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雌二醇可诱导成年雌性大鼠海马CA1区和CA3区出现阶段性的Fos反应。

Estradiol induces a phasic Fos response in the hippocampal CA1 and CA3 regions of adult female rats.

作者信息

Rudick C N, Woolley C S

机构信息

Department of Neurobiology and Physiology, Northwestern University, Evanston, Illinois 60208, USA.

出版信息

Hippocampus. 2000;10(3):274-83. doi: 10.1002/1098-1063(2000)10:3<274::AID-HIPO8>3.0.CO;2-Q.

Abstract

Previous studies have shown that estradiol induces structural and functional changes in hippocampal CA1 pyramidal cells of the adult female rat. Estradiol increases the density of dendritic spines and axospinous synapses on CA1 pyramidal cells, and increases these cells' sensitivity to NMDA receptor-mediated synaptic input. Curiously, while estradiol effects are observed in CA1 pyramidal cells, the majority of the evidence indicates that these cells lack genomic estradiol receptors. In contrast, genomic estradiol receptors are expressed in at least some hippocampal interneurons in CA1. The goal of the present study was to determine which hippocampal neuronal populations are activated by estradiol, as determined by induction of c-Fos immunoreactivity, as well as the time-course of this activation. We quantified c-Fos expression in each of the major subdivisions of the hippocampus in adult female rats at various time points during the same estradiol treatment regimen known to regulate dendritic spines and synapses on CA1 pyramidal cells. Our results show a phasic estradiol-induced c-Fos response in the pyramidal cell layers of both CA1 and CA3. c-Fos was induced within 2 h of treatment, decreased at 6 and 12 h, and subsequently increased again at 24 h after treatment with estradiol. Double labeling for c-Fos and GAD 65 or GAD 67 suggests that c-Fos is induced primarily in principal cells, though a small proportion of GABAergic cells is also labeled. These estradiol-induced changes in c-Fos expression may reflect phasic neuronal activation and coupling to gene expression, which could be involved in estradiol's effects on excitatory synaptic connectivity in the hippocampus.

摘要

先前的研究表明,雌二醇会诱导成年雌性大鼠海马CA1锥体细胞发生结构和功能变化。雌二醇会增加CA1锥体细胞上树突棘和轴棘突触的密度,并提高这些细胞对NMDA受体介导的突触输入的敏感性。奇怪的是,虽然在CA1锥体细胞中观察到了雌二醇的作用,但大多数证据表明这些细胞缺乏基因组雌二醇受体。相比之下,基因组雌二醇受体至少在CA1区的一些海马中间神经元中表达。本研究的目的是确定哪些海马神经元群体被雌二醇激活,这通过诱导c-Fos免疫反应性来确定,以及这种激活的时间进程。我们在已知可调节CA1锥体细胞上树突棘和突触的相同雌二醇治疗方案的不同时间点,对成年雌性大鼠海马各主要亚区的c-Fos表达进行了量化。我们的结果显示,在CA1和CA3的锥体细胞层中,雌二醇诱导了阶段性的c-Fos反应。在雌二醇处理后2小时内诱导出c-Fos,在6小时和12小时时下降,随后在24小时时再次升高。对c-Fos和GAD 65或GAD 67进行双重标记表明,c-Fos主要在主细胞中被诱导,尽管也有一小部分GABA能细胞被标记。这些雌二醇诱导的c-Fos表达变化可能反映了阶段性的神经元激活以及与基因表达的耦合,这可能与雌二醇对海马兴奋性突触连接的影响有关。

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