首页> 外文期刊>Epilepsy research >Different effects of neuroprotectants FK-506 and cyclosporin A on susceptibility to pilocarpine-induced seizures in rats with brain injured at different developmental stages.
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Different effects of neuroprotectants FK-506 and cyclosporin A on susceptibility to pilocarpine-induced seizures in rats with brain injured at different developmental stages.

机译:神经保护剂FK-506和环孢菌素A对不同发育阶段脑损伤大鼠对毛果芸香碱引起的癫痫发作敏感性的不同影响。

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Susceptibility of the injured brain to epileptic seizures depends on the developmental stage at which the injury had been inflicted (our previous paper published in Epilepsy Res. 53 (2003) 216-224). The present study was designed to examine whether neuroprotective agents applied following the injury can decrease the seizure susceptibility. In order to solve this problem, the left cerebral hemisphere was mechanically injured in 6- and 30-day-old Wistar rats. Neuroprotectants FK506 or Cyclosporin A (CsA) were injected 20min and 24h following the injury. On postnatal day 60, all the animals received single i.p. pilocarpine injections to evoke epileptic seizures. During a 6h period following the injection, the animals were observed continuously and pilocarpine-induced symptoms were recorded and rated. The animals were sacrificed 7 days after pilocarpine injection. In rats injured on postnatal days 6 or 30 (P6 or P30, respectively) and injected with FK-506 after the injury, signs of amelioration in the course of epilepsy were observed. Generally, proportions of rats suffering from heavy seizures were lower and/or their survival periods were longer. Following treatment with CsA, proportions of rats displaying heavy seizures were greater. It was accompanied by extremely high mortality (in rats injured on P6) or a longer duration of seizures (in rats injured on P30). The results appear to point to age-dependent differences between the mechanisms of action of the two neuroprotectants.
机译:受伤的大脑对癫痫发作的易感性取决于造成伤害的发育阶段(我们先前的论文发表在Epilepsy Res。53(2003)216-224)。本研究旨在检查损伤后应用神经保护剂是否可以降低癫痫发作的易感性。为了解决这个问题,在6日龄和30日龄的Wistar大鼠中,左大脑半球受到机械损伤。损伤后20分钟和24小时注射神经保护剂FK506或环孢菌素A(CsA)。在出生后第60天,所有动物均接受单次腹腔注射。毛果芸香碱注射液引起癫痫发作。在注射后6小时内,连续观察动物并记录和评估毛果芸香碱引起的症状。毛果芸香碱注射后7天处死动物。在出生后第6天或第30天(分别为P6或P30)受伤并在受伤后注射FK-506的大鼠中,观察到癫痫发作过程中症状有所改善。通常,患有严重癫痫的大鼠比例较低和/或它们的生存期较长。用CsA治疗后,表现出严重癫痫发作的大鼠比例更大。它伴随着极高的死亡率(在P6受伤的大鼠中)或更长的癫痫发作持续时间(在P30受伤的大鼠中)。结果似乎表明两种神经保护剂作用机制之间的年龄依赖性差异。

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