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Limited lactational transfer of acrylamide to rat offspring on maternal oral administration during the gestation and lactation periods.

机译:在妊娠期和哺乳期口服母体时,丙烯酰胺向大鼠后代的哺乳期转移有限。

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摘要

To evaluate the developmental exposure effects of acrylamide (ACR) on the nervous and male reproductive systems, pregnant Sprague-Dawley rats were given ACR at 0, 25, 50 or 100 ppm in the drinking water from gestational day 6 to postnatal day (PND) 21 and histopathological assessment was performed at PND 21. Exposure levels in offspring were examined by measurement of free ACR and hemoglobin (Hb)-ACR adducts on PND 14, and compared with maternal levels on PND 21. Additionally, a group of offspring that received ACR at 50 mg/kg by intraperitoneal injections directly three times a week from PND 2 to 21 was subjected to analysis for comparison with maternal exposure groups. Although maternal neurotoxicity was evident at 100 ppm, no changes suggestive of neurotoxicity or testicular toxicity were observed in their offspring except for growth retardation evident as lowered body weights. In contrast, offspring given ACR intraperitoneally exhibited obvious neurotoxicity, but not testicular damage. Free ACR in serum and milk was detected in neither dams nor their offspring. The level of ACR-Hb adducts in offspring was one tenth or less than that in dams. In summary, although preweaning rats have susceptibility to ACR-induced neurotoxicity, the internal level of ACR in offspring exposed through maternal oral administration is insufficient to induce neurotoxicity and testicular toxicity due to limited lactational transfer.
机译:为了评估丙烯酰胺(ACR)对神经和雄性生殖系统的发育暴露影响,从妊娠第6天到出生后(PND)的怀孕Sprague-Dawley大鼠在饮用水中分别以0、25、50或100 ppm给予ACR。 21,在PND 21进行组织病理学评估。通过测量PND 14上的游离ACR和血红蛋白(Hb)-ACR加合物,检查后代的暴露水平,并将其与PND 21上的母体水平进行比较。每周3次从PND 2至21直接腹膜内注射50 mg / kg的ACR进行分析,以与母体暴露组进行比较。尽管母体的神经毒性在100 ppm时很明显,但其后代没有观察到提示神经毒性或睾丸毒性的变化,除了体重减轻引起的生长迟缓以外。相反,腹膜内给予ACR的后代表现出明显的神经毒性,但没有睾丸损伤。大坝及其后代均未检测到血清和牛奶中的游离ACR。后代中ACR-Hb加合物的水平是水坝中十分之一或更少。总之,尽管断奶前的老鼠对ACR引起的神经毒性很敏感,但是由于母乳口服限制,母体口服给药后代暴露的ACR内部水平不足以诱发神经毒性和睾丸毒性。

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