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海马体缺血会导致局部场电位和突触可塑性出现缺陷。

Hippocampal ischemia causes deficits in local field potential and synaptic plasticity.

作者信息

Wang Shaoli, Zhang Jingyun, Sheng Tao, Lu Wei, Miao Dengshun

机构信息

The Research Center for Bone and Stem Cells, Department of Human Anatomy.

The Key Laboratory of Developmental Genes and Human Disease, Institute of Life Sciences, Southeast University , Nanjing, Jiangsu 210096 , China.

出版信息

J Biomed Res. 2015 Sep;29(5):370-9. doi: 10.7555/JBR.29.20150010. Epub 2015 Jun 8.

Abstract

The long-term enhancement in glutamate receptor mediated excitatory responses has been observed in stroke model. This pathological form of plasticity, termed post-ischemic long-term potentiation (i-LTP), points to functional reorganization after stroke. Little is known, however, about whether and how this i-LTP would affect subsequent induction of synaptic plasticity. Here, we first directly confirmed that i-LTP was induced in the endothelin-1-induced ischemia model as in other in vitro models. We also demonstrated increased expression of NR2B, CaMKII and p-CaMKII, which are reminiscent of i-LTP. We further induced LTP of field excitatory postsynaptic potentials (fEPSPs) on CA1 hippocampal neurons in peri-infarct regions of the endothelin-1-induced mini-stroke model. We found that LTP of fEPSPs, induced by high-frequency stimulation, displayed a progressive impairment at 12 and 24 hours after ischemia. Moreover, using in vivo multi-channel recording, we found that the local field potential, which represents electrical property of cell ensembles in more restricted regions, was also dampened at these two time points. These results suggest that i-LTP elevates the induction threshold of subsequent synaptic plasticity. Our data helps to deepen the knowledge of meta-synaptic regulation of plasticity after focal ischemia.

摘要

在中风模型中已观察到谷氨酸受体介导的兴奋性反应的长期增强。这种可塑性的病理形式,称为缺血后长期增强(i-LTP),表明中风后存在功能重组。然而,关于这种i-LTP是否以及如何影响随后的突触可塑性诱导,人们知之甚少。在这里,我们首先直接证实,在内皮素-1诱导的缺血模型中,与其他体外模型一样,诱导了i-LTP。我们还证明了NR2B、CaMKII和p-CaMKII的表达增加,这让人联想到i-LTP。我们进一步在内皮素-1诱导的小中风模型的梗死周围区域的CA1海马神经元上诱导场兴奋性突触后电位(fEPSP)的LTP。我们发现,高频刺激诱导的fEPSP的LTP在缺血后12小时和24小时表现出逐渐受损。此外,使用体内多通道记录,我们发现代表更局限区域细胞集合电特性的局部场电位在这两个时间点也受到抑制。这些结果表明,i-LTP提高了随后突触可塑性的诱导阈值。我们的数据有助于加深对局灶性缺血后可塑性的元突触调节的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62bf/4585431/03a47c5489ea/jbr-29-05-370-g001a.jpg

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