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Long-lasting developmental effects in rat offspring after maternal exposure to acetamiprid in the drinking water during gestation

后代 妊娠期 发育毒性 怀孕 胎儿 畸形学 生理学 毒性 肛门生殖距离 生殖毒性 毒理 未观察到不良反应水平 生物 医学 内科学 子宫内 遗传学
作者
Victoria Longoni,Paula C. Kandel Gambarte,L. Baila Rueda,J. Fuchs,María Gabriela Rovedatti,Marcelo Javier Wolansky
出处
期刊:Toxicological Sciences [Oxford University Press]
标识
DOI:10.1093/toxsci/kfad122
摘要

Neonicotinoids (NNTs) are a class of insecticides proposed to be safe for pest control in urban, suburban and agricultural applications. However, little is known about their developmental effects after repeated low-dose exposures during gestation. Here, we tested a dose considered subthreshold for maternal toxicity in rats (6 mg/kg/day) by assessing several morphological, biochemical and neurobehavioral features in pre-term fetuses and developing pups after maternal administration of the NTT acetamiprid (ACP) dissolved in the drinking water during gestational days (GD) 2-19. The exploratory evaluation included monitoring maternal body weight gain, fetal viability, body weight and sex ratio, cephalic length, neonatal body weight and sex ratio, metabolic enzymes in the placenta, maternal blood, and fetal liver, anogenital distance and surface righting response during infancy. We also used the Circling Training Test to study the integrity of the associative-spatial-motor response in adolescence. Results showed no consistent findings indicating maternal, reproductive or developmental toxicity. However, we found ACP effects on maternal body weight gain, placental butyrylcholinesterase activity and neurobehavioral responses, suggestive of a mild toxic action. Thus, our study showed a trend for developmental susceptibility at a dose so far considered subtoxic. Although the ACP concentration in environmental samples of surface water and groundwater has been mostly reported to be much lower than that used in our study, our results suggest that the ACP point of departure used in current guidelines aimed to prevent developmental effects may need to be verified by complementary sensitive multiple-endpoint testing in the offspring.

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