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Apoptosis in schizophrenia: pathophysiologic and therapeutic considerations.
Curr Opin Psychiatry. 2006 May;19(3):307-12. doi: 10.1097/01.yco.0000218603.25346.8f.
2
A schizophrenia-associated mutation of DISC1 perturbs cerebral cortex development.DISC1基因的一种与精神分裂症相关的突变扰乱了大脑皮层发育。
Nat Cell Biol. 2005 Dec;7(12):1167-78. doi: 10.1038/ncb1328. Epub 2005 Nov 20.
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Genetics. Two genes link two distinct psychoses.遗传学。两个基因将两种不同的精神病联系起来。
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DISC1 and neurocognitive function in schizophrenia.
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Association between genotype at an exonic SNP in DISC1 and normal cognitive aging.
Neurosci Lett. 2005 Nov 25;389(1):41-5. doi: 10.1016/j.neulet.2005.07.004.
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Reelin glycoprotein: structure, biology and roles in health and disease.Reelin糖蛋白:结构、生物学特性及其在健康与疾病中的作用
Mol Psychiatry. 2005 Mar;10(3):251-7. doi: 10.1038/sj.mp.4001613.
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Levels of Bcl-2 and P53 are altered in superior frontal and cerebellar cortices of autistic subjects.自闭症患者额上回和小脑皮质中Bcl-2和P53的水平发生改变。
Cell Mol Neurobiol. 2003 Dec;23(6):945-52. doi: 10.1023/b:cemn.0000005322.27203.73.
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Apoptotic proteins in the temporal cortex in schizophrenia: high Bax/Bcl-2 ratio without caspase-3 activation.精神分裂症患者颞叶皮质中的凋亡蛋白:Bax/Bcl-2比值升高但无半胱天冬酶-3激活。
Am J Psychiatry. 2004 Jan;161(1):109-15. doi: 10.1176/appi.ajp.161.1.109.
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Two-dimensional assessment of cytoarchitecture in the anterior cingulate cortex in major depressive disorder, bipolar disorder, and schizophrenia: evidence for decreased neuronal somal size and increased neuronal density.重度抑郁症、双相情感障碍和精神分裂症患者前扣带回皮质细胞结构的二维评估:神经元胞体大小减小和神经元密度增加的证据
Biol Psychiatry. 2003 Jun 15;53(12):1086-98. doi: 10.1016/s0006-3223(03)00114-8.
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Purkinje cell size is reduced in cerebellum of patients with autism.自闭症患者小脑的浦肯野细胞大小减小。
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双相情感障碍患者海马CA1区锥体细胞体积减小。

Hippocampal CA1 pyramidal cell size is reduced in bipolar disorder.

作者信息

Liu Lusha, Schulz S Charles, Lee Susanne, Reutiman Teri J, Fatemi S Hossein

机构信息

Department of Psychiatry, University of Minnesota, 420 Delaware Street SE, Minneapolis, MN 55455, USA.

出版信息

Cell Mol Neurobiol. 2007 May;27(3):351-8. doi: 10.1007/s10571-006-9128-7. Epub 2007 Jan 19.

DOI:10.1007/s10571-006-9128-7
PMID:17235693
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11517201/
Abstract
  1. Schizophrenia and bipolar disorder are neurodevelopmental disorders with significant genetic vulnerabilities. Several trophic genes and/or proteins have been implicated in the causation for both disorders.2. We hypothesized that these genes and/or proteins may impact neuronal growth in both disorders.3. Hippocampal tissue sections from CA1 area of schizophrenic, bipolar, depressed, and controls subjects, matched for age, sex, PMI, drug exposure, and brain pH were prepared for cell size determination using the Stanley Medical Research Foundation postmortem brain collection.4. Quantification of hippocampal CA1 pyramidal neuron size showed a significant 12% reduction in cell size (p < 0.05) in bipolar subjects vs. controls. There were nonsignificant trends for reduction in cell size in both schizophrenic and depressed subjects vs. controls.5. These results indicate for the first time that pyramidal cell atrophy is present in hippocampus of subjects with bipolar disorder.
摘要
  1. 精神分裂症和双相情感障碍是具有显著遗传易感性的神经发育障碍。几种营养基因和/或蛋白质与这两种疾病的病因有关。

  2. 我们假设这些基因和/或蛋白质可能会影响这两种疾病中的神经元生长。

  3. 使用斯坦利医学研究基金会的尸检脑库,制备了来自精神分裂症、双相情感障碍、抑郁症患者以及年龄、性别、PMI、药物暴露和脑pH值相匹配的对照组受试者CA1区的海马组织切片,用于测定细胞大小。

  4. 海马CA1区锥体神经元大小的量化显示,与对照组相比,双相情感障碍患者的细胞大小显著减少了12%(p < 0.05)。精神分裂症患者和抑郁症患者与对照组相比,细胞大小减少的趋势不显著。

  5. 这些结果首次表明,双相情感障碍患者的海马中存在锥体细胞萎缩。