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代谢型谷氨酸受体激活可诱导海马树突内的钙波。

Metabotropic glutamate receptor activation induces calcium waves within hippocampal dendrites.

作者信息

Jaffe D B, Brown T H

机构信息

Department of Psychology, Yale University, New Haven, Connecticut 06520-8205.

出版信息

J Neurophysiol. 1994 Jul;72(1):471-4. doi: 10.1152/jn.1994.72.1.471.

Abstract
  1. We investigated the effects of metabotropic glutamate (mGlu) receptor activation on intracellular Ca2+ concentration ([Ca2+]i) in the soma and dendrites of hippocampal CA1 pyramidal neurons. Changes in [Ca2+]i were measured using confocal imaging simultaneously with whole-cell recording techniques. Differences in [Ca2+]i were visualized as changes in the fluorescence of the Ca(2+)-sensitive dye Fluo-3. 2. Brief application of the specific mGlu receptor agonist (1S,3R)-ACPD to either the apical or basal dendrites produced initially localized increases in [Ca2+]i that subsequently propagated as waves throughout much of the neuron. These Ca2+ waves, which propagated at approximately 40 microns/s, were shown not to reflect intracellular Ca2+ diffusion or extracellular diffusion of ACPD and were always accompanied by small outward membrane currents. 3. Repetitive application of ACPD failed to trigger further Ca2+ release. We found that a threshold level of voltage-gated Ca2+ entry during trains of action potentials was needed to prime further mGlu-stimulated Ca2+ release. In contrast, the passage of time alone did not cause the mGlu-release system to reactivate--restoration of ACPD-stimulated Ca2+ release. The spike-mediated Ca2+ signal was unaffected by mGlu-stimulated depletion of intracellular stores. 4. These experiments demonstrate that specific mGlu receptor activation can mobilize Ca2+ in dendrites of CA1 neurons and trigger waves of Ca(2+)-induced Ca(2+)-release throughout the cell. A use-dependent relationship between voltage-gated Ca2+ entry during trains of action potentials and mGlu-stimulated Ca2+ release is suggested.
摘要
  1. 我们研究了代谢型谷氨酸(mGlu)受体激活对海马CA1锥体神经元胞体和树突内细胞内钙离子浓度([Ca2+]i)的影响。使用共聚焦成像结合全细胞记录技术测量[Ca2+]i的变化。[Ca2+]i的差异通过钙敏感染料Fluo-3荧光的变化来可视化。2. 向顶端或基部树突短暂施加特异性mGlu受体激动剂(1S,3R)-ACPD,最初会使[Ca2+]i在局部增加,随后以波的形式传播至神经元的大部分区域。这些以约40微米/秒的速度传播的Ca2+波,被证明并非反映细胞内Ca2+扩散或ACPD的细胞外扩散,并且总是伴随着小的外向膜电流。3. 重复施加ACPD未能触发进一步的Ca2+释放。我们发现,在动作电位串期间,电压门控Ca2+进入需要达到阈值水平才能引发进一步的mGlu刺激的Ca2+释放。相比之下,仅时间的推移并不会导致mGlu释放系统重新激活——恢复ACPD刺激的Ca2+释放。动作电位介导的Ca2+信号不受mGlu刺激引起的细胞内储存耗尽的影响。4. 这些实验表明,特异性mGlu受体激活可动员CA1神经元树突中的Ca2+,并触发整个细胞内Ca2+诱导的Ca2+释放波。提示了动作电位串期间电压门控Ca2+进入与mGlu刺激的Ca2+释放之间的使用依赖关系。

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