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首页> 外文期刊>Drug and Chemical Toxicology >Developmental toxicity of steviol, a metabolite of stevioside, in the hamster.
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Developmental toxicity of steviol, a metabolite of stevioside, in the hamster.

机译:甜菊糖,一种甜菊糖的代谢产物,对仓鼠的发育毒性。

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摘要

The developmental toxicity of steviol, a metabolite of stevioside, was studied in hamsters. Pregnant hamsters were intubated with steviol at dose levels of 0, 0.25, 0.5, 0.75 and 1.0 g/kg BW/day on days 6-10 of gestation. Steviol at doses of 0.75 and 1.0 g/kg BW/day were highly toxic to both dams and fetuses. Significant decrease of maternal body-weight gain during the experimental period (days 6-14) and high percentage of maternal mortality indicated the general toxicity of these two high doses. The number of live fetuses per litter and mean fetal weight also significantly decreased in the steviol-treated animals at doses of 0.75 and 1.0 g/kg BW day. The animals treated with an intermediate dose (0.50 g/kg BW/day) exhibited less signs of maternal and developmental toxicity than the two high doses (0.75 and 1.0 g/kg BW/day). One craniomeningocele was found in a fetus under the maternal toxic condition in steviol-treated at a dose of 0.75 g/kg BW/day. Neither the skeleton nor visceral development of the offspring was affected by steviol treatment except delayed ossification of the xiphoid (bifid) and long bones of the limbs and supernumerary thoracic ribs (14th ribs) tended to be increased at doses of 0.5 to 1.0 g/kg BW/day steviol. No dose-related teratogenesis was detected. From the result of the present study concerning maternal toxic condition and embryotoxicity, an oral dose of 0.25 g steviol/kg BW/day is regarded as having no observable effect. This steviol-treated dose is derived from stevioside 625 mg/kg BW/day which is approximately 80 times higher than the suggested acceptable daily intake of stevioside for humans (7.938 mg/kg BW/day).
机译:在仓鼠中研究了甜菊醇(一种甜菊糖的代谢产物)的发育毒性。在妊娠的第6-10天,以0、0.25、0.5、0.75和1.0 g / kg BW /天的剂量水平向甜味仓鼠插入妊娠仓鼠。 0.75和1.0 g / kg BW /天的甜菊醇对大坝和胎儿均具有高毒性。在实验期间(第6至14天)孕妇体重增加显着下降,且孕妇死亡率高表明这两种高剂量的一般毒性。在每天接受0.75和1.0 g / kg BW剂量的甜菊醇处理的动物中,每窝活胎儿的数量和平均胎儿体重也明显减少。与两次高剂量(0.75和1.0 g / kg BW /天)相比,以中等剂量(0.50 g / kg BW /天)治疗的动物表现出更少的母体和发育毒性迹象。在母体毒性条件下,以0.75 g / kg BW /天的剂量进行了甜菊醇处理的胎儿中发现了一个颅骨膨大。甜菊醇处理对子代的骨骼和内脏发育均没有影响,除了剑突(双歧)的骨化延迟和四肢的长骨和多余的胸肋骨(第14肋骨)的剂量在0.5至1.0 g / kg时倾向于增加体重/天甜菊醇。未检测到剂量相关的致畸作用。从有关母体毒性状况和胚胎毒性的本研究结果来看,口服剂量0.25 g甜菊醇/ kg BW /天被认为没有明显效果。甜菊糖治疗的剂量源自甜菊糖625 mg / kg体重/天,这比建议的人类每日可接受的甜菊糖的可接受每日摄入量(7.938 mg / kg体重/天)高约80倍。

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