Neurotoxicity, neuroplasticity, and magnetic resonance imaging morphometry - What is happening in the schizophrenic brain?

被引:216
作者
Weinberger, DR [1 ]
McClure, RK [1 ]
机构
[1] NIMH, Clin Brain Disorders Branch, Intramural Res Program, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1001/archpsyc.59.6.553
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
In an era of dramatic discoveries in neuroscience and genetics, it is likely that many popular theories and formulations about mental illness will need to be revised, if not discarded. The "neurodevelopmental hypothesis" is one of the popular theories about the origins of schizophrenia, which posits that abnormalities of early brain development increase risk for the subsequent emergence of the clinical syndrome.(1-3) An early piece of evidence in support of this hypothesis was the apparent lack of progression of cerebral ventricular enlargement observed with computed tomography during illness.(4-9) An important assumption of the neuro developmental hypothesis is that the putative primary pathologic condition of the brain is a reflection of abnormalities of early development. The neuro developmental hypothesis thus assumes that developmental neuropathologic conditions should arrest early in life and not continue to progress. The computed tomography results showing no apparent progression seemed consistent with this assumption. However, a recent series of magnetic resonance imaging (MRI) studies has called into question this assumption, by revealing changes in measurements of brain structures over short periods in patients who have been ill for varying durations and at various stages of life. These recent studies'(10-14) have generated enthusiasm for a "neurodegenerative hypothesis," harkening back to proposals of Kraepelin and other neuropathologists during the first quarter of the 20th century that there is destruction of neural tissue associated with psychosis. In fact, results of MRI measurements have been cited as support for a much broader conceptual revolution in psychiatry, a "neurotoxicity hypothesis" for many psychiatric illnesses, including affective disorders(15,16) and anxiety and stress disorders(17-19) and even jet lag.(20) This recent trend has been bolstered by basic discoveries about the adaptability of neuronal connections(21) and the viability and reproducibility of neurons in the adult brain (eg, apoptosis and neurogenesis).(22,23) These developments have led some to opine that the neurodegenerative hypothesis of schizophrenia may have been unjustly overshadowed by the ascendancy of the neuro developmental hypothesis.(24)
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页码:553 / 558
页数:6
相关论文
共 76 条
  • [31] The neuropathology of schizophrenia - A critical review of the data and their interpretation
    Harrison, PJ
    [J]. BRAIN, 1999, 122 : 593 - 624
  • [32] Dexamethasone induces limited apoptosis and extensive sublethal damage to specific subregions of the striatum and hippocampus: Implications for mood disorders
    Haynes, LE
    Griffiths, MR
    Hyde, RE
    Barber, DJ
    Mitchell, IJ
    [J]. NEUROSCIENCE, 2001, 104 (01) : 57 - 69
  • [33] Apoptosis in the aging process
    Higami, Y
    Shimokawa, I
    [J]. CELL AND TISSUE RESEARCH, 2000, 301 (01) : 125 - 132
  • [34] 3-YEAR FOLLOW-UP OF OLDER SCHIZOPHRENICS - EXTRAPYRAMIDAL SYNDROMES, PSYCHIATRIC-SYMPTOMS, AND VENTRICULAR BRAIN RATIO
    HOFFMAN, WF
    BALLARD, L
    TURNER, EH
    CASEY, DE
    [J]. BIOLOGICAL PSYCHIATRY, 1991, 30 (09) : 913 - 926
  • [35] Honavar M, 1997, GREENFIELDS NEUROPAT, P931
  • [36] STABILITY OF CT SCAN FINDINGS IN SCHIZOPHRENIA - RESULTS OF AN 8 YEAR FOLLOW-UP-STUDY
    ILLOWSKY, BP
    JULIANO, DM
    BIGELOW, LB
    WEINBERGER, DR
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1988, 51 (02) : 209 - 213
  • [37] Progressive reduction of temporal lobe structures in childhood-onset schizophrenia
    Jacobsen, LK
    Giedd, JN
    Castellanos, FX
    Vaituzis, AC
    Hamburger, SD
    Kumra, S
    Lenane, MC
    Rapoport, JL
    [J]. AMERICAN JOURNAL OF PSYCHIATRY, 1998, 155 (05) : 678 - 685
  • [38] Cortical Bcl-2 protein expression and apoptotic regulation in schizophrenia
    Jarskog, LF
    Gilmore, JH
    Selinger, ES
    Lieberman, JA
    [J]. BIOLOGICAL PSYCHIATRY, 2000, 48 (07) : 641 - 650
  • [39] CEREBRAL VENTRICULAR ENLARGEMENT IN SCHIZOPHRENIFORM DISORDER DOES NOT PROGRESS - A 7 YEAR FOLLOW-UP-STUDY
    JASKIW, GE
    JULIANO, DM
    GOLDBERG, TE
    HERTZMAN, M
    UROWHAMELL, E
    WEINBERGER, DR
    [J]. SCHIZOPHRENIA RESEARCH, 1994, 14 (01) : 23 - 28
  • [40] KEMALI D, 1989, Biological Psychiatry, V26, P756, DOI 10.1016/0006-3223(89)90115-7