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Kainate receptors in hippocampal CA3 subregion: evidence for a role in regulating neurotransmitter release.

机译:海马CA3区域的海藻酸酯受体:在调节神经递质释放中起作用的证据。

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The hippocampal CA3 subregion of the rat is characteristically enriched in kainate receptors. At the synaptic level, the subcellular localization of these receptors is still a matter of debate. The CA3 pyramidal cells are particularly sensitive to excitotoxicity induced by kainate, which is in agreement with the high levels of kainate receptors in the stratum lucidum of the hippocampal CA3 subregion. Immunocytochemical studies, using antibodies against kainate receptor subunits, clearly demonstrated the presence of postsynaptic kainate receptors. However, it was not possible at the time to identify the activity of postsynaptic kainate receptors as mediators of the synaptic transmission. There are also reports showing the labeling of unmyelinated axons and nerve terminals with antibodies against kainate receptor subunits. The evidence for the presence of presynaptic kainate receptors in the hippocampus is further substantiated by the demonstration that stimulation of kainate receptors in synaptosomes isolated from the rat hippocampal CA3 subregion increases the intracellular free Ca2+ concentration ([Ca2+]i) coupled to the release of glutamate. These results support the model proposed by Coyle (1983), in which the excitotoxicity induced by kainate involves the activation of presynaptic kainate receptors, causing the release of glutamate. According to this model, the neurotoxic effect of kainate in the rat hippocampal CA3 subregion involves a direct effect on presynaptic kainate receptors and an indirect effect on postsynaptic glutamate receptors due to the enhanced release of glutamate.
机译:大鼠的海马CA3子区域特征性地富含海藻酸盐受体。在突触水平,这些受体的亚细胞定位仍然是一个争论的问题。 CA3锥体细胞对海藻酸盐诱导的兴奋性毒性特别敏感,这与海马CA3亚区的透明层中的高水平的海藻酸盐受体一致。使用抗海藻酸盐受体亚基的抗体进行的免疫细胞化学研究清楚地表明了突触后海藻酸盐受体的存在。然而,当时尚无法确定突触后海藻酸盐受体作为突触传递介质的活性。也有报道显示未磷酸化的轴突和神经末梢用抗海藻酸盐受体亚基的抗体标记。海马中存在突触前海藻酸受体的证据进一步得到了证实,即从大鼠海马CA3子区域分离的突触体中刺激海藻酸受体会增加细胞内游离Ca2 +浓度([Ca2 +] i)并与谷氨酸的释放相关。这些结果支持了Coyle(1983)提出的模型,其中由海藻酸盐引起的兴奋性毒性涉及突触前海藻酸盐受体的激活,从而导致谷氨酸的释放。根据该模型,海藻酸盐在大鼠海马CA3子区域的神经毒性作用包括对突触前海藻酸盐受体的直接作用,以及由于谷氨酸释放量增加对突触后谷氨酸盐受体的间接作用。

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