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首页> 外文期刊>The Journal of toxicological sciences >Lack of micronucleus induction activity of ethyl tertiary-butyl ether in the bone marrow of F344 rats by sub-chronic drinking-water treatment, inhalation exposure, or acute intraperitoneal injection
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Lack of micronucleus induction activity of ethyl tertiary-butyl ether in the bone marrow of F344 rats by sub-chronic drinking-water treatment, inhalation exposure, or acute intraperitoneal injection

机译:亚慢性饮用水处理,吸入暴露或急性腹膜内注射对F344大鼠骨髓中乙基叔丁基醚的微核诱导活性缺乏

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摘要

Ethyl tertiary-butyl ether (ETBE) is an oxygenated gasoline additive synthesized from ethanol and isobutene that is used to reduce CO2 emissions. To support the Kyoto Protocol, the production of ETBE has undergone a marked increase. Previous reports have indicated that exposure to ETBE or methyl tertiary-butyl ether resulted in liver and kidney tumors in rats and/or mice. These reports raise concern about the effects of human exposure being brought about by the increased use of ETBE. The present study was conducted to evaluate the genotoxicity of ETBE using micronucleus induction of polychromatic erythrocytes in the bone marrow of male and female rats treated with ETBE in the drinking-water at concentrations of 0, 1,600, 4,000 or 10,000 ppm or exposed to ETBE vapor at 0, 500, 1,500 or 5,000 ppm for 13 weeks. There were no significant increases in micronucleus induction in either the drinking water-administered or inhalation-administered groups at any concentration of ETBE; although, in both groups red blood cells and hemoglobin concentration were slightly reduced in the peripheral blood in rats administered the highest concentration of ETBE. In addition, two consecutive daily intraperitoneal injections of ETBE at doses of 0, 250, 500 or 1,000 mg/kg did not increase the frequency of micronucleated bone marrow cells in either sex; all rats receiving intraperitoneal injections of ETBE at a dose of 2,000 mg/kg died after treatment day 1. These data suggest that ETBE is not genotoxic in vivo.
机译:乙基叔丁基醚(ETBE)是一种由乙醇和异丁烯合成的含氧汽油添加剂,用于减少CO2排放。为了支持《京都议定书》,ETBE的产量有了明显增长。先前的报道表明,暴露于ETBE或甲基叔丁基醚会导致大鼠和/或小鼠的肝肾肿瘤。这些报告引起了人们的关注,即日益增加的ETBE使用量对人体暴露的影响。本研究旨在通过在饮用水中浓度为0、1,600、4,000或10,000 ppm或暴露于ETBE蒸气中的ETBE处理的雄性和雌性大鼠的骨髓中多色红细胞的微核诱导来评估ETBE的遗传毒性在0、500、1,500或5,000 ppm的情况下保持13周。在任何浓度的ETBE中,饮水组或吸入组的微核诱导均无明显增加。尽管在两组中,给予最高浓度ETBE的大鼠外周血中的红细胞和血红蛋白浓度均略有降低。此外,连续两次每天两次以0、250、500或1,000 mg / kg的剂量腹腔注射ETBE不会增加男女中微核骨髓细胞的频率。在治疗第1天后,所有接受2,000 mg / kg剂量的ETBE腹腔注射的大鼠均死亡。这些数据表明ETBE在体内没有遗传毒性。

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