric currents and voltage traverse damaged mammalian spinal cord
title_fullStr Large naturally-produced electric currents and voltage traverse damaged mammalian spinal cord
title_full_unstemmed Large naturally-produced electric currents and voltage traverse damaged mammalian spinal cord
title_sort large naturally-produced electric currents and voltage traverse damaged mammalian spinal cord
publisher BMC
series Journal of Biological Engineering
issn 1754-1611
publishDate 2008-12-01
description <p>Abstract</p> <p>Background</p> <p>Immediately after damage to the nervous system, a cascade of physical, physiological, and anatomical events lead to the collapse of neuronal function and often death. This progression of injury processes is called "secondary injury." In the spinal cord and brain, this loss in function and anatomy is largely irreversible, except at the earliest stages. We investigated the most ignored and earliest component of secondary injury. Large bioelectric currents immediately enter damaged cells and tissues of guinea pig spinal cords. The driving force behind these currents is the potential difference of adjacent intact cell membranes. For perhaps days, it is the biophysical events caused by trauma that predominate in the early biology of neurotrauma.</p> <p>Results</p> <p>An enormous (≤ mA/cm<sup>2</sup>) bioelectric current transverses the site of injury to the mammalian spinal cord. This endogenous current declines with time and with distance from the local site of injury but eventually maintains a much lower but stable value (< 50 μA/cm<sup>2</sup>).</p> <p>The calcium component of this net current, about 2.0 pmoles/cm<sup>2</sup>/sec entering the site of damage for a minimum of an hour, is significant. Curiously, injury currents entering the ventral portion of the spinal cord may be as high as 10 fold greater than those entering the dorsal surface, and there is little difference in the magnitude of currents associated with crush injuries compared to cord transection. Physiological measurements were performed with non-invasive sensors: one and two-dimensional extracellular vibrating electrodes in real time. The calcium measurement was performed with a self-referencing calcium selective electrode.</p> <p>Conclusion</p> <p>The enormous bioelectric current, carried in part by free calcium, is the major initiator of secondary injury processes and causes significant damage after breach of the membranes of vulnerable cells adjacent to the injury site. The large intra-cellular voltages, polarized along the length of axons in particular, are believed to be associated with zones of organelle death, distortion, and asymmetry observed in acutely injured nerve fibers. These data enlarge our understanding of secondary mechanisms and provide new ways to consider interfering with this catabolic and progressive loss of tissue.</p>
url http://www.jbioleng.org/content/2/1/17
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