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首页> 外文期刊>Brain research >The role of superoxide dismutase and alpha-tocopherol in the development of seizures and kindling induced by pentylenetetrazol - influence of the radical scavenger alpha-phenyl-N-tert-butyl nitrone.
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The role of superoxide dismutase and alpha-tocopherol in the development of seizures and kindling induced by pentylenetetrazol - influence of the radical scavenger alpha-phenyl-N-tert-butyl nitrone.

机译:超氧化物歧化酶和α-生育酚在戊四氮诱发的癫痫发作和点燃中的作用-自由基清除剂α-苯基-N-叔丁基硝酮的影响。

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摘要

Previous experiments have shown that the generation of free hydroxyl radicals in rat brain homogenates is increased following pentylenetetrazol (PTZ) kindling. The present study was performed in order to evaluate the involvement of endogeneous radical defence systems as the superoxide dismutase (SOD) and the level of alpha-tocopherol, an important lipid-soluble and membrane-bound antioxidant in brain homogenate of rats after acute seizure and kindling induced by PTZ. The activities of the total SOD were significantly reduced after acute seizure and tend towards an enhancement in kindled animals. Western blot analysis shows an upregulation of Mn-SOD in rat brain homogenates after kindling. The level of the chain-breaking antioxidant alpha-tocopherol was reduced in acutely convulsing rats and was not modified in kindled rats. Second, we studied the influence of exogeneously supplied radical scavenger alpha-phenyl-N-tert-butyl-nitrone (PBN) on seizure and kindling following PTZ treatment. After a single injection of PTZ at a dose evoking clonic-tonic seizures, PBN did not modify either the formation of free hydroxyl radicals measured by the levels of 2,3-dihydroxybenzoic acid (DHBA) and 2,5-DHBA or the susceptibility to PTZ. In the kindling group, subchronic treatment with PBN (over a period of 4 weeks) prevented the increase in the formation of free hydroxyl radicals, and the susceptibility to PTZ was transiently decreased during the development of kindling, but PBN did not influence the susceptibility to PTZ in fully kindled rats. Pretreatment with PBN increased the activities of total SOD and the protein content of Mn-SOD and decreased the level of alpha-tocopherol in comparison to saline controls. The results suggest that the formation of free hydroxyl radicals is not reflected by an enhanced susceptibility to PTZ classified according to the modified RACINE scale. Additionally, it may be assumed that the increased generation of hydroxyl radicals in kindled animals is not primary caused by an exhaustion of both the defence systems measured. Adaptive mechanisms, as the induction of Mn-SOD, may be taken into consideration to counteract oxidative stress-mediated free radical formation.
机译:先前的实验表明,在戊四氮(PTZ)点燃后,大鼠脑匀浆中游离羟基的产生增加。进行本研究是为了评估内源性自由基防御系统作为超氧化物歧化酶(SOD)和α-生育酚的水平的参与,α-生育酚是急性癫痫发作后大鼠脑匀浆中重要的脂溶性和膜结合性抗氧化剂。由PTZ引发。急性癫痫发作后,总SOD的活性显着降低,并趋向增强。蛋白质印迹分析显示,点燃后大鼠脑匀浆中的Mn-SOD上调。在急性惊厥大鼠中,链断裂抗氧化剂α-生育酚的水平降低,而在点燃大鼠中并未改变。其次,我们研究了外源提供的自由基清除剂α-苯基-N-叔丁基-硝基(PBN)对PTZ处理后癫痫发作和点燃的影响。在单剂量注射PTZ引起阵挛性癫痫发作后,PBN不会改变通过2,3-二羟基苯甲酸(DHBA)和2,5-DHBA的水平测量的游离羟基自由基的形成或对云台。在点燃组中,PBN亚慢性治疗(4周以上)可防止游离羟基自由基的形成增加,并且在点燃过程中对PTZ的敏感性会暂时降低,但PBN不会影响对PTZ的敏感性。完全点燃的大鼠中的PTZ。与盐水对照组相比,PBN预处理可增加总SOD活性和Mn-SOD的蛋白质含量,并降低α-生育酚的水平。结果表明,根据修改后的RACINE等级对PTZ的敏感性增强并未反映出游离羟基的形成。另外,可以假设,被点燃的动物体内羟基自由基产生的增加并不是由所测量的两种防御系统都耗尽引起的。可以考虑将自适应机制作为Mn-SOD的诱导来抵消氧化应激介导的自由基形成。

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