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本文引用的文献

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17beta-Estradiol Induction of Filopodial Growth in Cultured Hippocampal Neurons within Minutes of Exposure.17β-雌二醇在暴露于培养的海马神经元数分钟内诱导丝状伪足生长。
Mol Cell Neurosci. 1993 Feb;4(1):36-46. doi: 10.1006/mcne.1993.1005.
2
Estrogen receptor alpha and beta specific agonists regulate expression of synaptic proteins in rat hippocampus.雌激素受体α和β特异性激动剂调节大鼠海马体中突触蛋白的表达。
Brain Res. 2009 Sep 22;1290:1-11. doi: 10.1016/j.brainres.2009.06.090. Epub 2009 Jul 9.
3
Gonadal hormones modulate the dendritic spine densities of primary cortical pyramidal neurons in adult female rat.性腺激素调节成年雌性大鼠大脑皮质锥体神经元树突棘密度。
Cereb Cortex. 2009 Nov;19(11):2719-27. doi: 10.1093/cercor/bhp048. Epub 2009 Mar 17.
4
Assessment of estradiol influence on spatial tasks and hippocampal CA1 spines: evidence that the duration of hormone deprivation after ovariectomy compromises 17beta-estradiol effectiveness in altering CA1 spines.雌二醇对空间任务及海马CA1区脊柱的影响评估:证据表明卵巢切除术后激素剥夺的持续时间会损害17β -雌二醇改变CA1区脊柱的有效性。
Horm Behav. 2008 Aug;54(3):386-95. doi: 10.1016/j.yhbeh.2008.04.010. Epub 2008 May 9.
5
17beta-estradiol modifies stress-induced and age-related changes in hippocampal synaptic plasticity.17β-雌二醇可改变应激诱导的及与年龄相关的海马突触可塑性变化。
Behav Neurosci. 2008 Apr;122(2):301-9. doi: 10.1037/0735-7044.122.2.301.
6
Two-photon imaging of dendritic spine development in the mouse cortex.小鼠皮层树突棘发育的双光子成像
Dev Neurobiol. 2008 May;68(6):771-8. doi: 10.1002/dneu.20630.
7
Estrogen and aging affect synaptic distribution of phosphorylated LIM kinase (pLIMK) in CA1 region of female rat hippocampus.雌激素和衰老影响雌性大鼠海马体CA1区磷酸化LIM激酶(pLIMK)的突触分布。
Neuroscience. 2008 Mar 18;152(2):360-70. doi: 10.1016/j.neuroscience.2008.01.004. Epub 2008 Jan 12.
8
Uncovering the mechanisms of estrogen effects on hippocampal function.揭示雌激素对海马体功能影响的机制。
Front Neuroendocrinol. 2008 May;29(2):219-37. doi: 10.1016/j.yfrne.2007.08.006. Epub 2007 Oct 15.
9
Brain aging modulates the neuroprotective effects of estrogen on selective aspects of cognition in women: a critical review.脑老化调节雌激素对女性认知特定方面的神经保护作用:一项批判性综述。
Front Neuroendocrinol. 2008 Jan;29(1):88-113. doi: 10.1016/j.yfrne.2007.08.002. Epub 2007 Oct 1.
10
Interactive effects of age and estrogen on cognition and pyramidal neurons in monkey prefrontal cortex.年龄与雌激素对猴前额叶皮质认知及锥体神经元的交互作用。
Proc Natl Acad Sci U S A. 2007 Jul 3;104(27):11465-70. doi: 10.1073/pnas.0704757104. Epub 2007 Jun 25.

雌激素与衰老大脑:疲惫皮质网络的灵丹妙药。

Estrogen and the aging brain: an elixir for the weary cortical network.

机构信息

Department of Neuroscience, Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, New York, USA.

出版信息

Ann N Y Acad Sci. 2010 Aug;1204:104-12. doi: 10.1111/j.1749-6632.2010.05529.x.

DOI:10.1111/j.1749-6632.2010.05529.x
PMID:20738280
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2951002/
Abstract

The surprising discovery in 1990 that estrogen modulates hippocampal structural plasticity launched a whole new field of scientific inquiry. Over the past two decades, estrogen-induced spinogenesis has been described in several brain areas involved in cognition in a number of species, in both sexes and on multiple time scales. Exploration into the interaction between estrogen and aging has illuminated some of the hormone's neuroprotective effects, most notably on age-related cognitive decline in nonhuman primates. Although there is still much to be learned about the mechanisms by which estrogen exerts its actions, key components of the signal transduction pathways are beginning to be elucidated and nongenomic actions via membrane bound estrogen receptors are of particular interest. Future studies are focused on identifying the most clinically relevant hormone treatment, as well as the potential identification of new therapeutics that can prevent or reverse age-related cognitive impairment by intercepting specific signal transduction pathways initiated by estrogen.

摘要

1990 年令人惊讶的发现,雌激素调节海马体结构可塑性,开启了全新的科学研究领域。在过去的二十年中,雌激素诱导的树突棘形成已在多个物种的几个认知相关脑区中被描述,涉及两性和多个时间尺度。对雌激素与衰老相互作用的探索阐明了激素的一些神经保护作用,尤其是在非人类灵长类动物与年龄相关的认知衰退方面。尽管关于雌激素发挥作用的机制还有很多需要了解,但信号转导途径的关键组成部分开始被阐明,通过膜结合雌激素受体的非基因组作用尤其受到关注。未来的研究集中在确定最具临床相关性的激素治疗方法,以及通过阻断雌激素引发的特定信号转导途径,鉴定潜在的新疗法,以预防或逆转与年龄相关的认知障碍。