Low glial numbers in the amygdala in major depressive disorder

被引:380
作者
Bowley, MP
Drevets, WC
Öngür, D
Price, JL
机构
[1] Washington Univ, Sch Med, Dept Anat & Neurobiol, St Louis, MO 63110 USA
[2] NIMH, Mood & Anxiety Disorders Program, Bethesda, MD 20892 USA
关键词
major depressive disorder; bipolar disorder; amygdala; entorhinal cortex; glia; lithium; valproate;
D O I
10.1016/S0006-3223(02)01404-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Functional imaging studies implicate the prefrontal cortex and amygdala in major depressive disorder and bipolar disorder, and glial decreases have been reported in the prefrontal cortex. Here, glia and neurons were counted in the amygdala and entorhinal cortex in major depressive disorder, bipolar disorder, and control cases. Methods: Tissue blocks from major depressive disorder (7), bipolar disorder (10), and control (12) cases, equally divided between right and left, were cut into 50 mum sections and stained with the Nissl method. One major depressive disorder and all but two bipolar disorder cases had been treated with lithium or valproate. Neurons and glia were counted using stereological methods. Results: Glial density and the glia/neuron ratio were substantially reduced in the amygdala in major depressive disorder cases. The reduction was mainly accounted for by counts in the left hemisphere. No change was found in neurons. Average glia measures were not reduced in bipolar disorder cases; however, bipolar disorder cases not treated with lithium or valproate had significant glial reduction. Similar but smaller changes were found in the entorhinal cortex. Conclusions: Glia are reduced in the amygdala in major depressive disorder, especially on the left side. The results suggest that lithium and valproate may moderate the glial reduction.
引用
收藏
页码:404 / 412
页数:9
相关论文
共 66 条
  • [1] Metabolic rate in the right amygdala predicts negative affect in depressed patients
    Abercrombie, HC
    Schaefer, SM
    Larson, CL
    Oakes, TR
    Lindgren, KA
    Holden, JE
    Perlman, SB
    Turski, PA
    Krahn, DD
    Benca, RM
    Davidson, RJ
    [J]. NEUROREPORT, 1998, 9 (14) : 3301 - 3307
  • [2] The Bcl-2 protein family: Arbiters of cell survival
    Adams, JM
    Cory, S
    [J]. SCIENCE, 1998, 281 (5381) : 1322 - 1326
  • [3] SYNDROME PRODUCED BY LESIONS OF THE AMYGDALA IN MONKEYS (MACACA, MULATTA)
    AGGLETON, JP
    PASSINGHAM, RE
    [J]. JOURNAL OF COMPARATIVE AND PHYSIOLOGICAL PSYCHOLOGY, 1981, 95 (06): : 961 - 977
  • [4] An MRI study of temporal lobe structures in men with bipolar disorder or schizophrenia
    Altshuler, LL
    Bartzokis, G
    Grieder, T
    Curran, J
    Jimenez, T
    Leight, K
    Wilkins, J
    Gerner, R
    Mintz, J
    [J]. BIOLOGICAL PSYCHIATRY, 2000, 48 (02) : 147 - 162
  • [5] Amygdala enlargement in bipolar disorder and hippocampal reduction in schizophrenia: An MRI study demonstrating neuroanatomic specificity
    Altshuler, LL
    Bartzokis, G
    Grieder, T
    Curran, J
    Mintz, J
    [J]. ARCHIVES OF GENERAL PSYCHIATRY, 1998, 55 (07) : 663 - 664
  • [6] Amaral D.G., 1990, HUMAN NERVOUS SYSTEM, P711, DOI 10.1016/C2009-0-02721-4
  • [7] An X, 1998, J COMP NEUROL, V401, P455
  • [8] Dissociable neural responses to facial expressions of sadness and anger
    Blair, RJR
    Morris, JS
    Frith, CD
    Perrett, DI
    Dolan, RJ
    [J]. BRAIN, 1999, 122 : 883 - 893
  • [9] GLIAL-CELLS EXPRESS BOTH MINERALOCORTICOID AND GLUCOCORTICOID RECEPTORS
    BOHN, MC
    HOWARD, E
    VIELKIND, U
    KROZOWSKI, Z
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1991, 40 (1-3) : 105 - 111
  • [10] THE GLIAL-CELL GLUTAMATE UPTAKE CARRIER COUNTERTRANSPORTS PH-CHANGING ANIONS
    BOUVIER, M
    SZATKOWSKI, M
    AMATO, A
    ATTWELL, D
    [J]. NATURE, 1992, 360 (6403) : 471 - 474