Wu S L, Qin X, Guo S C
Department of Phylaxiology, Xiamen Medical College, Xiamen 361023, China.
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2017 Feb 20;35(2):91-95. doi: 10.3760/cma.j.issn.1001-9391.2017.02.003.
To elucidate the effect of taurine on neurotoxicity induced by Mn by investigating activities of Na(+)-K(+)-ATPase and Ca(2+)-Mg(2+)-ATPase and content of Mn and active calmodulin in manganese exposed rats. 156 male SD rats were randomly divided into 1 control group, 3 manganese exposed groups (10, 15, and 20 mg/kg respectively) , and 9 taurine intervened groups based on orthogonal design (doses of taurine intervention were 100, 150, and 200 mg/kg respectively) , with 12 rats in each group. After 12 weeks of exposure, all rats were decapitated and corpus striatums were removed, activities of Na(+)-K(+)-ATPase and Ca(2+)-Mg(2+)-ATPase and content of Mn and active calmodulin were analyzed. The corpus striatum Mn content of the 3 dose groups exposed to Mn and 9 taurine intervened groups were significantly higher than that of the control group (<0.05) . Active calmodulin content in 10 mg/kg manganese exposed group was significantly higher than that of the control group (<0.05) . 150 and 200 mg/kg of taurine could decrease active calmodulin content of the group exposed to 10 mg/kg of Mn (<0.05) . The corpus striatum activities of Na(+)-K(+)-ATPase and Ca(2+)-Mg(2+)-ATPase of the 3 dose groups exposed to Mn were significantly lower than that of the control group (<0.05) . 150 mg/kg of taurine could increase activities of Na(+)-K(+)-ATPase of the group exposed to 10 mg/kg of Mn (<0.05) . 150 and 200 mg/kg of taurine could respectively improve activities of Ca(2+)-Mg(2+)-ATPase of the group exposed to 15, 10 mg/kg of Mn (<0.05) . Mn can decrease the rats corpus striatum activities of Na(+)-K(+)-ATPase and Ca(2+)-Mg(2+)-ATPase, effect level of active calmodulin in relation to dose of Mn, to a certain extent, taurine could regulate activities of Na(+)-K(+)-ATPase and Ca(2+)-Mg(2+)-ATPase and improve the level of active calmodulin.
通过研究锰暴露大鼠的钠钾ATP酶、钙镁ATP酶活性以及锰和活性钙调蛋白含量,以阐明牛磺酸对锰诱导的神经毒性的影响。将156只雄性SD大鼠随机分为1个对照组、3个锰暴露组(分别为10、15和20mg/kg)和9个基于正交设计的牛磺酸干预组(牛磺酸干预剂量分别为100、150和200mg/kg),每组12只大鼠。暴露12周后,断头处死所有大鼠并取出纹状体,分析钠钾ATP酶、钙镁ATP酶活性以及锰和活性钙调蛋白含量。3个锰暴露剂量组和9个牛磺酸干预组的纹状体锰含量均显著高于对照组(<0.05)。10mg/kg锰暴露组的活性钙调蛋白含量显著高于对照组(<0.05)。150和200mg/kg牛磺酸可降低10mg/kg锰暴露组的活性钙调蛋白含量(<0.05)。3个锰暴露剂量组的纹状体钠钾ATP酶和钙镁ATP酶活性均显著低于对照组(<0.05)。150mg/kg牛磺酸可提高10mg/kg锰暴露组的钠钾ATP酶活性(<0.05)。150和200mg/kg牛磺酸可分别提高15、10mg/kg锰暴露组的钙镁ATP酶活性(<0.05)。锰可降低大鼠纹状体钠钾ATP酶和钙镁ATP酶活性,活性钙调蛋白受锰剂量影响,一定程度上牛磺酸可调节钠钾ATP酶和钙镁ATP酶活性并改善活性钙调蛋白水平。