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高频刺激海马可预防猴体内海人酸诱导的癫痫发作活动和海马神经元凋亡。

High-frequency stimulation of the hippocampus protects against seizure activity and hippocampal neuronal apoptosis induced by kainic acid administration in macaques.

机构信息

Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.

Department of Neurology, The Sixth People Hospital of Jinan, Jinan, China.

出版信息

Neuroscience. 2014 Jan 3;256:370-8. doi: 10.1016/j.neuroscience.2013.10.059. Epub 2013 Nov 4.

Abstract

Kainic acid (KA) administration is known to cause seizures and neuronal death in the hippocampus. High-frequency stimulation (HFS) of the hippocampus can be a promising method in the treatment of epilepsy while the mechanism of action is unknown yet. It remains unknown whether HFS is neuroprotective for hippocampal neurons following KA-induced seizures in macaques, although HFS has neuroprotective effects in animal models of Parkinson's disease. We therefore examined the effects of HFS on KA-induced seizures and neuronal survival in macaque's hippocampus. Seizure frequency following KA that led to seizures in macaques was strongly reduced by HFS of the hippocampus. In addition, administration of KA led to marked neuronal apoptosis in the hippocampus, accompanied by increased levels of Bax, activated caspase-3 and decreased levels of Bcl-2. HFS was found to attenuate changes in apoptosis-related proteins and robustly decreased neuronal loss following KA administration. These data indicate that hippocampal HFS can protect hippocampal neurons against KA neurotoxicity, and that HFS neuroprotection is likely to operate with inhibition of apoptosis.

摘要

海人酸(KA)给药已知会在海马体中引起癫痫发作和神经元死亡。海马体的高频刺激(HFS)可能是治疗癫痫的一种很有前途的方法,但其作用机制尚不清楚。尽管 HFS 在帕金森病动物模型中具有神经保护作用,但 HFS 是否对猴 KA 诱导的癫痫发作后的海马神经元具有神经保护作用仍不清楚。因此,我们研究了 HFS 对猴海马体中 KA 诱导的癫痫发作和神经元存活的影响。海马体 HFS 强烈降低了导致猴癫痫发作的 KA 后的癫痫发作频率。此外,KA 的给药导致海马体中明显的神经元细胞凋亡,同时 Bax 水平升高,活化的 caspase-3 增加,Bcl-2 减少。研究发现 HFS 可减轻与凋亡相关的蛋白质的变化,并在 KA 给药后显著减少神经元丢失。这些数据表明,海马体 HFS 可以保护海马神经元免受 KA 的神经毒性,并且 HFS 的神经保护作用可能通过抑制细胞凋亡来实现。

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