Sagai M, Ichinose T
Research Team for Health Effects of Air Pollutants, National Institute for Environmental Studies, Ibaraki, Japan.
Toxicology. 1991 Feb;66(2):121-32. doi: 10.1016/0300-483x(91)90213-k.
Lipid peroxide production, antioxidant contents and activities of antioxidative protective enzymes were examined in lungs of rats exposed to clean air (control group), 0.05 ppm O3, 0.05 ppm O3 + 0.04 ppm NO2 and 0.05 ppm O3 + 0.4 ppm NO2 for 22 months. The results were compared with our previous data in rats exposed to 0.04 ppm NO2, 0.4 ppm NO2 and 4 ppm NO2 for their life span (Sagai et al., Toxicol. Appl. Pharmacol., 73, (1984) 444-456). TBA values used as an index of lipid peroxidation in the lungs were increased maximally at 9 months, but were decreased below control values in animals exposed for 18 and 22 months. Nonprotein sulfhydryl (NPSH) contents were increased maximally at 9 months, and after 18 and 22 months were decreased significantly below control values. Vitamin E (VE) contents showed a similar trend. On the other hand, enzyme activities of glucose-6-phosphate dehydrogenase (G6PD), 6-phosphogluconate dehydrogenase (6PGD), glutathione reductase (GR), glutathione peroxidase measured by using cumene hydroperoxide (cum.OOH) substrate (GPx-cum.OOH), glutathione peroxidase measured by using H2O2 as a substrate (GPx-H2O2), glutathione S-transferase (GSH-Tase) and superoxide dismutase (SOD) did not show any significant changes during this experiment. The results show that lipid peroxidation in lungs was increased synergistically by a combination of NO2 and O3 at ambient levels, and that the time of maximum lipid peroxide production was shorter than with NO2 alone. The protective ability against lipid peroxides was higher with increased lipid peroxide levels, but the inducibility was not maintained through a life span exposure to the combined gases. Additionally, two small adenomas were observed in 2 out of 18 rats in the 0.05 ppm O3 + 0.04 ppm NO2 group and a large adenoma was observed in 1 out of 18 animals in the 0.05 ppm + 0.4 ppm NO2 group exposed for 22 months.
检测了暴露于清洁空气(对照组)、0.05 ppm 臭氧、0.05 ppm 臭氧 + 0.04 ppm 二氧化氮以及 0.05 ppm 臭氧 + 0.4 ppm 二氧化氮环境中 22 个月的大鼠肺组织中脂质过氧化物的产生、抗氧化剂含量以及抗氧化保护酶的活性。将这些结果与我们之前关于终生暴露于 0.04 ppm 二氧化氮、0.4 ppm 二氧化氮和 4 ppm 二氧化氮环境中的大鼠的数据进行了比较(Sagai 等人,《毒理学与应用药理学》,73 卷,(1984) 444 - 456 页)。用作肺组织脂质过氧化指标的硫代巴比妥酸(TBA)值在 9 个月时最大程度升高,但在暴露 18 个月和 22 个月的动物中降至对照值以下。非蛋白巯基(NPSH)含量在 9 个月时最大程度升高,在 18 个月和 22 个月后显著降至对照值以下。维生素 E(VE)含量呈现类似趋势。另一方面,在本实验期间,葡萄糖 - 6 - 磷酸脱氢酶(G6PD)、6 - 磷酸葡萄糖酸脱氢酶(6PGD)、谷胱甘肽还原酶(GR)、使用氢过氧化异丙苯(cum.OOH)底物测定的谷胱甘肽过氧化物酶(GPx - cum.OOH)、使用过氧化氢作为底物测定的谷胱甘肽过氧化物酶(GPx - H2O2)、谷胱甘肽 S - 转移酶(GSH - Tase)和超氧化物歧化酶(SOD)的酶活性未显示任何显著变化。结果表明,在环境水平下,二氧化氮和臭氧联合作用可协同增加肺组织中的脂质过氧化,并且脂质过氧化物产生的最大值出现时间比单独暴露于二氧化氮时短。随着脂质过氧化物水平升高,对脂质过氧化物的保护能力增强,但在终生暴露于混合气体的情况下,诱导能力无法维持。此外,在暴露 22 个月的 0.05 ppm 臭氧 + 0.04 ppm 二氧化氮组的 18 只大鼠中有 2 只观察到两个小腺瘤,在 0.05 ppm + 0.4 ppm 二氧化氮组的 18 只动物中有 1 只观察到一个大腺瘤。