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THE BRAIN LESION OF GOLDTHIOGLUCOSE OBESITY

The development of hypothalamic lesions due to goldthioglucose are described. The initial extensive necrotic lesion occurs in close to 100 per cent of animals injected with LD (50). Within 2 weeks the necrotic material has been removed and a narrow scar results. After a lapse of several months, the...

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Detalles Bibliográficos
Autores principales: Brecher, G., Laqueur, G. L., Cronkite, E. P., Edelman, P. M., Schwartz, I. L.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1965
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137955/
https://www.ncbi.nlm.nih.gov/pubmed/14270240
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author Brecher, G.
Laqueur, G. L.
Cronkite, E. P.
Edelman, P. M.
Schwartz, I. L.
author_facet Brecher, G.
Laqueur, G. L.
Cronkite, E. P.
Edelman, P. M.
Schwartz, I. L.
author_sort Brecher, G.
collection PubMed
description The development of hypothalamic lesions due to goldthioglucose are described. The initial extensive necrotic lesion occurs in close to 100 per cent of animals injected with LD (50). Within 2 weeks the necrotic material has been removed and a narrow scar results. After a lapse of several months, the scar is often difficult to visualize, especially in animals that have not developed obesity. The ventromedial nucleus is not the center of the lesion. The nucleus is preserved in some instances, and partially or completely destroyed in others, depending on the extent of the lesion. The more prominent scar in the obese animals correlates with the larger initial lesion necessary for the complete bilateral destruction of the ventromedial nucleus which is known to be a prerequisite for the development of hypothalamic obesity. Thus, contrary to earlier suggestions, goldthioglucose does not localize specifically in the cells of the ventromedial nucleus.
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spelling pubmed-21379552008-04-17 THE BRAIN LESION OF GOLDTHIOGLUCOSE OBESITY Brecher, G. Laqueur, G. L. Cronkite, E. P. Edelman, P. M. Schwartz, I. L. J Exp Med Article The development of hypothalamic lesions due to goldthioglucose are described. The initial extensive necrotic lesion occurs in close to 100 per cent of animals injected with LD (50). Within 2 weeks the necrotic material has been removed and a narrow scar results. After a lapse of several months, the scar is often difficult to visualize, especially in animals that have not developed obesity. The ventromedial nucleus is not the center of the lesion. The nucleus is preserved in some instances, and partially or completely destroyed in others, depending on the extent of the lesion. The more prominent scar in the obese animals correlates with the larger initial lesion necessary for the complete bilateral destruction of the ventromedial nucleus which is known to be a prerequisite for the development of hypothalamic obesity. Thus, contrary to earlier suggestions, goldthioglucose does not localize specifically in the cells of the ventromedial nucleus. The Rockefeller University Press 1965-02-28 /pmc/articles/PMC2137955/ /pubmed/14270240 Text en Copyright © 1965 by The Rockefeller Institute 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
Brecher, G.
Laqueur, G. L.
Cronkite, E. P.
Edelman, P. M.
Schwartz, I. L.
THE BRAIN LESION OF GOLDTHIOGLUCOSE OBESITY
title THE BRAIN LESION OF GOLDTHIOGLUCOSE OBESITY
title_full THE BRAIN LESION OF GOLDTHIOGLUCOSE OBESITY
title_fullStr THE BRAIN LESION OF GOLDTHIOGLUCOSE OBESITY
title_full_unstemmed THE BRAIN LESION OF GOLDTHIOGLUCOSE OBESITY
title_short THE BRAIN LESION OF GOLDTHIOGLUCOSE OBESITY
title_sort brain lesion of goldthioglucose obesity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137955/
https://www.ncbi.nlm.nih.gov/pubmed/14270240
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