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Blood-brain barrier dysfunction in acute lead encephalopathy: a reappraisal.

Acute lead encephalopathy was induced in adult guinea pigs by administering daily oral doses of lead carbonate. During the development of the encephalopathy, the structural and functional integrity of the blood-brain barrier was evaluated with electron microscopy and tracer probes. Blood, cerebral g...

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Detalles Bibliográficos
Autores principales: Bouldin, T W, Mushak, P, O'Tuama, L A, Krigman, M R
Formato: Texto
Lenguaje:English
Publicado: 1975
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1475036/
https://www.ncbi.nlm.nih.gov/pubmed/1227864
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author Bouldin, T W
Mushak, P
O'Tuama, L A
Krigman, M R
author_facet Bouldin, T W
Mushak, P
O'Tuama, L A
Krigman, M R
author_sort Bouldin, T W
collection PubMed
description Acute lead encephalopathy was induced in adult guinea pigs by administering daily oral doses of lead carbonate. During the development of the encephalopathy, the structural and functional integrity of the blood-brain barrier was evaluated with electron microscopy and tracer probes. Blood, cerebral gray matter, liver, and kidney were analyzed for lead, calcium, and magnesium content. The animals regularly developed an encephalopathy after four doses of lead. There were no discernible pathomorphologic alterations in the cerebral capillaries or perivascular glial sheaths. Furthermore, no evidence of blood-brain barrier dysfunction was demonstrated with Evans blue-albumin complex or horseradish peroxidase. Blood-brain barrier permeability to radiolead was not increased in the intoxicated animals. During the development of the encephalopathy there was a progressive rise in the lead concentration in all tissues. Concurrently, there was a significant rise in brain calcium. These results suggest that the encephalopathic effects of lead may be mediated directly at the neuronal level.
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spelling pubmed-14750362006-06-09 Blood-brain barrier dysfunction in acute lead encephalopathy: a reappraisal. Bouldin, T W Mushak, P O'Tuama, L A Krigman, M R Environ Health Perspect Research Article Acute lead encephalopathy was induced in adult guinea pigs by administering daily oral doses of lead carbonate. During the development of the encephalopathy, the structural and functional integrity of the blood-brain barrier was evaluated with electron microscopy and tracer probes. Blood, cerebral gray matter, liver, and kidney were analyzed for lead, calcium, and magnesium content. The animals regularly developed an encephalopathy after four doses of lead. There were no discernible pathomorphologic alterations in the cerebral capillaries or perivascular glial sheaths. Furthermore, no evidence of blood-brain barrier dysfunction was demonstrated with Evans blue-albumin complex or horseradish peroxidase. Blood-brain barrier permeability to radiolead was not increased in the intoxicated animals. During the development of the encephalopathy there was a progressive rise in the lead concentration in all tissues. Concurrently, there was a significant rise in brain calcium. These results suggest that the encephalopathic effects of lead may be mediated directly at the neuronal level. 1975-12 /pmc/articles/PMC1475036/ /pubmed/1227864 Text en
spellingShingle Research Article
Bouldin, T W
Mushak, P
O'Tuama, L A
Krigman, M R
Blood-brain barrier dysfunction in acute lead encephalopathy: a reappraisal.
title Blood-brain barrier dysfunction in acute lead encephalopathy: a reappraisal.
title_full Blood-brain barrier dysfunction in acute lead encephalopathy: a reappraisal.
title_fullStr Blood-brain barrier dysfunction in acute lead encephalopathy: a reappraisal.
title_full_unstemmed Blood-brain barrier dysfunction in acute lead encephalopathy: a reappraisal.
title_short Blood-brain barrier dysfunction in acute lead encephalopathy: a reappraisal.
title_sort blood-brain barrier dysfunction in acute lead encephalopathy: a reappraisal.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1475036/
https://www.ncbi.nlm.nih.gov/pubmed/1227864
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