首页> 外文期刊>The Journal of Physiology >Synaptically activated Ca2+ waves in layer 2/3 and layer 5 rat neocortical pyramidal neurons.
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Synaptically activated Ca2+ waves in layer 2/3 and layer 5 rat neocortical pyramidal neurons.

机译:在第2/3和第5层大鼠新皮层锥体神经元中被突触激活的Ca2 +波。

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Calcium waves in layer 2/3 and layer 5 neocortical somatosensory pyramidal neurons were examined in slices from 2- to 8-week-old rats. Repetitive synaptic stimulation evoked a delayed, all-or-none [Ca2+]i increase primarily on the main dendritic shaft. This component was blocked by 1 mM (R,S)-alpha-methyl-4-carboxyphenylglycine (MCPG), 10 microM ryanodine, 1 mg ml-1 internal heparin, and was not blocked by 400 microM internal Ruthenium Red, indicating that it was due to Ca2+ release from internal stores by inositol 1,4,5-trisphosphate (IP3) mobilized via activation of metabotropic glutamate receptors. Calcium waves were initiated on the apical shaft at sites between the soma to around the main branch point, mostly at insertion points of oblique dendrites, and spread in both directions along the shaft. In the proximal dendrites the peak amplitude of the resulting [Ca2+]i change was much larger than that evoked by a train of Na+ spikes. In distal dendrites the peak amplitude was comparable to the [Ca2+]ichange due to a Ca2+ spike. IP3-mediated Ca2+ release also was observed in the presence of the metabotropic agonists t-ACPD and carbachol when backpropagating spikes were generated. Ca2+ entry through NMDA receptors was observed primarily on the oblique dendrites. The main differences between waves in neocortical neurons and in previously described hippocampal pyramidal neurons were, (a) Ca2+ waves in L5 neurons could be evoked further out along the main shaft, (b) Ca2+ waves extended slightly further out into the oblique dendrites and (c) higher concentrations of bath-applied t-ACPD and carbachol were required to generate Ca2+ release events by backpropagating action potentials.
机译:在2至8周龄大鼠的切片中检查了第2/3层和第5层新皮层体感锥体神经元中的钙波。重复的突触刺激引起主要的树突状干延迟或全部[Ca2 +] i增加。该成分被1 mM(R,S)-α-甲基-4-羧基苯基甘氨酸(MCPG),10 microM ryanodine,1 mg ml-1内部肝素阻断,未被400 microM内部钌红阻断,表明这是由于通过代谢型谷氨酸受体活化而动员的肌醇1,4,5-三磷酸(IP3)从内部存储中释放的Ca2 +。钙波在躯干到主要分支点之间的位置处(主要在倾斜的树突的插入点处)在顶轴上引发,并沿轴在两个方向上传播。在近端树突中,所产生的[Ca2 +] i变化的峰值幅度比一系列Na +尖峰引起的峰值幅度大得多。在远端树突中,由于Ca2 +尖峰,峰值幅度可与[Ca2 +] ichange相媲美。当产生向后传播的尖峰时,在存在促代谢激动剂t-ACPD和卡巴胆碱的情况下,也观察到IP3介导的Ca2 +释放。 Ca2 +通过NMDA受体进入主要在倾斜的树突上观察到。在新皮层神经元和先前描述的海马锥体神经元中,波的主要区别在于:(a)L5神经元中的Ca2 +波可沿主轴进一步诱发,(b)Ca2 +波稍稍向斜枝突延伸,并且( c)通过反向传播动作电位,需要更高浓度的浸浴t-ACPD和卡巴胆碱来产生Ca2 +释放事件。

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