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
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.