Developmental toxicity studies in rats and rabbits on 2,4-dichlorophenoxyacetic acid and its forms

Citation
Jm. Charles et al., Developmental toxicity studies in rats and rabbits on 2,4-dichlorophenoxyacetic acid and its forms, TOXICOL SCI, 60(1), 2001, pp. 121-131
Citations number
52
Categorie Soggetti
Pharmacology & Toxicology
Journal title
TOXICOLOGICAL SCIENCES
ISSN journal
10966080 → ACNP
Volume
60
Issue
1
Year of publication
2001
Pages
121 - 131
Database
ISI
SICI code
1096-6080(200103)60:1<121:DTSIRA>2.0.ZU;2-B
Abstract
The potential for 2,4-D and its salts and esters to induce developmental to xicity was investigated in rats (8 studies) and rabbits (7 studies). Matern al toxicity associated with exposure was dependent on the dose level expres sed as 2,4-D acid equivalents. The severity of the maternal effect was corr elated to the 2,4-D acid-equivalent dose, with increasing dose levels that exceeded renal clearance causing increasingly more severe maternal effects. In both species, maternal body weight effects began to be manifested at do se levels of 30 mg 2,4-D acid equivalent/kg/day. At higher dose levels (50- 75 mg/kg/day in rats and 75-90 mg/kg/day in rabbits), body weights and feed consumption were more severely affected. At dose levels greater than or eq ual to 90 mg/kg/day in rats, clinical signs of toxicity (ataxia, muscular s tiffness, and decreased motor activity) and mortality were noted. The no-ob served-adverse-effect level (NOAEL) for maternal toxicity in both species a cross the family of 2,4-D salts and esters was approximately 10 mg/kg/day. Significantly decreased fetal body weights and increased fetal variations w ere seen in rats only at maternally toxic dose levels in excess of 90 mg/kg /day acid equivalent. At maternally toxic doses in rabbits, embryonal and f etal development were essentially unaffected. There were no effect on mater nal reproductive measures such as litter size, resorption rates, or fetal b ody weights, and there was no evidence of teratogenic activity. In summary, equivalent toxicity of the salts and esters is consistent with rapid and c omplete metabolic conversion to 2,4-D acid. No adverse fetal effects were n oted at dose levels that did not also produce evidence of maternal toxicity or exceed renal clearance of 2,4-D indicating that the developing rat and rabbit fetus were not uniquely sensitive to 2,4-D and its forms.