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Quantifying Demyelination in NK venom treated nerve using its electric circuit model

Reduction of myelin in peripheral nerve causes critical demyelinating diseases such as chronic inflammatory demyelinating polyneuropathy, Guillain-Barre syndrome, etc. Clinical monitoring of these diseases requires rapid and non-invasive quantification of demyelination. Here we have developed formul...

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Autores principales: Das, H. K., Das, D., Doley, R., Sahu, P. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773768/
https://www.ncbi.nlm.nih.gov/pubmed/26932543
http://dx.doi.org/10.1038/srep22385
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author Das, H. K.
Das, D.
Doley, R.
Sahu, P. P.
author_facet Das, H. K.
Das, D.
Doley, R.
Sahu, P. P.
author_sort Das, H. K.
collection PubMed
description Reduction of myelin in peripheral nerve causes critical demyelinating diseases such as chronic inflammatory demyelinating polyneuropathy, Guillain-Barre syndrome, etc. Clinical monitoring of these diseases requires rapid and non-invasive quantification of demyelination. Here we have developed formulation of nerve conduction velocity (NCV) in terms of demyelination considering electric circuit model of a nerve having bundle of axons for its quantification from NCV measurements. This approach has been validated and demonstrated with toad nerve model treated with crude Naja kaouthia (NK) venom and also shows the effect of Phospholipase A(2) and three finger neurotoxin from NK-venom on peripheral nerve. This opens future scope for non-invasive clinical measurement of demyelination.
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spelling pubmed-47737682016-03-07 Quantifying Demyelination in NK venom treated nerve using its electric circuit model Das, H. K. Das, D. Doley, R. Sahu, P. P. Sci Rep Article Reduction of myelin in peripheral nerve causes critical demyelinating diseases such as chronic inflammatory demyelinating polyneuropathy, Guillain-Barre syndrome, etc. Clinical monitoring of these diseases requires rapid and non-invasive quantification of demyelination. Here we have developed formulation of nerve conduction velocity (NCV) in terms of demyelination considering electric circuit model of a nerve having bundle of axons for its quantification from NCV measurements. This approach has been validated and demonstrated with toad nerve model treated with crude Naja kaouthia (NK) venom and also shows the effect of Phospholipase A(2) and three finger neurotoxin from NK-venom on peripheral nerve. This opens future scope for non-invasive clinical measurement of demyelination. Nature Publishing Group 2016-03-02 /pmc/articles/PMC4773768/ /pubmed/26932543 http://dx.doi.org/10.1038/srep22385 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Das, H. K.
Das, D.
Doley, R.
Sahu, P. P.
Quantifying Demyelination in NK venom treated nerve using its electric circuit model
title Quantifying Demyelination in NK venom treated nerve using its electric circuit model
title_full Quantifying Demyelination in NK venom treated nerve using its electric circuit model
title_fullStr Quantifying Demyelination in NK venom treated nerve using its electric circuit model
title_full_unstemmed Quantifying Demyelination in NK venom treated nerve using its electric circuit model
title_short Quantifying Demyelination in NK venom treated nerve using its electric circuit model
title_sort quantifying demyelination in nk venom treated nerve using its electric circuit model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773768/
https://www.ncbi.nlm.nih.gov/pubmed/26932543
http://dx.doi.org/10.1038/srep22385
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