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山梨酸给药对低剂量苯暴露大鼠尿中反式、反式粘康酸排泄的影响。

Effect of sorbic acid administration on urinary trans,trans-muconic acid excretion in rats exposed to low levels of benzene.

作者信息

Marrubini G, Coccini T, Maestri L, Manzo L

机构信息

Laboratory for Pharmacokinetics and Analytical Toxicology, Clinical Toxicology Division, Department of Internal Medicine, University of Pavia, Via Brodolini 7, 27028 San Martino Siccomario, Italy.

出版信息

Food Chem Toxicol. 2002 Dec;40(12):1799-806. doi: 10.1016/s0278-6915(02)00185-0.

Abstract

Trans,trans-muconic acid (t,t-MA) is a biomarker of benzene exposure reflecting metabolic activation to trans,trans-muconaldehyde. t,t-MA background urinary levels are highly variable, thus limiting its use to exposure monitoring of levels over 1 ppm of benzene. Actually, sorbic acid (SA) is known to influence background excretion of t,t-MA in man, but only a few examples suggest that SA ingestion can enhance t,t-MA levels occurring together with benzene exposure. In this study, the effect of SA was investigated in benzene-exposed male Sprague-Dawley rats exposed to 1 ppm benzene for 6 h. Exposed animals had a 24-h urinary t,t-MA excretion higher than that observed in non-exposed animals (87+/-13 microg/kg vs 19+/-3 microg/kg body weight). The oral dose of 8 mg/kg body weight SA had no effect on urinary t,t-MA both in control and in benzene-exposed rats. Increases of t,t-MA levels in urine occurred at SA doses of 50-200 mg/kg body weight, and co-exposure to benzene and SA (50 and 100 mg/kg body weight) produced additive enhancement of t,t-MA excretion. These data demonstrate the dose-response relationship between SA administration and t,t-MA excretion. Our study showed that SA ingestion at doses equal to or greater than 50 mg/kg body weight significantly affects the t,t-MA urinary levels in rats exposed to 1 ppm of benzene for 6 h. These data support the conclusion that in man t,t-MA is not suitable for biomonitoring of low levels of benzene exposure.

摘要

反式,反式-粘康酸(t,t-MA)是苯暴露的生物标志物,反映了向反式,反式-粘康醛的代谢活化。t,t-MA的背景尿水平变化很大,因此限制了其在监测苯暴露水平超过1 ppm时的应用。实际上,已知山梨酸(SA)会影响人体中t,t-MA的背景排泄,但只有少数例子表明摄入SA可提高与苯暴露同时出现的t,t-MA水平。在本研究中,研究了SA对暴露于1 ppm苯6小时的雄性Sprague-Dawley大鼠的影响。暴露动物的24小时尿t,t-MA排泄量高于未暴露动物(87±13微克/千克体重vs 19±3微克/千克体重)。口服8毫克/千克体重的SA对对照组和苯暴露大鼠的尿t,t-MA均无影响。当SA剂量为50-200毫克/千克体重时,尿中t,t-MA水平升高,同时暴露于苯和SA(50和100毫克/千克体重)会使t,t-MA排泄量产生相加性增加。这些数据证明了SA给药与t,t-MA排泄之间的剂量反应关系。我们的研究表明,摄入剂量等于或大于50毫克/千克体重的SA会显著影响暴露于1 ppm苯6小时的大鼠的尿t,t-MA水平。这些数据支持了t,t-MA不适用于人体低水平苯暴露生物监测的结论。

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