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THE METABOLISM OF THE CENTRAL NERVOUS SYSTEM IN EXPERIMENTAL POLIOMYELITIS

1. During paralysis, the brain of the mouse infected with poliomyelitis virus shows on test after mincing a decrease in anaerobic glycolysis with no significant change in oxygen utilization. The decrease in anaerobic glycolysis varies from 5 per cent to 50 per cent. 2. Sodium fluoride produces a gre...

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Detalles Bibliográficos
Autores principales: Racker, E., Kabat, Herman
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1942
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2135281/
https://www.ncbi.nlm.nih.gov/pubmed/19871259
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author Racker, E.
Kabat, Herman
author_facet Racker, E.
Kabat, Herman
author_sort Racker, E.
collection PubMed
description 1. During paralysis, the brain of the mouse infected with poliomyelitis virus shows on test after mincing a decrease in anaerobic glycolysis with no significant change in oxygen utilization. The decrease in anaerobic glycolysis varies from 5 per cent to 50 per cent. 2. Sodium fluoride produces a greater inhibition of anaerobic glycolysis in normal than in poliomyelitic brain. 3. Dehydrogenase activity is higher for poliomyelitis-infected brain without added substrate. This difference from normal disappears when substrates are added. 4. The ratio of See PDF for Equation for the sliced motor cortex is higher than for sliced visual cortex of the dog and cat. 5. The oxygen consumption of the anterior horn of the sliced spinal cord of dog and cat is much less than that of the cerebral cortex. 6. The findings are in keeping with the view that, at a certain stage of the infection, the nerve cells may be reversibly injured but not yet destroyed by the virus.
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spelling pubmed-21352812008-04-18 THE METABOLISM OF THE CENTRAL NERVOUS SYSTEM IN EXPERIMENTAL POLIOMYELITIS Racker, E. Kabat, Herman J Exp Med Article 1. During paralysis, the brain of the mouse infected with poliomyelitis virus shows on test after mincing a decrease in anaerobic glycolysis with no significant change in oxygen utilization. The decrease in anaerobic glycolysis varies from 5 per cent to 50 per cent. 2. Sodium fluoride produces a greater inhibition of anaerobic glycolysis in normal than in poliomyelitic brain. 3. Dehydrogenase activity is higher for poliomyelitis-infected brain without added substrate. This difference from normal disappears when substrates are added. 4. The ratio of See PDF for Equation for the sliced motor cortex is higher than for sliced visual cortex of the dog and cat. 5. The oxygen consumption of the anterior horn of the sliced spinal cord of dog and cat is much less than that of the cerebral cortex. 6. The findings are in keeping with the view that, at a certain stage of the infection, the nerve cells may be reversibly injured but not yet destroyed by the virus. The Rockefeller University Press 1942-12-01 /pmc/articles/PMC2135281/ /pubmed/19871259 Text en Copyright © Copyright, 1942, by The Rockefeller Institute for Medical Research New York 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
Racker, E.
Kabat, Herman
THE METABOLISM OF THE CENTRAL NERVOUS SYSTEM IN EXPERIMENTAL POLIOMYELITIS
title THE METABOLISM OF THE CENTRAL NERVOUS SYSTEM IN EXPERIMENTAL POLIOMYELITIS
title_full THE METABOLISM OF THE CENTRAL NERVOUS SYSTEM IN EXPERIMENTAL POLIOMYELITIS
title_fullStr THE METABOLISM OF THE CENTRAL NERVOUS SYSTEM IN EXPERIMENTAL POLIOMYELITIS
title_full_unstemmed THE METABOLISM OF THE CENTRAL NERVOUS SYSTEM IN EXPERIMENTAL POLIOMYELITIS
title_short THE METABOLISM OF THE CENTRAL NERVOUS SYSTEM IN EXPERIMENTAL POLIOMYELITIS
title_sort metabolism of the central nervous system in experimental poliomyelitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2135281/
https://www.ncbi.nlm.nih.gov/pubmed/19871259
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