...
首页> 外文期刊>Archives of Toxicology >Oral administration of potassium dichromate inhibits brush border membrane enzymes and alters anti-oxidant status of rat intestine
【24h】

Oral administration of potassium dichromate inhibits brush border membrane enzymes and alters anti-oxidant status of rat intestine

机译:口服重铬酸钾抑制大鼠刷状缘膜酶并改变大鼠肠的抗氧化状态

获取原文
获取原文并翻译 | 示例

摘要

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 body weight) 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.
机译:重铬酸钾(K2 Cr2 O7 )是一种可溶性六价铬化合物,已在多个行业中广泛使用。在本工作中,研究了施用K2 Cr2 O7 对大鼠肠刷状缘膜(BBM)酶和抗氧化系统的影响。给大鼠口服单剂量的K2 Cr2 O7 (100 mg / kg体重),并在治疗后6、12、24、48和96 h处死。对照动物未给予K2 Cr2 O7 。施用K2 Cr2 O7 导致几种BBM酶的比活性可逆地下降。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却保持不变。与对照组相比,K2 2 O7 处理的大鼠脂质过氧化增加,而总SH组减少,表明肠粘膜氧化应激增加。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6-磷酸葡萄糖脱氢酶的活性降低。以上研究的所有参数的最大变化是在施用K2 2 O7 后的24小时内发生的,恢复后,在大多数情况下96小时后几乎恢复到控制值。这些结果表明,口服K2 Cr2 O7 可以降低大鼠肠内BBM酶的活性,增加氧化应激并改变其抗氧化酶的活性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号