Woolley C S, Weiland N G, McEwen B S, Schwartzkroin P A
Department of Neurological Surgery, University of Washington, Seattle, Washington 98195, USA.
J Neurosci. 1997 Mar 1;17(5):1848-59. doi: 10.1523/JNEUROSCI.17-05-01848.1997.
Previous studies have shown that estradiol induces new dendritic spines and synapses on hippocampal CA1 pyramidal cells. We have assessed the consequences of estradiol-induced dendritic spines on CA1 pyramidal cell intrinsic and synaptic electrophysiological properties. Hippocampal slices were prepared from ovariectomized rats treated with either estradiol or oil vehicle. CA1 pyramidal cells were recorded and injected with biocytin to visualize spines. The association of dendritic spine density and electrophysiological parameters for each cell was then tested using linear regression analysis. We found a negative relationship between spine density and input resistance; however, no other intrinsic property measured was significantly associated with dendritic spine density. Glutamate receptor autoradiography demonstrated an estradiol-induced increase in binding to NMDA, but not AMPA, receptors. We then used input/output (I/O) curves (EPSP slope vs stimulus intensity) to determine whether the sensitivity of CA1 pyramidal cells to synaptic input is correlated with dendritic spine density. Consistent with the lack of an estradiol effect on AMPA receptor binding, we observed no relationship between the slope of an I/O curve generated under standard recording conditions, in which the AMPA receptor dominates the EPSP, and spine density. However, recording the pharmacologically isolated NMDA receptor-mediated component of the EPSP revealed a significant correlation between I/O slope and spine density. These results indicate that, in parallel with estradiol-induced increases in spine/synapse density and NMDA receptor binding, estradiol treatment increases sensitivity of CA1 pyramidal cells to NMDA receptor-mediated synaptic input; further, sensitivity to NMDA receptor-mediated synaptic input is well correlated with dendritic spine density.
先前的研究表明,雌二醇可诱导海马CA1锥体神经元产生新的树突棘和突触。我们评估了雌二醇诱导的树突棘对CA1锥体神经元内在和突触电生理特性的影响。从接受雌二醇或油剂处理的去卵巢大鼠制备海马脑片。记录CA1锥体神经元,并注射生物胞素以观察树突棘。然后使用线性回归分析测试每个细胞的树突棘密度与电生理参数之间的相关性。我们发现树突棘密度与输入电阻之间呈负相关;然而,所测量的其他内在特性与树突棘密度均无显著相关性。谷氨酸受体放射自显影显示,雌二醇诱导与NMDA受体而非AMPA受体的结合增加。然后我们使用输入/输出(I/O)曲线(兴奋性突触后电位斜率与刺激强度)来确定CA1锥体神经元对突触输入的敏感性是否与树突棘密度相关。与雌二醇对AMPA受体结合缺乏影响一致,我们观察到在标准记录条件下(其中AMPA受体主导兴奋性突触后电位)生成的I/O曲线斜率与树突棘密度之间没有关系。然而,记录药理学分离的NMDA受体介导的兴奋性突触后电位成分显示,I/O斜率与树突棘密度之间存在显著相关性。这些结果表明,与雌二醇诱导的树突棘/突触密度增加和NMDA受体结合增加并行,雌二醇处理增加了CA1锥体神经元对NMDA受体介导的突触输入的敏感性;此外,对NMDA受体介导的突触输入的敏感性与树突棘密度密切相关。