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A study of the potential for a herbicide formulation containing 2,4-d and picloram to cause male-mediated developmental toxicity in rats.

Authors :
Oakes DJ
Webster WS
Brown-Woodman PD
Ritchie HE
Source :
Toxicological sciences : an official journal of the Society of Toxicology [Toxicol Sci] 2002 Jul; Vol. 68 (1), pp. 200-6.
Publication Year :
2002

Abstract

Male Vietnam veterans have repeatedly expressed concern that exposure to herbicides in Vietnam may have caused birth defects in their offspring. The second most used herbicide was a mixture of 2,4-D and picloram called Agent White. This study is an investigation into the possible male-mediated reproductive toxicology of this herbicide. Male rats were gavaged for 5 days per week for 9 weeks with a mixture of 2,4-D and picloram called Tordon 75D(R) (the Australian derivative of Agent White). Three doses were tested; the high dose was considered the maximum tolerated dose. Each male was mated with two untreated females during weeks 2 and 3, 4 and 5, and 8 and 9 of treatment, and with four untreated females after an 11-week recovery period. Negative controls were males dosed with distilled water, and positive controls were males dosed with cyclophosphamide at 5.1 mg/kg/day. All mated females were killed on day 20 of gestation, and the fetuses were weighed and examined for either structural malformations or skeletal development. Litter size, fetal weight, and malformation rate were all unaffected by treatment. The cyclophosphamide positive controls showed the expected large increase in postimplantation loss. In general, within the limitations of the power of the study, the results did not show any evidence that exposure to a herbicide formulation containing 2,4-D and picloram is likely to cause male-mediated birth defects or other adverse reproductive outcomes.

Details

Language :
English
ISSN :
1096-6080
Volume :
68
Issue :
1
Database :
MEDLINE
Journal :
Toxicological sciences : an official journal of the Society of Toxicology
Publication Type :
Academic Journal
Accession number :
12075122
Full Text :
https://doi.org/10.1093/toxsci/68.1.200