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Hypohaptoglobinemia associated with familial epilepsy

In select kindreds afflicted with familial idiopathic epilepsy, most individuals suffering seizures also have low levels of the plasma hemoglobin-binding protein, haptoglobin. This hypohaptoglobinemia may be causally associated with a tendency to develop epilepsy. Our experimental results indicate t...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1985
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189065/
https://www.ncbi.nlm.nih.gov/pubmed/3981086
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description In select kindreds afflicted with familial idiopathic epilepsy, most individuals suffering seizures also have low levels of the plasma hemoglobin-binding protein, haptoglobin. This hypohaptoglobinemia may be causally associated with a tendency to develop epilepsy. Our experimental results indicate that artificially-induced hypohaptoglobinemia in mice causes retarded clearance of free hemoglobin from the central nervous system, and that such free hemoglobin may engender the peroxidation of brain lipids. We hypothesize that hypohaptoglobinemia, either inherited, or acquired via traumatic processes, may prevent efficient clearance of interstitial hemoglobin from the central nervous system, thereby predisposing these people to encephalic inflammation and the appearance of seizure disorders.
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spelling pubmed-21890652008-04-17 Hypohaptoglobinemia associated with familial epilepsy J Exp Med Articles In select kindreds afflicted with familial idiopathic epilepsy, most individuals suffering seizures also have low levels of the plasma hemoglobin-binding protein, haptoglobin. This hypohaptoglobinemia may be causally associated with a tendency to develop epilepsy. Our experimental results indicate that artificially-induced hypohaptoglobinemia in mice causes retarded clearance of free hemoglobin from the central nervous system, and that such free hemoglobin may engender the peroxidation of brain lipids. We hypothesize that hypohaptoglobinemia, either inherited, or acquired via traumatic processes, may prevent efficient clearance of interstitial hemoglobin from the central nervous system, thereby predisposing these people to encephalic inflammation and the appearance of seizure disorders. The Rockefeller University Press 1985-04-01 /pmc/articles/PMC2189065/ /pubmed/3981086 Text en 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 Articles
Hypohaptoglobinemia associated with familial epilepsy
title Hypohaptoglobinemia associated with familial epilepsy
title_full Hypohaptoglobinemia associated with familial epilepsy
title_fullStr Hypohaptoglobinemia associated with familial epilepsy
title_full_unstemmed Hypohaptoglobinemia associated with familial epilepsy
title_short Hypohaptoglobinemia associated with familial epilepsy
title_sort hypohaptoglobinemia associated with familial epilepsy
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189065/
https://www.ncbi.nlm.nih.gov/pubmed/3981086