Thier R, Wiebel F A, Hinkel A, Burger A, Brüning T, Morgenroth K, Senge T, Wilhelm M, Schulz T G
Institut für Arbeitsphysiologie an der Universität Dortmund, Germany.
Arch Toxicol. 1998 Oct;72(10):622-9. doi: 10.1007/s002040050552.
Glutathione transferase (GST) GSTT1-1 is involved in the biotransformation of several chemicals widely used in industry, such as butadiene and dichloro methane DCM. The polymorphic hGSTT1-1 may well play a role in the development of kidney tumours after high and long-term occupational exposure against trichloroethylene. Although several studies have investigated the association of this polymorphism with malignant diseases little is known about its enzyme activity in potential extrahepatic target tissues. The known theta-specific substrates methyl chloride (MC) dichloromethane and 1,2-epoxy-3-(p-nitrophenoxy)propane (EPNP) were used to assay GSTT1-1 activity in liver and kidney of rats, mice, hamsters and humans differentiating the three phenotypes (non-conjugators, low conjugators, high conjugators) seen in humans. In addition GSTT1-1 activity towards MC and DCM was determined in human erythrocytes. No GSTT1-1 activity was found in any tissue of non-conjugators (NC). In all organs high conjugators (HC) showed twofold higher activity towards MC and DCM than low conjugators (LC). The activity in human samples towards EPNP was too close to the detection limit to differentiate between the three conjugator phenotypes. GSTT1-1 activity towards MC was two to seven-times higher in liver cytosol than in kidney cytosol. The relation for MC between species was identical in both organs: mouse > HC > rat > LC > hamster > NC. In rats, mice and hamsters GSTT1-1 activity in liver cytosol towards DCM was also two to seven-times higher than in the kidney cytosol. In humans this activity was twice as high in kidney cytosol than in liver cytosol. The relation between species was mouse > rat > HC > LC > hamster > NC for liver, but mouse > HC > LC/rat > hamster/NC for kidney cytosol. The importance to heed the specific environment at potential target sites in risk assessment is emphasized by these results.
谷胱甘肽转移酶(GST)GSTT1-1参与多种工业广泛使用的化学物质的生物转化,如丁二烯和二氯甲烷(DCM)。多态性的人GSTT1-1很可能在长期高剂量职业接触三氯乙烯后肾肿瘤的发生中起作用。尽管有几项研究调查了这种多态性与恶性疾病的关联,但对其在潜在肝外靶组织中的酶活性知之甚少。已知的θ特异性底物氯甲烷(MC)、二氯甲烷和1,2-环氧-3-(对硝基苯氧基)丙烷(EPNP)被用于测定大鼠、小鼠、仓鼠和人类肝脏和肾脏中GSTT1-1的活性,区分人类中所见的三种表型(非结合者、低结合者、高结合者)。此外,还测定了人红细胞中GSTT1-1对MC和DCM的活性。在非结合者(NC)的任何组织中均未发现GSTT1-1活性。在所有器官中,高结合者(HC)对MC和DCM的活性比低结合者(LC)高两倍。人样品中对EPNP的活性过于接近检测限,无法区分三种结合者表型。GSTT1-1对MC的活性在肝细胞溶胶中比在肾细胞溶胶中高2至7倍。两个器官中MC的物种间关系相同:小鼠>HC>大鼠>LC>仓鼠>NC。在大鼠、小鼠和仓鼠中,肝细胞溶胶中GSTT1-1对DCM的活性也比肾细胞溶胶中高2至7倍。在人类中,这种活性在肾细胞溶胶中比在肝细胞溶胶中高两倍。肝脏的物种间关系为小鼠>大鼠>HC>LC>仓鼠>NC,但肾细胞溶胶的关系为小鼠>HC>LC/大鼠>仓鼠/NC。这些结果强调了在风险评估中注意潜在靶位点的特定环境的重要性。