首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >N-methyl-d-aspartate receptor-dependent long-term potentiation in CA1 region affects synaptic expression of glutamate receptor subunits and associated proteins in the whole hippocampus.
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N-methyl-d-aspartate receptor-dependent long-term potentiation in CA1 region affects synaptic expression of glutamate receptor subunits and associated proteins in the whole hippocampus.

机译:CA1区的N-甲基-d-天冬氨酸受体依赖性长期增强作用会影响整个海马中谷氨酸受体亚基和相关蛋白的突触表达。

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摘要

Long term potentiation in hippocampus, evoked by high-frequency stimulation, is mediated by two major glutamate receptor subtypes, alpha-amino-3-hydroxyl-5-methyl-4-isoxazole propionate receptors and N-methyl-d-aspartate receptors. Receptor subunit composition and its interaction with cytoplasmic proteins constitute different pathways regulating synaptic plasticity. Here, we provide further evidence that N-methyl-d-aspartate receptor-mediated long term potentiation evoked at hippocampal CA1 region of rats induced by high-frequency stimulation of the Schaffer collateral-commissural pathway in vivo is not dependent on N-methyl-d-aspartate receptor subunit NR2B. Applying semi-quantitative immunoblotting, we found that in the whole tetanized hippocampus, synaptic expression of the N-methyl-d-aspartate and alpha-amino-3-hydroxyl-5-methyl-4-isoxazole propionate receptor subunits (NR1, NR2A, glutamate receptor 1) and their associated partners, e.g. synaptic associated protein 97, postsynaptic density protein 95, alpha subunit of Ca(2+)/calmodulin-dependent protein kinase II, neuronal nitricoxide synthase, increased 180 min post-high-frequency stimulation. Moreover, phosphorylation of Ca(2+)/calmodulin-dependent protein kinase II at thr286 and glutamate receptor 1 at ser831 was increased 30 min post-high-frequency stimulation and blocked by N-methyl-d-aspartate receptor antagonists (AP-5 and MK-801). In sham group and controls, these changes were not observed. The expression of several other synaptic proteins (NR2B, glutamate receptors 2/3, N-ethylmaleimide sensitive factor) was not affected by long term potentiation induction. In hippocampal homogenates, the level of these proteins remained unchanged. These data indicate that N-methyl-d-aspartate receptor-dependent long term potentiation in CA1 region in vivo mainly affects the synaptic expression of glutamate receptor subunits and associated proteins in the whole hippocampus. The alteration of molecular aspects can play a role in regulating the long-lasting synaptic modification in hippocampal long term potentiation in vivo.
机译:高频刺激引起的海马长时程增强是由两种主要的谷氨酸受体亚型介导的,分别是丙酸α-氨基-3-羟基-5-甲基-4-异恶唑丙酸酯受体和N-甲基-d-天冬氨酸受体。受体亚基组成及其与细胞质蛋白的相互作用构成了调节突触可塑性的不同途径。在这里,我们提供了进一步的证据,表明高频体内刺激Schaffer侧连合途径的大鼠在海马CA1区诱发了N-甲基-d-天冬氨酸受体介导的长期增强作用,该作用不依赖于N-甲基- d-天冬氨酸受体亚基NR2B。应用半定量免疫印迹法,我们发现在整个成群的海马中,N-甲基-d-天门冬氨酸和α-氨基-3-羟基-5-甲基-4-异恶唑丙酸酯受体亚基(NR1,NR2A,谷氨酸受体1)及其相关伴侣,例如突触相关蛋白97,突触后密度蛋白95,Ca(2 +)/钙调蛋白依赖性蛋白激酶II,神经元一氧化氮合酶的α亚基,在高频刺激后增加180分钟。此外,高频刺激后30分钟,在thr286处Ca(2 +)/钙调蛋白依赖性蛋白激酶II和ser831处的谷氨酸受体1的磷酸化增加,并被N-甲基-d-天冬氨酸受体拮抗剂(AP-5和MK-801)。在假手术组和对照组中,未观察到这些变化。长期增强诱导不影响其他几种突触蛋白(NR2B,谷氨酸受体2/3,N-乙基马来酰亚胺敏感因子)的表达。在海马匀浆中,这些蛋白质的水平保持不变。这些数据表明体内CA1区域中的N-甲基-d-天冬氨酸受体依赖性长期增强主要影响整个海马中谷氨酸受体亚基和相关蛋白的突触表达。分子方面的改变可以在体内调节海马长期增强中的长效突触修饰中发挥作用。

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