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Comparison between electrophysiologic and morphologic changes in lead induced peripheral neuropathy in rats.

Compound nerve action potential (CNAP) of the mixed peripheral nerve is composed of A alpha beta, A delta, and C potentials. All components of CNAPs in the sciatic nerve were recorded by stimulating the tibial nerve of both control and lead-poisoned rats. Marked decrease of nerve conduction velocity...

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Detalles Bibliográficos
Autores principales: Hwang, Y. M., Sunwoo, I. N., Chung, I. H., Jung, B.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3053701/
https://www.ncbi.nlm.nih.gov/pubmed/2561732
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author Hwang, Y. M.
Sunwoo, I. N.
Chung, I. H.
Jung, B.
author_facet Hwang, Y. M.
Sunwoo, I. N.
Chung, I. H.
Jung, B.
author_sort Hwang, Y. M.
collection PubMed
description Compound nerve action potential (CNAP) of the mixed peripheral nerve is composed of A alpha beta, A delta, and C potentials. All components of CNAPs in the sciatic nerve were recorded by stimulating the tibial nerve of both control and lead-poisoned rats. Marked decrease of nerve conduction velocity and prolonged duration were found in A alpha beta and A delta fibers especially in large myelinated A alpha beta fibers. The amplitude decreased in A alpha beta potential, but the area did not change. In C potential produced by activation of unmyelinated fibers, nerve conduction velocity slightly decreased, but the amplitude and area did not significantly change. Pathologic correlates revealed prominent segmental demyelination with significant decrease of large myelinated fiber densities. Minimal axonal degeneration of unmyelinated fibers was present. We can conclude that electrophysiologic changes in the lead-poisoned rats correlate with pathologic changes in them.
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spelling pubmed-30537012011-03-16 Comparison between electrophysiologic and morphologic changes in lead induced peripheral neuropathy in rats. Hwang, Y. M. Sunwoo, I. N. Chung, I. H. Jung, B. J Korean Med Sci Research Article Compound nerve action potential (CNAP) of the mixed peripheral nerve is composed of A alpha beta, A delta, and C potentials. All components of CNAPs in the sciatic nerve were recorded by stimulating the tibial nerve of both control and lead-poisoned rats. Marked decrease of nerve conduction velocity and prolonged duration were found in A alpha beta and A delta fibers especially in large myelinated A alpha beta fibers. The amplitude decreased in A alpha beta potential, but the area did not change. In C potential produced by activation of unmyelinated fibers, nerve conduction velocity slightly decreased, but the amplitude and area did not significantly change. Pathologic correlates revealed prominent segmental demyelination with significant decrease of large myelinated fiber densities. Minimal axonal degeneration of unmyelinated fibers was present. We can conclude that electrophysiologic changes in the lead-poisoned rats correlate with pathologic changes in them. Korean Academy of Medical Sciences 1989-12 /pmc/articles/PMC3053701/ /pubmed/2561732 Text en
spellingShingle Research Article
Hwang, Y. M.
Sunwoo, I. N.
Chung, I. H.
Jung, B.
Comparison between electrophysiologic and morphologic changes in lead induced peripheral neuropathy in rats.
title Comparison between electrophysiologic and morphologic changes in lead induced peripheral neuropathy in rats.
title_full Comparison between electrophysiologic and morphologic changes in lead induced peripheral neuropathy in rats.
title_fullStr Comparison between electrophysiologic and morphologic changes in lead induced peripheral neuropathy in rats.
title_full_unstemmed Comparison between electrophysiologic and morphologic changes in lead induced peripheral neuropathy in rats.
title_short Comparison between electrophysiologic and morphologic changes in lead induced peripheral neuropathy in rats.
title_sort comparison between electrophysiologic and morphologic changes in lead induced peripheral neuropathy in rats.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3053701/
https://www.ncbi.nlm.nih.gov/pubmed/2561732
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