A review on environmental factors regulating arsenic methylation in humans
Creators
- 1. Division of Environmental Health and Occupational Medicine of the National Health Research Institutes, Taipei, Taiwan (China)
- 2. School of Public Health, Taipei Medical University, Taipei, Taiwan (China)
- 3. Department of Medical Research and Development, National Taiwan University Hospital Yun-Lin Branch, Yun-Lin, Taiwan (China)
- 4. Division of Endocrinology and Metabolism, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan (China)
- 5. National Taiwan University College of Medicine, Taipei, Taiwan (China)
Description
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
Availability note (English)
Available from http://dx.doi.org/10.1016/j.taap.2008.12.016Additional details
Identifiers
- DOI
- 10.1016/j.taap.2008.12.016;
- PII
- S0041-008X(08)00529-2;
Publishing Information
- Journal Title
- Toxicology and Applied Pharmacology
- Journal Volume
- 235
- Journal Issue
- 3
- Journal Page Range
- p. 338-350
- ISSN
- 0041-008X
- CODEN
- TXAPA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 40057010
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ALCOHOLS; ARSENIC; CHILDREN; ENVIRONMENTAL EXPOSURE; ESTROGENS; EXCRETION; MEN; METABOLISM; METABOLITES; METHYLATION; POLLUTANTS; PREGNANCY; PUBLIC HEALTH; RICE; SEAFOOD; SEAWEEDS; TOXICITY
- Descriptors DEC
- AGE GROUPS; ANIMALS; AQUATIC ORGANISMS; CEREALS; CHEMICAL REACTIONS; CLEARANCE; ELEMENTS; FISH PRODUCTS; FOOD; GRAMINEAE; HORMONES; HYDROXY COMPOUNDS; LILIOPSIDA; MAGNOLIOPHYTA; MALES; MAMMALS; MAN; ORGANIC COMPOUNDS; PLANTS; PRIMATES; SEMIMETALS; STEROID HORMONES; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2009 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.