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首页> 外文期刊>Archives of Toxicology >Comparative toxicokinetic/toxicodynamic study of rubber antioxidants, 2-mercaptobenzimidazole and its methyl substituted derivatives, by repeated oral administration in rats.
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Comparative toxicokinetic/toxicodynamic study of rubber antioxidants, 2-mercaptobenzimidazole and its methyl substituted derivatives, by repeated oral administration in rats.

机译:通过在大鼠中反复口服给药,对橡胶抗氧化剂,2-巯基苯并咪唑及其甲基取代的衍生物进行了比较的毒代动力学/毒理动力学研究。

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2-Mercaptobenzimidazole (MBI), a rubber antioxidant, is known to exhibit potent thyroid toxicity in rats, whereas its methylated derivatives are much less toxic. To characterize this methyl-substituent effect on the thyroid toxicity of MBI, comparative toxicokinetic analyses have been conducted in the present study. MBI and the MMBIs [4-methylated MBI (4-MMBI) and 5-methylated MBI (5-MMBI), and a 1:1 mixture of these 4- and 5-methylated isomers (MMBI mix)] suspended in corn oil were repeatedly administered (at 0.3-0.6 mmol/kg) to male Wistar rats by gavage once daily for 2 weeks. After the first and last administrations, blood and urine samples were collected, and the levels of unchanged compounds and their desulfurated metabolites were determined by high performance liquid chromatography. After repeated oral administration (roa), the C(max) and area under concentration-time curve (AUC) of MBI were markedly increased, while the MMBIs essentially were cleared from the blood within 10 h. After roa, the C(max) and AUC of 4-MMBI decreased markedly, suggesting metabolic enzyme induction. However, the toxicokinetic parameters of 5-MMBI were not markedly altered by roa. The inhibitory potencies (IC(50)) against lactoperoxidase of MBI, 4-MMBI, and 5-MMBI were 20.6 micro M, 45.6 micro M and 31.6 micro M, respectively. Thus, we suggest that the marked decrease of thyroid toxicity by methyl substitution of MBI is caused mainly by a decrease in systemic exposure to the compounds and partly by a decrease in inhibition of thyroid hormone synthesis.
机译:众所周知,橡胶抗氧化剂2-巯基苯并咪唑(MBI)在大鼠中表现出强大的甲状腺毒性,而其甲基化衍生物的毒性则小得多。为了表征这种甲基取代基对MBI甲状腺毒性的作用,在本研究中进行了比较毒代动力学分析。悬浮在玉米油中的MBI和MMBIs [4-甲基化MBI(4-MMBI)和5-甲基化MBI(5-MMBI),以及这些4-和5-甲基化异构体的1:1混合物(MMBI混合物)]每天一次通过管饲法对雄性Wistar大鼠重复给药(0.3-0.6 mmol / kg),持续2周。第一次和最后一次给药后,收集血液和尿液样本,并通过高效液相色谱法测定未改变的化合物及其脱硫代谢产物的水平。反复口服(roa)后,MBI的C(max)和浓度-时间曲线下面积(AUC)显着增加,而MMBIs在10小时内从血液中清除。罗阿后,4-MMBI的C(max)和AUC明显下降,表明代谢酶诱导。但是,ROA并没有明显改变5-MMBI的毒代动力学参数。对MBI,4-MMBI和5-MMBI的乳过氧化物酶的抑制能力(IC(50))分别为20.6 micro M,45.6 micro M和31.6 microM。因此,我们认为通过MBI的甲基取代引起的甲状腺毒性的显着降低主要是由于与这些化合物的全身接触降低,部分是由于抑制了甲状腺激素合成所致。

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