Sparrow S, Magos L, Snowden R
Life Science Research, Elm Farm Laboratories Occold, Nr. Eye, Suffolk, United Kingdom.
Arch Toxicol. 1988;61(6):440-3. doi: 10.1007/BF00293689.
Sodium chromate (20 mg/kg, s.c.), which in male rats inflicted necrotic damage mainly in the P1 region (proximal part of the proximal convoluted tubules), protected against proximal tubular necrosis induced by 0.5 or 3.0 mg Hg2+/kg in the P2 (distal part of the proximal convoluted tubules) and P3 (pars recta part of the proximal tubules) regions. Histochemical staining for mercury indicated that chromate increased mercury deposition in those cells of the P1 region which were unaffected by chromate (had intact brush border) but did not decrease mercury deposition in the most severely affected P3 region. Chromate pretreatment actually increased mercury deposition in the kidneys of animals killed 24 h after the injection of 0.5 mg Hg2+. The protective effect was mutual. Cellular proliferation and fibrosis observed 4-5 days after chromate were prevented by injecting 0.5 mg Hg2+/kg 3 days after chromate treatment.
铬酸钠(20毫克/千克,皮下注射)在雄性大鼠中主要造成P1区域(近端曲管近端部分)的坏死损伤,可预防由0.5或3.0毫克汞离子/千克引起的P2(近端曲管远端部分)和P3(近端小管直部)区域的近端肾小管坏死。汞的组织化学染色表明,铬酸盐增加了P1区域未受铬酸盐影响(刷状缘完整)的细胞中的汞沉积,但并未减少受影响最严重的P3区域中的汞沉积。铬酸盐预处理实际上增加了注射0.5毫克汞离子后24小时处死的动物肾脏中的汞沉积。这种保护作用是相互的。在铬酸盐处理3天后注射0.5毫克汞离子/千克,可预防铬酸盐处理后4 - 5天观察到的细胞增殖和纤维化。