A review on environmental factors regulating arsenic methylation in humans

Subjects exposed to arsenic show significant inter-individual variation in urinary patterns of arsenic metabolites but insignificant day-to-day intra-individual variation. The inter-individual variation in arsenic methylation can be partly responsible for the variation in susceptibility to arsenic t...

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Published inToxicology and applied pharmacology Vol. 235; no. 3; pp. 338 - 350
Main Author Tseng, Chin-Hsiao
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Inc 15.03.2009
Elsevier
Subjects
Online AccessGet full text
ISSN0041-008X
1096-0333
1096-0333
DOI10.1016/j.taap.2008.12.016

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Abstract Subjects exposed to arsenic show significant inter-individual variation in urinary patterns of arsenic metabolites but insignificant day-to-day intra-individual variation. The inter-individual variation in arsenic methylation can be partly responsible for the variation in susceptibility to arsenic toxicity. Wide inter-ethnic variation and family correlation in urinary arsenic profile suggest a genetic effect on arsenic metabolism. In this paper the environmental factors affecting arsenic metabolism are reviewed. Methylation capacity might reduce with increasing dosage of arsenic exposure. Furthermore, women, especially at pregnancy, have better methylation capacity than their men counterparts, probably due to the effect of estrogen. Children might have better methylation capacity than adults and age shows inconsistent relevance in adults. Smoking and alcohol consumption might be associated with a poorer methylation capacity. Nutritional status is important in the methylation capacity and folate may facilitate the methylation and excretion of arsenic. Besides, general health conditions and medications might influence the arsenic methylation capacity; and technical problems can cause biased estimates. The consumption of seafood, seaweed, rice and other food with high arsenic contents and the extent of cooking and arsenic-containing water used in food preparation may also interfere with the presentation of the urinary arsenic profile. Future studies are necessary to clarify the effects of the various arsenic metabolites including the trivalent methylated forms on the development of arsenic-induced human diseases with the consideration of the effects of confounding factors and the interactions with other effect modifiers.
AbstractList Subjects exposed to arsenic show significant inter-individual variation in urinary patterns of arsenic metabolites but insignificant day-to-day intra-individual variation. The inter-individual variation in arsenic methylation can be partly responsible for the variation in susceptibility to arsenic toxicity. Wide inter-ethnic variation and family correlation in urinary arsenic profile suggest a genetic effect on arsenic metabolism. In this paper the environmental factors affecting arsenic metabolism are reviewed. Methylation capacity might reduce with increasing dosage of arsenic exposure. Furthermore, women, especially at pregnancy, have better methylation capacity than their men counterparts, probably due to the effect of estrogen. Children might have better methylation capacity than adults and age shows inconsistent relevance in adults. Smoking and alcohol consumption might be associated with a poorer methylation capacity. Nutritional status is important in the methylation capacity and folate may facilitate the methylation and excretion of arsenic. Besides, general health conditions and medications might influence the arsenic methylation capacity; and technical problems can cause biased estimates. The consumption of seafood, seaweed, rice and other food with high arsenic contents and the extent of cooking and arsenic-containing water used in food preparation may also interfere with the presentation of the urinary arsenic profile. Future studies are necessary to clarify the effects of the various arsenic metabolites including the trivalent methylated forms on the development of arsenic-induced human diseases with the consideration of the effects of confounding factors and the interactions with other effect modifiers.
Subjects exposed to arsenic show significant inter-individual variation in urinary patterns of arsenic metabolites but insignificant day-to-day intra-individual variation. The inter-individual variation in arsenic methylation can be partly responsible for the variation in susceptibility to arsenic toxicity. Wide inter-ethnic variation and family correlation in urinary arsenic profile suggest a genetic effect on arsenic metabolism. In this paper the environmental factors affecting arsenic metabolism are reviewed. Methylation capacity might reduce with increasing dosage of arsenic exposure. Furthermore, women, especially at pregnancy, have better methylation capacity than their men counterparts, probably due to the effect of estrogen. Children might have better methylation capacity than adults and age shows inconsistent relevance in adults. Smoking and alcohol consumption might be associated with a poorer methylation capacity. Nutritional status is important in the methylation capacity and folate may facilitate the methylation and excretion of arsenic. Besides, general health conditions and medications might influence the arsenic methylation capacity; and technical