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与癫痫持续状态相关的大鼠认知功能的品系间差异。

Interstrain differences in cognitive functions in rats in relation to status epilepticus.

作者信息

Hort J, Brozek G, Komárek V, Langmeier M, Mares P

机构信息

Department of Neurology, 2nd Medical School, Charles University, Prague, Czech Republic.

出版信息

Behav Brain Res. 2000 Jul;112(1-2):77-83. doi: 10.1016/s0166-4328(00)00163-7.

Abstract

Cognitive functions of Long Evans (N=30) and Wistar rats (N=32) were compared using a Morris water maze. Under control conditions the Long Evans rats were more efficient in this test, their average escape latency after 5 days of training (6.4+/-0.1 s, mean+/-S.E.M.) was significantly shorter than that of the Wistar rats (11.0+/-0.1 s). When the training was completed seizures were induced by an intraperitoneal injection of pilocarpine (330 mg/kg in the Long Evans strain and 350 mg/kg in the Wistar rats) 30 min after pretreatment with N-methylscopolamine (1 mg/kg i.p.). Clonazepam (1 mg/kg i.p.) was used to interrupt clonic seizures after 2 hours of continuous activity. Approximately one quarter of rats in both strains did not develop seizures. Severe convulsive status epilepticus was common in Long Evans rats (23 out of 30). In contrast, only 12 Wistar rats generated convulsive status epilepticus and the same number of animals exhibited only bursts of motor seizures separated by periods without convulsions (temporary seizures). Mortality after pilocarpine-induced status epilepticus was considerably higher in the Long Evans rats than in the Wistar rats. After a latency of 2-3 weeks spontaneous recurrent seizures appeared in all animals surviving status. Cognitive memory was tested during the 'silent period' between status and recurrent seizures. The Long Evans rats were unable to find the platform at the 3rd and 6th day after status but then their performance rapidly improved. The performance of the Wistar rats undergoing status epilepticus was seriously deteriorated and it never normalized, whereas the animals with temporary seizures exhibited only a transitory marginal prolongation of latencies. The hippocampal formation was damaged by status epilepticus in rats of both strains - the Long Evans rats exhibited more extensive damage of subfields CA1 and CA3, whereas in the Wistar rats a complete destruction of hilar neurons was observed in addition to partial CA1 and CA3 damage.

摘要

使用莫里斯水迷宫比较了长 Evans 大鼠(N = 30)和 Wistar 大鼠(N = 32)的认知功能。在对照条件下,长 Evans 大鼠在该测试中效率更高,训练 5 天后它们的平均逃避潜伏期(6.4±0.1 秒,平均值±标准误)明显短于 Wistar 大鼠(11.0±0.1 秒)。训练完成后,在用 N - 甲基东莨菪碱(1 毫克/千克腹腔注射)预处理 30 分钟后,通过腹腔注射匹鲁卡品(长 Evans 品系为 330 毫克/千克,Wistar 大鼠为 350 毫克/千克)诱导癫痫发作。持续活动 2 小时后,使用氯硝西泮(1 毫克/千克腹腔注射)中断阵挛性癫痫发作。两个品系中约四分之一的大鼠未发生癫痫发作。严重惊厥性癫痫持续状态在长 Evans 大鼠中很常见(30 只中有 23 只)。相比之下,只有 12 只 Wistar 大鼠产生惊厥性癫痫持续状态,相同数量的动物仅表现出由无惊厥期隔开的运动性癫痫发作阵发(暂时性癫痫发作)。匹鲁卡品诱导的癫痫持续状态后的死亡率在长 Evans 大鼠中比 Wistar 大鼠高得多。在癫痫持续状态和复发性癫痫发作之间的“静止期”对认知记忆进行了测试。长 Evans 大鼠在癫痫持续状态后的第 3 天和第 6 天无法找到平台,但随后它们的表现迅速改善。经历癫痫持续状态的 Wistar 大鼠的表现严重恶化且从未恢复正常,而有暂时性癫痫发作的动物仅表现出潜伏期的短暂轻微延长。两个品系大鼠的海马结构都因癫痫持续状态而受损——长 Evans 大鼠的 CA1 和 CA3 亚区损伤更广泛,而在 Wistar 大鼠中,除了 CA1 和 CA3 部分损伤外,还观察到门区神经元的完全破坏。

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