Arivarasu N A, Fatima Sabiha, Mahmood Riaz
Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Aligarh 202002, UP, India.
Arch Toxicol. 2008 Dec;82(12):951-8. doi: 10.1007/s00204-008-0311-0. Epub 2008 May 17.
Potassium dichromate (K2Cr2O7) is a soluble hexavalent chromium compound that is widely used in several industries. In the present work the effect of administration of K2Cr2O7 on rat intestinal brush border membrane(BBM) enzymes and anti-oxidant system was studied. Rats were given a single oral dose of K2Cr2O7 (100 mg/kg bodyweight) and sacrificed 6, 12, 24, 48 and 96 h after the treatment.Control animals were not given K2Cr2O7. The administration of K2Cr2O7 resulted in a reversible decline in the specific activities of several BBM enzymes. The decrease in the activities of these enzymes was due to changes in the maximum velocity while their affinities for the substrates remained unchanged. Lipid peroxidation increased while total SH groups decreased in K2Cr2O7-treated rats as compared to controls indicating increased oxidative stress in the intestinal mucosa. The activities of superoxide dismutase and glutathione-S-transferase increased while those of catalase, glutathione reductase, thioredoxin reductase and glucose-6-phosphate dehydrogenase decreased. The maximum changes in all the parameters studied above were 24 h after administration of K2Cr2O7 after which recovery took place,in most cases almost to control values after 96 h. These results show that oral administration of K2Cr2O7 to decrease in the activities of BBM enzymes, increase in oxidative stress and alters the activities of anti-oxidant enzymes in rat intestine.
重铬酸钾(K2Cr2O7)是一种可溶性六价铬化合物,广泛应用于多个行业。在本研究中,研究了给予K2Cr2O7对大鼠肠刷状缘膜(BBM)酶和抗氧化系统的影响。给大鼠单次口服K2Cr2O7(100mg/kg体重),并在处理后6、12、24、48和96小时处死。对照动物未给予K2Cr2O7。给予K2Cr2O7导致几种BBM酶的比活性可逆下降。这些酶活性的降低是由于最大速度的变化,而它们对底物的亲和力保持不变。与对照组相比,K2Cr2O7处理的大鼠脂质过氧化增加,总SH基团减少,表明肠黏膜氧化应激增加。超氧化物歧化酶和谷胱甘肽-S-转移酶的活性增加,而过氧化氢酶、谷胱甘肽还原酶、硫氧还蛋白还原酶和葡萄糖-6-磷酸脱氢酶的活性降低。上述所有参数的最大变化发生在给予K2Cr2O7后24小时,之后开始恢复,在大多数情况下,96小时后几乎恢复到对照值。这些结果表明,口服K2Cr2O7会导致大鼠肠中BBM酶活性降低、氧化应激增加并改变抗氧化酶的活性。