problems can cause biased estimates. The consumption of seafood, seaweed, rice and other food with high arsenic contents and the extent of cooking and arsenic-containing water used in food preparation may also interfere with the presentation of the urinary arsenic profile. Future studies are necessary to clarify the effects of the various arsenic metabolites including the trivalent methylated forms on the development of arsenic-induced human diseases with the consideration of the effects of confounding factors and the interactions with other effect modifiers.Subjects exposed to arsenic show significant inter-individual variation in urinary patterns of arsenic metabolites but insignificant day-to-day intra-individual variation. The inter-individual variation in arsenic methylation can be partly responsible for the variation in susceptibility to arsenic toxicity. Wide inter-ethnic variation and family correlation in urinary arsenic profile suggest a genetic effect on arsenic metabolism. In this paper the environmental factors affecting arsenic metabolism are reviewed. Methylation capacity might reduce with increasing dosage of arsenic exposure. Furthermore, women, especially at pregnancy, have better methylation capacity than their men counterparts, probably due to the effect of estrogen. Children might have better methylation capacity than adults and age shows inconsistent relevance in adults. Smoking and alcohol consumption might be associated with a poorer methylation capacity. Nutritional status is important in the methylation capacity and folate may facilitate the methylation and excretion of arsenic. Besides, general health conditions and medications might influence the arsenic methylation capacity; and technical problems can cause biased estimates. The consumption of seafood, seaweed, rice and other food with high arsenic contents and the extent of cooking and arsenic-containing water used in food preparation may also interfere with the presentation of the urinary arsenic profile. Future studies are necessary to clarify the effects of the various arsenic metabolites including the trivalent methylated forms on the development of arsenic-induced human diseases with the consideration of the effects of confounding factors and the interactions with other effect modifiers.
Author Tseng, Chin-Hsiao
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IEDL.DBID AIKHN
ISSN 0041-008X
1096-0333
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IsPeerReviewed true
IsScholarly true
Issue 3
Keywords Environmental exposure
Human health
Toxicology
Arsenic metabolism
Water pollutants
Water
Human
Arsenic
Environmental factor
Exposure
Review
Metabolism
Carcinogen
Pollutant
Health and environment
Environment
Methylation
Bibliographic review
Public health
Language English
License https://www.elsevier.com/tdm/userlicense/1.0
CC BY 4.0
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content type line 23
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PMID 19168087
PQID 20406003
PQPubID 23462
PageCount 13
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proquest_miscellaneous_66981512
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pubmed_primary_19168087
pascalfrancis_primary_21234844
crossref_citationtrail_10_1016_j_taap_2008_12_016
crossref_primary_10_1016_j_taap_2008_12_016
elsevier_sciencedirect_doi_10_1016_j_taap_2008_12_016
ProviderPackageCode CITATION
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PublicationCentury 2000
PublicationDate 2009-03-15
PublicationDateYYYYMMDD 2009-03-15
PublicationDate_xml – month: 03
  year: 2009
  text: 2009-03-15
  day: 15
PublicationDecade 2000
PublicationPlace Amsterdam
PublicationPlace_xml – name: Amsterdam
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PublicationTitle Toxicology and applied pharmacology
PublicationTitleAlternate Toxicol Appl Pharmacol
PublicationYear 2009
Publisher Elsevier Inc
Elsevier
Publisher_xml – name: Elsevier Inc
– name: Elsevier
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Snippet Subjects exposed to arsenic show significant inter-individual variation in urinary patterns of arsenic metabolites but insignificant day-to-day...
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SubjectTerms 60 APPLIED LIFE SCIENCES
ALCOHOLS
ARSENIC
Arsenic - metabolism
Arsenic Poisoning - epidemiology
Arsenic Poisoning - etiology
Arsenic Poisoning - metabolism
Biological and medical sciences
Carcinogenesis, carcinogens and anticarcinogens
Chemical agents
Chemical and industrial products toxicology. Toxic occupational diseases
CHILDREN
Environment. Living conditions
ENVIRONMENTAL EXPOSURE
Environmental Exposure - adverse effects
Environmental Pollutants - adverse effects
Environmental Pollutants - metabolism
ESTROGENS
EXCRETION
Female
Human health
Humans
Male
Medical sciences
MEN
METABOLISM
METABOLITES
Metals and various inorganic compounds
METHYLATION
Oryza sativa
POLLUTANTS
PREGNANCY
PUBLIC HEALTH
Public health. Hygiene
Public health. Hygiene-occupational medicine
RICE
Risk Factors
SEAFOOD
SEAWEEDS
TOXICITY
Toxicology
Tumors
Water pollutants
Title A review on environmental factors regulating arsenic methylation in humans
URI https://dx.doi.org/10.1016/j.taap.2008.12.016
https://www.ncbi.nlm.nih.gov/pubmed/19168087
https://www.proquest.com/docview/20406003
https://www.proquest.com/docview/66981512
https://www.osti.gov/biblio/21182761
Volume 235
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