赭曲霉毒素A在大鼠胎盘及哺乳期的转移。

I P Hallén, A Breitholtz-Emanuelsson, K Hult, M Olsen, A Oskarsson
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引用次数: 32

摘要

在大鼠的交叉培养研究中,研究了赭曲霉毒素A (OA)在胎盘和哺乳期的转移。在交配前2周、妊娠期间和哺乳期每周7天,通过胃插管给药50 mg OA(-1) kg体重,每周5次。从oa处理坝的新生儿在出生时交叉培养,以控制仅用载体处理的坝。同样,对照坝的幼崽也被交叉培养到经oa处理的坝中。在出生后的前21天,OA治疗对幼崽的出生体重或生长发育没有任何影响。以乳脂、蛋白质或乳糖浓度衡量的牛奶质量没有受到影响,以乳腺RNA和DNA含量评估的产奶量也没有受到影响。平均乳血比约为0.6。14日龄幼犬从乳汁中摄取的OA剂量可计算为约50 μ g kg(-1)体重(-1)天,这与给坝的剂量相似。仅通过乳汁接触OA的幼崽血液和肾脏中的OA水平约为其母鼠的3倍,这表明幼崽对OA的吸收率高,排泄量低。在14日龄时,通过胎盘和乳汁暴露的后代血液和肾脏中OA水平最高,其中乳汁的贡献最大。与仅通过胎盘接触的后代相比,仅通过牛奶接触的后代血液和肾脏中的OA水平高出4-5倍。由于牛奶可能是新生儿接触OA的一个重要来源,因此在OA风险评估中应研究和评估产后接触OA对健康造成的不利影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Placental and lactational transfer of ochratoxin A in rats.

The placental and lactational transfer of ochratoxin A (OA) was investigated in a cross-fostering study in rats. Dams were given 50 microg OA(-1) kg body weight by gastric intubations 5 times a week for 2 weeks before mating, during gestation and then 7 days a week during lactation. Neonates from OA-treated dams were cross-fostered at birth to control dams treated with only vehicle. In the same way, neonates from control dams were cross-fostered to OA-treated dams. Treatment with OA did not result in any effects on birth weight or growth development of the pups during the first 21 days of life. There were no effects on milk quality as measured by milk lipids, protein or lactose concentrations, or on milk production, assessed by the mammary gland content of RNA and DNA. A mean milk:blood ratio of approximately 0.6 was found. The dose of OA from milk to the suckling pup at 14 days of age can be calculated to about 50 microg kg(-1) body weight(-1) day, which is similar to the dose given to the dams. Pups exposed to OA only via milk had blood and kidney levels of OA approximately 3 times higher than their dams, indicating a high absorption and/or a low excretion of OA in the sucklings. At 14 days of age the highest blood and kidney levels of OA were found in offspring exposed both via placenta and milk, with the highest contribution from milk. Offspring exposed only via milk had about 4-5 times higher levels of OA in blood and kidney compared to offspring exposed only via placenta. As milk could be a significant source of OA exposure in newborns, adverse health effects resulting from postnatal exposure should be studied and evaluated in the risk assessment of OA.

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