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首页> 外文期刊>Regulatory Toxicology and Pharmacology: RTP >28-day repeated dose oral toxicity of recombinant human holo-lactoferrin in rats.
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28-day repeated dose oral toxicity of recombinant human holo-lactoferrin in rats.

机译:重组人全乳铁蛋白对大鼠的28天重复剂量口服毒性。

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摘要

Recombinant human holo-lactoferrin (holo-rhLF) was orally administered, via gavage, to Wistar rats at 1000, 500 and 100mg/kgbw/day for 28 days. The test article, holo-rhLF, was expressed in rice grain, extracted, purified and saturated with iron. During the 28-day period, animals were examined for evidence of toxicity. On day 29, the animals were exsanguinated, examined for gross pathology, and tissues preserved for histopathology. There were no deaths caused by holo-rhLF and in-life physical signs were generally normal. Although statistical differences were noted in some hematology, clinical chemistry and heart/body weight ratios, they were of questionable biological significance. A significantly greater total iron binding capacity (TIBC) was detected in the blood of male animals dosed with holo-rhLF. Serum was analyzed for the presence of IgG and IgE antibodies; demonstrating low levels of IgG antibodies to the human protein, but no increase in IgE antibodies. There was no increase in serum lactoferrin levels. The results of the 28-day oral administration demonstrate a lack of toxicity of holo-rhLF in rats. There were no treatment related, toxicologically relevant changes in clinical signs, growth, food consumption, hematology, clinical chemistry, organ weights or pathology. The no observed adverse effect level (NOAEL) is greater than 1000 mg/kg/day.
机译:通过强饲法向Wistar大鼠口服重组人全乳乳铁蛋白(holo-rhLF),剂量为1000、500和100mg / kgbw /天,持续28天。测试物品holo-rhLF在稻米中表达,提取,纯化并用铁饱和。在28天期间,检查了动物的毒性证据。在第29天,将动物放血,检查总体病理,并保存组织以进行病理学检查。没有由holo-rhLF引起的死亡,生命中的体征通常是正常的。尽管在某些血液学,临床化学和心脏/体重比中注意到统计学差异,但它们在生物学意义上存在可疑之处。在用holo-rhLF给药的雄性动物的血液中检测到明显更高的总铁结合能力(TIBC)。分析血清中IgG和IgE抗体的存在;证明针对人蛋白质的IgG抗体水平较低,但IgE抗体没有增加。血清乳铁蛋白水平没有增加。口服28天的结果表明,holo-rhLF在大鼠中没有毒性。在临床体征,生长,食物消耗,血液学,临床化学,器官重量或病理学方面,没有与治疗有关的,与毒理学相关的变化。未观察到不良反应水平(NOAEL)大于1000 mg / kg /天。

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