Suppr超能文献

能量底物可保护清醒大鼠海马免受内源性谷氨酸介导的神经退行性变。

Energy substrates protect hippocampus against endogenous glutamate-mediated neurodegeneration in awake rats.

作者信息

Netzahualcoyotzi Citlalli, Tapia Ricardo

机构信息

División de Neurociencias, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, AP 70-253, 04510, Mexico, DF, Mexico.

出版信息

Neurochem Res. 2014 Jul;39(7):1346-54. doi: 10.1007/s11064-014-1318-y. Epub 2014 May 1.

Abstract

Excitotoxicity due to excessive glutamatergic neurotransmission is a well-studied phenomenon that has been related to the mechanisms of neuronal death occurring in some disorders of the CNS. We have previously shown that the intrahippocampal perfusion by microdialysis of 4-aminopyridine (4-AP) in rats stimulates endogenous glutamate release from nerve endings and this results in excitotoxic effects such as immediate seizures and delayed neuronal death, due to the overactivation of N-methyl-D-aspartate (NMDA) receptors. To study whether mitochondrial energy dysfunction and oxidative stress could be involved in this 4-AP-induced excitotoxicity, we evaluated in awake rats the protective effect of several energy substrates and antioxidant compounds, using microdialysis, electroencephalographic (EEG) recording and histological analysis. The 4-AP-induced behavioral and EEG seizures, which progressed to status epilepticus in about 30 min, were prevented by the NMDA receptor antagonist MK-801, whereas acetoacetate, DL- and L-β-hydroxybutyrate did not protect against seizures but increased the latency to the onset of status epilepticus; pyruvate, α-ketoglutarate and glutathione ethyl ester did not show any protective effect. 4-AP also produced nearly complete loss of pyramidal neurons in CA1 and CA3 regions of the ipsilateral hippocampus 24 h after the experiment. MK-801 totally prevented this neuronal death and the energy substrates tested protected by about 50%, whereas the antioxidants showed only a weak protection. We conclude that ketone bodies possess weak anticonvulsant effects and that energy metabolism impairment plays a more important role than oxidative stress in the delayed hippocampal neurodegeneration resulting from the excitotoxic action of 4-AP mediated by endogenous glutamate.

摘要

由于谷氨酸能神经传递过度导致的兴奋毒性是一种经过充分研究的现象,它与中枢神经系统某些疾病中发生的神经元死亡机制有关。我们之前已经表明,通过微透析向大鼠海马内灌注4-氨基吡啶(4-AP)会刺激神经末梢释放内源性谷氨酸,这会导致兴奋毒性效应,如立即发作癫痫和延迟性神经元死亡,这是由于N-甲基-D-天冬氨酸(NMDA)受体过度激活所致。为了研究线粒体能量功能障碍和氧化应激是否可能参与这种4-AP诱导的兴奋毒性,我们使用微透析、脑电图(EEG)记录和组织学分析,在清醒大鼠中评估了几种能量底物和抗氧化化合物的保护作用。4-AP诱导的行为和EEG癫痫发作在约30分钟内进展为癫痫持续状态,NMDA受体拮抗剂MK-801可预防这种情况,而乙酰乙酸、DL-和L-β-羟基丁酸不能预防癫痫发作,但可增加癫痫持续状态发作的潜伏期;丙酮酸、α-酮戊二酸和谷胱甘肽乙酯未显示出任何保护作用。实验24小时后,4-AP还导致同侧海马CA1和CA3区域的锥体神经元几乎完全丧失。MK-801完全预防了这种神经元死亡,所测试的能量底物提供了约50%的保护,而抗氧化剂仅显示出微弱的保护作用。我们得出结论,酮体具有微弱的抗惊厥作用,并且在由内源性谷氨酸介导的4-AP兴奋毒性作用导致的延迟性海马神经退行性变中,能量代谢损害比氧化应激起更重要的作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验