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大鼠嗅黏膜在代谢甲基叔丁基醚和其他汽油醚方面表现出高活性。

Rat olfactory mucosa displays a high activity in metabolizing methyl tert-butyl ether and other gasoline ethers.

作者信息

Hong J Y, Wang Y Y, Bondoc F Y, Yang C S, Lee M, Huang W Q

机构信息

Department of Chemical Biology, College of Pharmacy, Rutgers University, Piscataway, New Jersey 08854, USA.

出版信息

Fundam Appl Toxicol. 1997 Dec;40(2):205-10. doi: 10.1006/faat.1997.2383.

Abstract

Methyl tert-butyl ether (MTBE) is a widely used gasoline oxygenate. Two other ethers, ethyl tert-butyl ether (ETBE) and tert-amyl methyl ether (TAME), are also used in reformulated gasoline. Inhalation is a major route for human exposure to MTBE and other gasoline ethers. The possible adverse effects of MTBE in humans are a public concern and some of the reported symptoms attributed to MTBE exposure appear to be related to olfactory sensation. In the present study, we have demonstrated that the olfactory mucosa of the male Sprague-Dawley rat possesses the highest microsomal activities, among the tissues examined, in metabolizing MTBE, ETBE, and TAME. The metabolic activity of the olfactory mucosa was 46-fold higher than that of the liver in metabolizing MTBE, and 37- and 25-fold higher, respectively, in metabolizing ETBE and TAME. No detectable activities were found in the microsomes prepared from the lungs, kidneys, and olfactory bulbs of the brain. The observations that the metabolic activity was localized exclusively in the microsomal fraction, depended on the presence of NADPH, and was inhibitable by carbon monoxide are consistent with our recent report on MTBE metabolism in human and mouse livers (Hong et al., 1997) and further confirm that cytochrome P450 enzymes play a critical role in the metabolism of MTBE, ETBE, and TAME. The apparent K(m) and Vmax values for the metabolism of MTBE, ETBE, and TAME in rat olfactory microsomes were very similar, ranging from 87 to 125 microM and 9.8 to 11.7 nmol/min/mg protein, respectively. Addition of TAME (0.1 to 0.5 mM) into the incubation mixture caused a concentration-dependent inhibition of the metabolism of MTBE and ETBE. Coumarin (50 microM) inhibited the metabolism of these ethers by approximately 87%. Further comparative studies with human nasal tissues on the metabolism of these ethers are needed in order to assess the human relevance of our present findings.

摘要

甲基叔丁基醚(MTBE)是一种广泛使用的汽油含氧化合物。另外两种醚类,即乙基叔丁基醚(ETBE)和叔戊基甲基醚(TAME),也用于新配方汽油中。吸入是人类接触MTBE和其他汽油醚的主要途径。MTBE对人类可能产生的不良影响是公众关注的问题,一些报告称归因于MTBE暴露的症状似乎与嗅觉有关。在本研究中,我们已经证明,在检测的组织中,雄性斯普拉格-道利大鼠的嗅觉黏膜在代谢MTBE、ETBE和TAME方面具有最高的微粒体活性。嗅觉黏膜在代谢MTBE时的代谢活性比肝脏高46倍,在代谢ETBE和TAME时分别高37倍和25倍。在从肺、肾和脑的嗅球制备的微粒体中未发现可检测到的活性。代谢活性仅局限于微粒体部分、依赖于NADPH的存在且可被一氧化碳抑制的观察结果与我们最近关于人和小鼠肝脏中MTBE代谢的报告(Hong等人,1997年)一致,并进一步证实细胞色素P450酶在MTBE、ETBE和TAME的代谢中起关键作用。大鼠嗅觉微粒体中MTBE、ETBE和TAME代谢的表观K(m)和Vmax值非常相似,分别为87至125 microM和9.8至11.7 nmol/min/mg蛋白质。向孵育混合物中添加TAME(0.1至0.5 mM)会导致MTBE和ETBE代谢的浓度依赖性抑制。香豆素(50 microM)使这些醚类的代谢受到约87%的抑制。为了评估我们目前研究结果与人类的相关性,需要对人类鼻组织进行关于这些醚类代谢的进一步比较研究。

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