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The role of humic substances in drinking water in Kashin-Beck disease in China.

We conducted in vitro and in vivo assays in a selenium-deficient system to determine if organic matter (mainly fulvic acid; FA) is involved in a free radical mechanism of action for Kashin-Beck disease. Cartilage cell culture experiments indicated that the oxy or hydroxy functional groups in FA may...

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Detalles Bibliográficos
Autores principales: Peng, A, Wang, W H, Wang, C X, Wang, Z J, Rui, H F, Wang, W Z, Yang, Z W
Formato: Texto
Lenguaje:English
Publicado: 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1566521/
https://www.ncbi.nlm.nih.gov/pubmed/10090708
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author Peng, A
Wang, W H
Wang, C X
Wang, Z J
Rui, H F
Wang, W Z
Yang, Z W
author_facet Peng, A
Wang, W H
Wang, C X
Wang, Z J
Rui, H F
Wang, W Z
Yang, Z W
author_sort Peng, A
collection PubMed
description We conducted in vitro and in vivo assays in a selenium-deficient system to determine if organic matter (mainly fulvic acid; FA) is involved in a free radical mechanism of action for Kashin-Beck disease. Cartilage cell culture experiments indicated that the oxy or hydroxy functional groups in FA may interfere with the cell membrane and result in enhancement of lipid peroxidation. Experiments with rats demonstrated that toxicity from FA was reduced when the hydroxy group was blocked. Induction of lipid peroxidation by FA in liver and blood of rats was similar to that exhibited by acetyl phenyl hydrazine. FA accumulated in bone and cartilage, where selenium rarely concentrates. In addition, selenium supplementation in rats' drinking water inhibited the generation of oxy-free radicals in bone. We hypothesized that FA in drinking water is an etiological factor of Kashin-Beck disease and that the mechanism of action involves the oxy and hydroxy groups in FA for the generation of free radicals. Selenium was confirmed to be a preventive factor for Kashin-Beck disease.
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spelling pubmed-15665212006-09-19 The role of humic substances in drinking water in Kashin-Beck disease in China. Peng, A Wang, W H Wang, C X Wang, Z J Rui, H F Wang, W Z Yang, Z W Environ Health Perspect Research Article We conducted in vitro and in vivo assays in a selenium-deficient system to determine if organic matter (mainly fulvic acid; FA) is involved in a free radical mechanism of action for Kashin-Beck disease. Cartilage cell culture experiments indicated that the oxy or hydroxy functional groups in FA may interfere with the cell membrane and result in enhancement of lipid peroxidation. Experiments with rats demonstrated that toxicity from FA was reduced when the hydroxy group was blocked. Induction of lipid peroxidation by FA in liver and blood of rats was similar to that exhibited by acetyl phenyl hydrazine. FA accumulated in bone and cartilage, where selenium rarely concentrates. In addition, selenium supplementation in rats' drinking water inhibited the generation of oxy-free radicals in bone. We hypothesized that FA in drinking water is an etiological factor of Kashin-Beck disease and that the mechanism of action involves the oxy and hydroxy groups in FA for the generation of free radicals. Selenium was confirmed to be a preventive factor for Kashin-Beck disease. 1999-04 /pmc/articles/PMC1566521/ /pubmed/10090708 Text en
spellingShingle Research Article
Peng, A
Wang, W H
Wang, C X
Wang, Z J
Rui, H F
Wang, W Z
Yang, Z W
The role of humic substances in drinking water in Kashin-Beck disease in China.
title The role of humic substances in drinking water in Kashin-Beck disease in China.
title_full The role of humic substances in drinking water in Kashin-Beck disease in China.
title_fullStr The role of humic substances in drinking water in Kashin-Beck disease in China.
title_full_unstemmed The role of humic substances in drinking water in Kashin-Beck disease in China.
title_short The role of humic substances in drinking water in Kashin-Beck disease in China.
title_sort role of humic substances in drinking water in kashin-beck disease in china.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1566521/
https://www.ncbi.nlm.nih.gov/pubmed/10090708
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