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Effects of chronic arsenic exposure on hematopoietic function in adult mammalian liver
In these studies the effects of ingested arsenic (As(+5)) on hepatic heme biosynthetic capability and hemoprotein function in adult male rats were investigated. Animals exposed for 6 weeks to 0, 20, 40, or 85 ppm sodium arsenate in the drinking water suffered depression of hepatic δ-aminolevulinic a...
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Formato: | Texto |
Lenguaje: | English |
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1977
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1637394/ https://www.ncbi.nlm.nih.gov/pubmed/908300 |
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author | Woods, James S. Fowler, Bruce A. |
author_facet | Woods, James S. Fowler, Bruce A. |
author_sort | Woods, James S. |
collection | PubMed |
description | In these studies the effects of ingested arsenic (As(+5)) on hepatic heme biosynthetic capability and hemoprotein function in adult male rats were investigated. Animals exposed for 6 weeks to 0, 20, 40, or 85 ppm sodium arsenate in the drinking water suffered depression of hepatic δ-aminolevulinic acid (ALA) synthetase and heme synthetase (ferrochelatase) activities, with maximal decreases to 67 and 55% of control levels, respectively, at 85 ppm. Concomitantly, urinary uroporphyrin levels were elevated by as much as 12 times, and coproporphyrin by as much as 9 times, control values. The rate of incorporation of (3)H-ALA into mitochondrial and microsomal hemes was depressed by 40–50% at 20 ppm but was increased with regard to controls by as much as 150% at the higher treatment levels. A similar biphasic pattern was observed in regard to (14)C-leucine incorporation into cellular membranal proteins. In contrast, the levels of ALA dehydratase, uroporphyrinogen I synthetase, aminopyrine demethylase, and cytochrome P-450 were not significantly changed in As(+5)-treated rats. These results support the hypothesis that chronic, low level, arsenic exposure results in selective inhibition of mitochondrial-bound heme biosynthetic pathway enzymes (ALA synthetase and heme synthetase) resulting in a substantial increase in urinary porphyrins, uniquely characterized by a greater increase in uroporphyrin than coproporphyrin levels. These changes occur independent of, or prior to, alterations in hepatic hemoprotein-dependent functions and may thus serve in the clinical analysis of pretoxic exposure to arsenic compounds in human populations. |
format | Text |
id | pubmed-1637394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1977 |
record_format | MEDLINE/PubMed |
spelling | pubmed-16373942006-11-17 Effects of chronic arsenic exposure on hematopoietic function in adult mammalian liver Woods, James S. Fowler, Bruce A. Environ Health Perspect Articles In these studies the effects of ingested arsenic (As(+5)) on hepatic heme biosynthetic capability and hemoprotein function in adult male rats were investigated. Animals exposed for 6 weeks to 0, 20, 40, or 85 ppm sodium arsenate in the drinking water suffered depression of hepatic δ-aminolevulinic acid (ALA) synthetase and heme synthetase (ferrochelatase) activities, with maximal decreases to 67 and 55% of control levels, respectively, at 85 ppm. Concomitantly, urinary uroporphyrin levels were elevated by as much as 12 times, and coproporphyrin by as much as 9 times, control values. The rate of incorporation of (3)H-ALA into mitochondrial and microsomal hemes was depressed by 40–50% at 20 ppm but was increased with regard to controls by as much as 150% at the higher treatment levels. A similar biphasic pattern was observed in regard to (14)C-leucine incorporation into cellular membranal proteins. In contrast, the levels of ALA dehydratase, uroporphyrinogen I synthetase, aminopyrine demethylase, and cytochrome P-450 were not significantly changed in As(+5)-treated rats. These results support the hypothesis that chronic, low level, arsenic exposure results in selective inhibition of mitochondrial-bound heme biosynthetic pathway enzymes (ALA synthetase and heme synthetase) resulting in a substantial increase in urinary porphyrins, uniquely characterized by a greater increase in uroporphyrin than coproporphyrin levels. These changes occur independent of, or prior to, alterations in hepatic hemoprotein-dependent functions and may thus serve in the clinical analysis of pretoxic exposure to arsenic compounds in human populations. 1977-08 /pmc/articles/PMC1637394/ /pubmed/908300 Text en |
spellingShingle | Articles Woods, James S. Fowler, Bruce A. Effects of chronic arsenic exposure on hematopoietic function in adult mammalian liver |
title | Effects of chronic arsenic exposure on hematopoietic function in adult mammalian liver |
title_full | Effects of chronic arsenic exposure on hematopoietic function in adult mammalian liver |
title_fullStr | Effects of chronic arsenic exposure on hematopoietic function in adult mammalian liver |
title_full_unstemmed | Effects of chronic arsenic exposure on hematopoietic function in adult mammalian liver |
title_short | Effects of chronic arsenic exposure on hematopoietic function in adult mammalian liver |
title_sort | effects of chronic arsenic exposure on hematopoietic function in adult mammalian liver |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1637394/ https://www.ncbi.nlm.nih.gov/pubmed/908300 |
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