...
首页> 外文期刊>Journal of neurobiology >Dendritic morphology is altered in hippocampal neurons following prenatal compromise.
【24h】

Dendritic morphology is altered in hippocampal neurons following prenatal compromise.

机译:产前受损后海马神经元的树突形态发生改变。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Chronic placental insufficiency (CPI), a known cause of intrauterine growth restriction, can lead to structural alterations in the developing brain that might underlie postnatal neurological deficits. We have previously demonstrated significant reductions in the volumes of hippocampal neuropil layers in fetal guinea pig brains following experimentally induced growth restriction. To determine the components of the neuropil affected in the brains of growth restricted (GR) fetuses, the dendritic morphology of CA1 pyramidal neurons and dentate granule cells was examined. CPI was induced by unilateral uterine artery ligation in pregnant guinea pigs at midgestation (term approximately 67days). Hippocampi from control and GR fetuses were stained using the Rapid Golgi technique and the growth and branching of the dendritic arbors were quantified using the Sholl method. In addition, the density of dendritic spines was determined on the apical arbors of each population. In GR brains (n = 7) compared to controls (n = 7), there was a reduction in dendritic elongation (p < 0.005) and an alteration in the branch point distribution in CA1 basal arbors, and a reduction both in the outgrowth (p < 0.05) and branch point number (p < 0.05) of CA1 apical arbors. Dentate granule cells from GR brains also demonstrated reduced dendritic outgrowth (p < 0.05). There was an increase in dendritic spine density in both neuronal populations; this might be due either to altered synaptic pruning or as a compensatory mechanism for reduced dendritic length. These findings demonstrate that a chronic prenatal insult causes selective changes in the morphology of hippocampal cell dendrites and may lead to alterations in hippocampal function in the postnatal period. Copyright 2003 Wiley Periodicals, Inc. J Neurobiol 55: 41-52, 2003
机译:慢性胎盘功能不全(CPI)是子宫内生长受限的已知原因,可导致发育中的大脑结构改变,可能是产后神经功能缺损的基础。我们先前已经证明,实验诱导的生长受限后,胎儿豚鼠脑中海马神经丛层的体积显着减少。为了确定生长受限(GR)胎儿的大脑中受影响的神经药的成分,检查了CA1锥体神经元和齿状颗粒细胞的树突形态。在妊娠中期(每学期约67天),对怀孕的豚鼠进行单侧子宫动脉结扎诱导CPI。使用快速高尔基体技术对来自对照和GR胎儿的海马进行染色,并使用Sholl方法对树突状树突的生长和分支进行定量。此外,树突棘的密度是在每个种群的根茎上确定的。与对照组(n = 7)相比,GR大脑(n = 7)的树突伸长率降低(p <0.005),CA1基底乔木中的分支点分布发生变化,并且向外生长均降低( p <0.05)和CA1根茎的分支点数(p <0.05)。来自GR脑的齿状颗粒细胞也显示出减少的树突生长(p <0.05)。在两个神经元人群中,树突棘密度均增加。这可能是由于突触修剪的改变或由于树突长度减少的补偿机制所致。这些发现表明,产前慢性损伤会导致海马细胞树突形态发生选择性变化,并可能导致产后海马功能发生变化。版权所有2003 Wiley Periodicals,Inc. J Neurobiol 55:41-52,2003

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号