Iscan M, Coban T, Eke B C
Department of Toxicology, Faculty of Pharmacy, Ankara University, Tandogan, Turkey.
Environ Health Perspect. 1994 Nov;102 Suppl 9(Suppl 9):69-72. doi: 10.1289/ehp.94102s969.
When male guinea pigs were given a single dose of Cd (2.0 mg Cd2+/kg, ip) 72 hr prior to sacrifice, the hepatic reduced glutathione (GSH) level did not change although glutathione S-transferase (GST) activities toward the substrates 1-chloro-2,4-dinitrobenzene (CDNB), 1,2-dichloro-4-nitrobenzene (DCNB), ethacrynic acid (EAA), and 1,2-epoxy-3-(p-nitrophenoxy) propane (ENPP) increased significantly as compared to controls. Cd did not change the renal GSH level and GST activities toward CDNB and EAA. However, significant increase was observed in the GST activity for DCNB whereas GST activity for ENPP was significantly inhibited by Cd. When the animals were given a single dose of Ni (14.8 mg Ni2+/kg, sc) 16 hr prior to sacrifice, significant increases were observed in hepatic GSH level and GST activities toward CDNB, DCNB, EAA and ENPP. Ni, however, depressed the renal GSH level and GST activities toward CDNB, DCNB and ENPP significantly. The renal GST activity toward EAA remained unaltered. For the combined treatment, guinea pigs received the single dose of Ni 56 hr after the single dose of Cd and then they were killed 16 hr later. In these animals, no significant alteration was observed in the hepatic GSH level. The augmentation of elevation was observed in hepatic GST activities toward CDNB and DCNB. Combined metal treatment did not potentiate the elevation of hepatic GST activities toward EAA and ENPP to any greater degree. The depression of renal GSH level was significantly ameliorated by the combined treatment. Combination treatment potentiated the depression of renal GST activity for ENPP but not for CDNB.(ABSTRACT TRUNCATED AT 250 WORDS)
在处死雄性豚鼠前72小时,给其腹腔注射单剂量的镉(2.0毫克Cd2 + /千克),尽管谷胱甘肽S - 转移酶(GST)对底物1 - 氯 - 2,4 - 二硝基苯(CDNB)、1,2 - 二氯 - 4 - 硝基苯(DCNB)、依他尼酸(EAA)和1,2 - 环氧 - 3 -(对硝基苯氧基)丙烷(ENPP)的活性与对照组相比显著增加,但肝脏中还原型谷胱甘肽(GSH)水平未发生变化。镉未改变肾脏GSH水平以及GST对CDNB和EAA的活性。然而,观察到GST对DCNB的活性显著增加,而镉显著抑制了GST对ENPP的活性。在处死动物前16小时,给其皮下注射单剂量的镍(14.8毫克Ni2 + /千克),观察到肝脏GSH水平以及GST对CDNB、DCNB、EAA和ENPP的活性显著增加。然而,镍显著降低了肾脏GSH水平以及GST对CDNB、DCNB和ENPP的活性。肾脏GST对EAA的活性保持不变。对于联合治疗,豚鼠在注射单剂量镉56小时后接受单剂量镍注射,然后在16小时后处死。在这些动物中,肝脏GSH水平未观察到显著变化。观察到肝脏GST对CDNB和DCNB的活性增强。联合金属处理并未使肝脏GST对EAA和ENPP的活性升高到更大程度。联合治疗显著改善了肾脏GSH水平的降低。联合治疗增强了肾脏GST对ENPP的活性降低,但对CDNB没有影响。(摘要截选至250字)