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Effect of Azide and Ca Ion on the Reversible Changes of Protein Configuration in Stimulated Nerves

Working with sciatic nerves from the South American frog Calyptocephalella gayi we have been able to substantiate the finding of Ungar et al., that nerve proteins undergo a reversible denaturation concomitant with a train of nerve impulses. We also showed that 0.3 mM sodium azide is capable of impai...

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Detalles Bibliográficos
Autores principales: Luxoro, M., Rojas, E., Wittig, E.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1963
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2195302/
https://www.ncbi.nlm.nih.gov/pubmed/13931864
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author Luxoro, M.
Rojas, E.
Wittig, E.
author_facet Luxoro, M.
Rojas, E.
Wittig, E.
author_sort Luxoro, M.
collection PubMed
description Working with sciatic nerves from the South American frog Calyptocephalella gayi we have been able to substantiate the finding of Ungar et al., that nerve proteins undergo a reversible denaturation concomitant with a train of nerve impulses. We also showed that 0.3 mM sodium azide is capable of impairing the reversibility of those changes. Furthermore, 10 meq/liter of calcium ion applied to extracts of resting nerves induce configurational rearrangements in the proteins similar to those produced during stimulation. We also proved that nerves previously kept in low calcium Ringer's solution do not show configurational changes upon stimulation. A tentative interpretation of the results described is that the configurational changes are a consequence of the extra influx of calcium ion due to nerve impulse propagation.
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spelling pubmed-21953022008-04-23 Effect of Azide and Ca Ion on the Reversible Changes of Protein Configuration in Stimulated Nerves Luxoro, M. Rojas, E. Wittig, E. J Gen Physiol Article Working with sciatic nerves from the South American frog Calyptocephalella gayi we have been able to substantiate the finding of Ungar et al., that nerve proteins undergo a reversible denaturation concomitant with a train of nerve impulses. We also showed that 0.3 mM sodium azide is capable of impairing the reversibility of those changes. Furthermore, 10 meq/liter of calcium ion applied to extracts of resting nerves induce configurational rearrangements in the proteins similar to those produced during stimulation. We also proved that nerves previously kept in low calcium Ringer's solution do not show configurational changes upon stimulation. A tentative interpretation of the results described is that the configurational changes are a consequence of the extra influx of calcium ion due to nerve impulse propagation. The Rockefeller University Press 1963-05-01 /pmc/articles/PMC2195302/ /pubmed/13931864 Text en Copyright © Copyright, 1963, by The Rockefeller Institute Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Luxoro, M.
Rojas, E.
Wittig, E.
Effect of Azide and Ca Ion on the Reversible Changes of Protein Configuration in Stimulated Nerves
title Effect of Azide and Ca Ion on the Reversible Changes of Protein Configuration in Stimulated Nerves
title_full Effect of Azide and Ca Ion on the Reversible Changes of Protein Configuration in Stimulated Nerves
title_fullStr Effect of Azide and Ca Ion on the Reversible Changes of Protein Configuration in Stimulated Nerves
title_full_unstemmed Effect of Azide and Ca Ion on the Reversible Changes of Protein Configuration in Stimulated Nerves
title_short Effect of Azide and Ca Ion on the Reversible Changes of Protein Configuration in Stimulated Nerves
title_sort effect of azide and ca ion on the reversible changes of protein configuration in stimulated nerves
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2195302/
https://www.ncbi.nlm.nih.gov/pubmed/13931864
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