4.7 Article

Hippocampal Granule Neuron Number and Dentate Gyrus Volume in Antidepressant-Treated and Untreated Major Depression

期刊

NEUROPSYCHOPHARMACOLOGY
卷 38, 期 6, 页码 1068-1077

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/npp.2013.5

关键词

NeuN; postmortem; stereology; plasticity; psychopharmacology; serotonin

资金

  1. American Foundation for Suicide Prevention
  2. Diane Goldberg Foundation
  3. GlaxoSmithKline
  4. Novartis
  5. [MH83862]
  6. [MH94888]
  7. [MH64168]

向作者/读者索取更多资源

Smaller hippocampal volume is reported in major depressive disorder (MDD). We hypothesize that it may be related to fewer granule neurons (GN) in the dentate gyrus (DG), a defect possibly reversible with antidepressants. We studied age-, sex-, and postmortem interval-matched groups: no major psychopathology (controls); unmedicated-MDD; and MDD treated with serotonin reuptake inhibitors (MDD*SSRI) or tricyclics (MDD*TCA). Frozen right hippocampi were fixed, sectioned (50 mu m), immunostained with neuronal nuclear marker (NeuN), and counterstained with hematoxylin. GN and glial number, and DG and granule cell layer (GCL) volumes were stereologically estimated. Fewer GNs in the anterior DG were present in unmedicated-MDDs compared with controls (p = 0.013). Younger age of MDD onset correlated with fewer GNs (p = 0.021). Unmedicated-MDDs had fewer mid-DG GNs than MDD*SSRIs (p = 0.028) and controls (p = 0.032). Anterior GCL glial number did not differ between groups. Anterior/mid GCL volume was smaller in unmedicated-MDDs vs controls (p = 0.008) and larger in MDD*SSRIs vs unmedicated-MDDs (p<0.001), MDD*TCAs (p<0.001), and controls (p<0.001). Anterior GCL volume and GN number (r = 0.594, p = 0.001), and mid DG volume and GN number (r = 0.398, p = 0.044) were correlated. Anterior DG capillary density correlated with GN number (p = 0.027), and with GCL (p = 0.024) and DG (r = 0.400, p = 0.047) volumes. Posterior DG volume and GN number did not differ between groups. Fewer GNs in unmedicated-MDD without fewer neuronal progenitor cells, as previously reported, suggests a cell maturation or survival defect, perhaps related to MDD duration. This may contribute to a smaller hippocampus and is potentially reversed by SSRIs. Postmortem studies are correlative and animal studies are needed to test implied causal relationships. Neuropsychopharmacology (2013) 38, 1068-1077; doi:10.1038/npp.2013.5; published online 23 January 2013

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据