Kim S G, Nam S Y, Kim C W, Cho C K, Kim N D
College of Pharmacy, Duksung Women's University, Seoul, South Korea.
Res Commun Mol Pathol Pharmacol. 1998 Sep;101(3):275-88.
2-(Allylthio)pyrazine (2-AP), which is effective in suppressing constitutive and inducible cytochrome P450 2E1 expression, exhibits hepatoprotective and chemopreventive effects. The radioprotective effects of 2-AP were examined in animals in association with the expression of microsomal epoxide hydrolase (mEH) and glutathione S-transferases (GSTs). 2-AP pretreatment (100 mg/kg/day, for 2 days) prior to total body irradiation (TBI) at the dose of 8 Gy increased the 30 day survival rate of mice to 91% from 48% in TBI alone. 2-AP caused an increase in the mean survival time of mice exposed to 9 Gy of TBI. Light microscopic examinations revealed that exposure of mice to 8 Gy of gamma-ray radiation resulted in hepatocyte degeneration in the surviving animals at day 1 through day 22 with certain extents of necrosis observed at early times, whereas 2-AP pretreatment protected the liver against ionizing radiation with no hepatic necrosis being observed. Mice irradiated at the dose of 8 Gy showed time-related decreases in the counts of WBC, RBC and platelet. 2-AP treatment, however, failed to protect the peripheral blood cells against gamma-irradiation and resulted in no improvement in the ratio of myeloid to erythroid bone marrow cells, as compared to TBI alone. Northern blot analysis revealed that exposure of mice to 8 Gy of TBI plus 2-AP exhibited greater mEH and mGSTA3 mRNA levels in the liver than those with TBI alone, although mGSTP1 mRNA level failed to be altered. Studies were also extended to determine the effects of 0.5 Gy gamma-irradiation in combination with 2-AP on the expression of hepatic mEH and GST genes in rats. Whereas mEH, rGSTA2, rGSTA3 and rGSTA5 mRNA levels were elevated 2- to 2.8-fold at 24 h after 2-AP treatment at the dose of 30 mg/kg, rats exposed to both 2-AP and 0.5 Gy of irradiation showed greater relative increases in the mRNAs. 2-AP enhanced the mEH and rGSTA2 gene expression to greater extents at day 1 after irradiation than after 3-5 consecutive daily treatment. The radiation-inducible mRNA levels of rGSTA3/5 and rGSTM1/2 were affected less by 2-AP pretreatment than were those of mEH and rGSTA2. These results demonstrate that 2-AP exhibits radioprotective efficacy against gamma-ray ionizing radiation in both mice and rats, which might be associated with enhanced expression of mEH and GST genes, but not with hematological improvement.
2-(烯丙硫基)吡嗪(2-AP)可有效抑制组成型和诱导型细胞色素P450 2E1的表达,具有肝脏保护和化学预防作用。本研究结合微粒体环氧化物水解酶(mEH)和谷胱甘肽S-转移酶(GSTs)的表达,检测了2-AP对动物的辐射防护作用。全身照射(TBI)剂量为8 Gy前,给予2-AP预处理(100 mg/kg/天,共2天),可使小鼠30天生存率从单纯TBI组的48%提高至91%。2-AP可延长接受9 Gy TBI照射小鼠的平均生存时间。光学显微镜检查显示,接受8 Gy γ射线照射的小鼠,在第1天至第22天存活动物中出现肝细胞变性,早期可见一定程度的坏死,而2-AP预处理可保护肝脏免受电离辐射,未观察到肝坏死。接受8 Gy照射的小鼠,白细胞、红细胞和血小板计数呈时间依赖性下降。然而,与单纯TBI组相比,2-AP治疗未能保护外周血细胞免受γ射线照射,也未改善骨髓细胞中髓系与红系的比例。Northern印迹分析显示,接受8 Gy TBI加2-AP照射的小鼠肝脏中,mEH和mGSTA3 mRNA水平高于单纯TBI组,而mGSTP1 mRNA水平未改变。研究还扩展至检测0.5 Gy γ射线照射联合2-AP对大鼠肝脏mEH和GST基因表达的影响。给予30 mg/kg剂量的2-AP处理24小时后,mEH、rGSTA2、rGSTA3和rGSTA5 mRNA水平升高2至2.8倍,同时接受2-AP和0.5 Gy照射的大鼠,mRNA相对增加幅度更大。与连续每日处理3至5天相比,2-AP在照射后第1天对mEH和rGSTA2基因表达的增强作用更大。2-AP预处理对rGSTA3/5和rGSTM1/2辐射诱导的mRNA水平的影响小于mEH和rGSTA2。这些结果表明,2-AP对小鼠和大鼠的γ射线电离辐射均具有辐射防护作用,这可能与mEH和GST基因表达增强有关,但与血液学改善无关。