首页> 外文期刊>Journal of applied toxicology >Distribution of carbon-14 labeled C60 ((14C)C60) in the pregnant and in the lactating dam and the effect of C60 exposure on the biochemical profile of urine.
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Distribution of carbon-14 labeled C60 ((14C)C60) in the pregnant and in the lactating dam and the effect of C60 exposure on the biochemical profile of urine.

机译:碳14标记的C60((14C)C60)在孕妇和哺乳期大坝中的分布以及C60暴露对尿液生化特征的影响。

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This study was conducted to determine the distribution of [(14)C]C60 in the pregnant rat and fetuses, and in the lactating rat and offspring. Pregnant rats were dosed on gestation day (gd) 15 and lactating rats were dosed on postnatal day (pnd) 8 via tail vein injection with a suspension of approximately 0.3 mg [(14)C]C60 kg(-1) body weight prepared in polyvinylpyrrolidone (PVP), or with PVP alone. Tissues were collected at 24 and 48 h after dosing. The largest portion of the administered dose was detected in the liver (approximately 43%, pregnant dam; approximately 35%, lactating dam) and lung (approximately 25%, lactating dam). Radioactivity (approximately 6%) was distributed to the reproductive tract, placenta and fetuses of the pregnant dam. Lactating rats had radioactivity distributed to the milk (3140 dpm g(-1) tissue, 24 h; 1620 dpm g(-1) tissue, 48 h), and to the pups' GI tract (2.8%, 24 h; 4.4% 48 h) and liver (<1%). Blood radioactivity was significant at 24 h (14-19%) and at 48 h (7%) after dosing; largely accounted for in the plasma fraction. Less that 4% of the dose was recovered in the maternal spleen, heart, brain, urine or feces. Metabolomics analysis of urine indicated that dams exposed to [(14)C]C60 had decreased metabolites derived from the Krebs cycle and increased metabolites derived from the urea cycle or glycolysis, as well as alterations in the levels of some sulfur-containing amino acids and purine/pyrimidine metabolites. This study demonstrated that [(14)C]C60 crosses the placenta and is transmitted to offspring via the dam's milk and subsequently systemically absorbed.
机译:进行这项研究,以确定[(14)C] C60在怀孕的大鼠和胎儿,以及在哺乳的大鼠和后代中的分布。妊娠大鼠在妊娠第15天给药,哺乳期大鼠在出生后第8天给药,通过尾静脉注射约0.3 mg [(14)C] C60 kg(-1)体重的混悬液制备。聚乙烯吡咯烷酮(PVP),或单独使用PVP。给药后24和48小时收集组织。在肝脏(大约43%,妊娠大坝;大约35%,泌乳大坝)和肺部(大约25%,泌乳大坝)中检测到最大剂量的给药。放射性(约6%)被分配到怀孕大坝的生殖道,胎盘和胎儿。哺乳期大鼠的放射性分布于牛奶(3140 dpm g(-1)组织,24 h; 1620 dpm g(-1)组织,48 h)和幼仔的胃肠道(2.8%,24 h; 4.4%) 48小时)和肝脏(<1%)。给药后24 h(14-19%)和48 h(7%)的血液放射性显着;在血浆中占很大比例。在孕妇的脾脏,心脏,大脑,尿液或粪便中回收的剂量不足4%。尿液的代谢组学分析表明,暴露于[(14)C] C60的水坝,其克雷布斯循环产生的代谢物减少,尿素循环或糖酵解产生的代谢物增加,并且某些含硫氨基酸和嘌呤/嘧啶代谢产物。这项研究表明,[(14)C] C60穿过胎盘,并通过大坝的牛奶传播给后代,随后被全身吸收。

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