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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >ACTIVATION OF INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS DURING PRECONDITIONING LOW-FREQUENCY STIMULATION SUPPRESSES SUBSEQUENT INDUCTION OF LONG-TERM POTENTIATION IN HIPPOCAMPAL CA1 NEURONS
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ACTIVATION OF INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS DURING PRECONDITIONING LOW-FREQUENCY STIMULATION SUPPRESSES SUBSEQUENT INDUCTION OF LONG-TERM POTENTIATION IN HIPPOCAMPAL CA1 NEURONS

机译:预处理低频刺激过程中肌苷1,4,5-三磷酸受体的激活抑制了海马CA1神经元长期诱导的继发性

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We investigated the role of inositol 1,4,5-trisphosphate receptors (IP(3)Rs) activated during preconditioning low-frequency stimulation (LFS) in the subsequent high-frequency stimulation (HFS)-induced induction of long-term potentiation (LTP) in CA1 neurons in hippocampal slices from mature guinea pigs. Induction of LTP in the field excitatory postsynaptic potential (EPSP) or the population spike (PS) by delivery of HFS (a tetanus of 100 pulses at 100 Hz) to the Schaffer collateral-commissural pathway to CA1 neuron synapses was suppressed when the CA1 synapses were preconditioned by LFS of 1000 pulses at 1 Hz. This effect was inhibited when the preconditioning LFS was applied in the presence of an N-methyl-D-aspartate receptors (NMDARs) antagonist, a metabotropic glutamate receptor (mGluR) antagonist, IP3R antagonist, a calmodulin-dependent kinase II inhibitor or a calcineurin inhibitor. Furthermore, blockade of group I mGluRs immediately before the delivery of HFS blocked the inhibitory effect of the preconditioning LFS on subsequent induction of LTP by HFS. These results suggest that, in hippocampal CA1 neuron synapses, co-activation of NMDARs and IP(3)Rs during a preconditioning LFS results in both phosphorylation and dephosphorylation events that lead to prolonged activation of group I mGluRs that is responsible for the failure of LTP induction. (C) 2015 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:我们研究了在预处理低频刺激(LFS)期间激活的肌醇1,4,5-三磷酸受体(IP(3)Rs)在随后的高频刺激(HFS)诱导的长期增强诱导中的作用( LTP)在成熟豚鼠海马切片的CA1神经元中。通过将HFS(100 Hz时的100个脉冲的破伤风)递送至向CA1神经突触的Schaffer侧支连合途径传递LFS,可在野外兴奋性突触后电位(EPSP)或种群突增(PS)中诱导LTP。通过1000 Hz的LFS在1 Hz下进行预处理。当在N-甲基-D-天门冬氨酸受体(NMDARs)拮抗剂,代谢型谷氨酸受体(mGluR)拮抗剂,IP3R拮抗剂,钙调蛋白依赖性激酶II抑制剂或钙调神经磷酸酶存在下应用预处理LFS时,该作用被抑制。抑制剂。此外,在递送HFS之前立即阻断I组mGluRs可以阻止预处理LFS对随后的HFS诱导LTP的抑制作用。这些结果表明,在海马CA1神经突触中,在预处理LFS期间NMDARs和IP(3)Rs的共激活会导致磷酸化和去磷酸化事件,从而导致导致LTP失败的I类mGluRs的激活时间延长。感应。 (C)2015年IBRO。由Elsevier Ltd.出版。保留所有权利。

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