Literature DB >> 10861633

Appropriate use of animal models in the assessment of risk during prenatal development: an illustration using inorganic arsenic.

J F Holson1, J M Desesso, C F Jacobson, C H Farr.   

Abstract

BACKGROUND: Assessing risks to human development from chemical exposure typically requires integrating findings from laboratory animal and human studies.
METHODS: Using a case study approach, we present a program designed to assess the risk of the occurrence of malformations from inorganic arsenic exposure. We discuss how epidemiological data should be evaluated for quality and criteria for determining whether an association is causal. In this case study, adequate epidemiological data were not available for evaluating the potential effect of arsenic on development. Consequently, results from appropriately designed, conducted, and interpreted developmental toxicity studies, which have been shown to be predictive of human risk under numerous scenarios, were used. In our case study, the existing animal data were not designed appropriately to assess risk from environmental exposures, although such studies may be useful for hazard identification. Because the human and animal databases were deficient, a research program comprising modern guideline toxicological studies was designed and conducted.
RESULTS: The results of those studies in rats, mice, and rabbits indicate that oral and inhalational exposures to inorganic arsenic do not cause structural malformations, and inhalational exposures produced no developmental effects at all. The new study results are discussed in conjunction with considerations of metabolism, toxicokinetics, and maternal toxicity.
CONCLUSIONS: Based on the available experimental data, and absent contrary findings from adequately conducted epidemiological studies, we conclude that exposure to inorganic arsenic by environmentally relevant routes poses no risk of the occurrence of malformations and little risk of other prenatal developmental toxicity in developing humans without concomitant and near-lethal toxicological effects in mothers. Copyright 2000 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10861633     DOI: 10.1002/1096-9926(200007)62:1<51::AID-TERA10>3.0.CO;2-T

Source DB:  PubMed          Journal:  Teratology        ISSN: 0040-3709


  10 in total

1.  Arsenicals in maternal and fetal mouse tissues after gestational exposure to arsenite.

Authors:  Vicenta Devesa; Blakely M Adair; Jie Liu; Michael P Waalkes; Bhalchandra A Diwan; Miroslav Styblo; David J Thomas
Journal:  Toxicology       Date:  2006-05-03       Impact factor: 4.221

2.  Embryonic toxicokinetic and dynamic differences underlying strain sensitivity to cadmium during neurulation.

Authors:  Joshua F Robinson; Xiaozhong Yu; Sungwoo Hong; Chunyan Zhou; Nayeon Kim; Davide DeMasi; Elaine M Faustman
Journal:  Reprod Toxicol       Date:  2009-12-16       Impact factor: 3.143

Review 3.  Bridging epidemiology and model organisms to increase understanding of endocrine disrupting chemicals and human health effects.

Authors:  Tracey J Woodruff
Journal:  J Steroid Biochem Mol Biol       Date:  2010-11-26       Impact factor: 4.292

4.  Developmental consequences of in utero sodium arsenate exposure in mice with folate transport deficiencies.

Authors:  Ofer Spiegelstein; Amy Gould; Bogdan Wlodarczyk; Marlene Tsie; Xiufen Lu; Chris Le; Aron Troen; Jacob Selhub; Jorge A Piedrahita; J Michael Salbaum; Claudia Kappen; Stepan Melnyk; Jill James; Richard H Finnell
Journal:  Toxicol Appl Pharmacol       Date:  2005-02-15       Impact factor: 4.219

5.  Learning deficits in C57BL/6J mice following perinatal arsenic exposure: consequence of lower corticosterone receptor levels?

Authors:  Ebany J Martinez-Finley; Abdul-Mehdi S Ali; Andrea M Allan
Journal:  Pharmacol Biochem Behav       Date:  2009-09-13       Impact factor: 3.533

6.  Systems biology and birth defects prevention: blockade of the glucocorticoid receptor prevents arsenic-induced birth defects.

Authors:  Bhavesh K Ahir; Alison P Sanders; Julia E Rager; Rebecca C Fry
Journal:  Environ Health Perspect       Date:  2013-01-03       Impact factor: 9.031

Review 7.  Hazard identification and predictability of children's health risk from animal data.

Authors:  LaRonda L Morford; Judith W Henck; William J Breslin; John M DeSesso
Journal:  Environ Health Perspect       Date:  2004-02       Impact factor: 9.031

8.  Association between arsenic, cadmium, manganese, and lead levels in private wells and birth defects prevalence in North Carolina: a semi-ecologic study.

Authors:  Alison P Sanders; Tania A Desrosiers; Joshua L Warren; Amy H Herring; Dianne Enright; Andrew F Olshan; Robert E Meyer; Rebecca C Fry
Journal:  BMC Public Health       Date:  2014-09-15       Impact factor: 3.295

9.  Arsenic Toxicity in Male Reproduction and Development.

Authors:  Yoon-Jae Kim; Jong-Min Kim
Journal:  Dev Reprod       Date:  2015-12

Review 10.  Gene Environment Interactions in the Etiology of Neural Tube Defects.

Authors:  Richard H Finnell; Carlo Donato Caiaffa; Sung-Eun Kim; Yunping Lei; John Steele; Xuanye Cao; Gabriel Tukeman; Ying Linda Lin; Robert M Cabrera; Bogdan J Wlodarczyk
Journal:  Front Genet       Date:  2021-05-10       Impact factor: 4.599

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.