Schizophrenia, "just the facts": What we know in 2008 Part 3: Neurobiology

被引:229
作者
Keshavan, Matcheri S. [1 ,2 ]
Tandon, Rajiv [3 ]
Boutros, Nash N. [1 ]
Nasrallah, Henry A. [4 ]
机构
[1] Wayne State Univ, Sch Med, Dept Psychiat & Behav Neurosci, Detroit, MI 48202 USA
[2] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Psychiat, Boston, MA 02215 USA
[3] Univ Florida, Dept Psychiat, Gainesville, FL 32611 USA
[4] Univ Cincinnati, Coll Med, Dept Psychiat, Cincinnati, OH USA
关键词
Chemistry; Electrophysiology; Endophenotype; Imaging; Neurobiology; Pathology; Pharmacology; Physiology; Schizophrenia;
D O I
10.1016/j.schres.2008.07.020
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Investigating the neurobiological basis of schizophrenia is a critical step toward establishing its diagnostic validity, predicting outcome, delineating causative mechanisms and identifying objective targets for treatment research. Over the past two decades, there have been several advances in this field, principally related to developments in neuroimaging, electrophysiological and neuropathological approaches. Several neurobiological alterations in domains of brain structure, physiology and neurochemistry have been documented that may reflect diverse pathophysiological pathways from the "genome to the phenome". While none of the observed abnormalities are likely to qualify as diagnostic markers at this time, many can serve as potential intermediate phenotypes for elucidating etiological factors including susceptibility genes, and as therapeutic targets for novel drug discovery. Despite several challenges including the substantial phenotypic, pathophysiologic and etiological heterogeneity of schizophrenia, technological limitations, and the less than ideal animal models, considerable progress has been made in characterizing the neurobiological substrate of schizophrenia. The accumulating fact-base on the neurobiology of schizophrenia calls for novel integrative model(s) that may generate new, testable predictions. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:89 / 107
页数:19
相关论文
共 243 条
[1]   What have we learned from proton magnetic resonance spectroscopy about schizophrenia? A critical update [J].
Abbott, C ;
Bustillo, J .
CURRENT OPINION IN PSYCHIATRY, 2006, 19 (02) :135-139
[2]   Prefrontal dopamine D1 receptors and working memory in schizophrenia [J].
Abi-Dargham, A ;
Mawlawi, O ;
Lombardo, I ;
Gil, R ;
Martinez, D ;
Huang, YY ;
Hwang, DR ;
Keilp, J ;
Kochan, L ;
Van Heertum, R ;
Gorman, JM ;
Laruelle, M .
JOURNAL OF NEUROSCIENCE, 2002, 22 (09) :3708-3719
[3]   Alterations of serotonin transmission in schizophrenia [J].
Abi-Dargham, Anissa .
INTEGRATING THE NEUROBIOLOGY OF SCHIZOPHRENIA, 2007, 78 :133-164
[4]   Episodic memory-related activation in schizophrenia: meta-analysis [J].
Achim, AM ;
Lepage, M .
BRITISH JOURNAL OF PSYCHIATRY, 2005, 187 :500-509
[5]  
AKBARIAN S, 1993, ARCH GEN PSYCHIAT, V50, P169
[6]   A unitary model of schizophrenia -: Bleuler's "fragmented phrene" as schizencephaly [J].
Andreasen, NC .
ARCHIVES OF GENERAL PSYCHIATRY, 1999, 56 (09) :781-787
[7]   Genetic influences on prepulse inhibition of startle reflex in humans [J].
Anokhin, AP ;
Heath, AC ;
Myers, E ;
Ralano, A ;
Wood, S .
NEUROSCIENCE LETTERS, 2003, 353 (01) :45-48
[8]   The relationship between brain structure and neurocognition in schizophrenia: a selective review [J].
Antonova, E ;
Sharma, T ;
Morris, R ;
Kumari, V .
SCHIZOPHRENIA RESEARCH, 2004, 70 (2-3) :117-145
[9]   Modeling madness in mice: One piece at a time [J].
Arguello, P. Alexander ;
Gogos, Joseph A. .
NEURON, 2006, 52 (01) :179-196
[10]   Neurodevelopment, neuroplasticity, and new genes for schizophrenia [J].
Arnold, SE ;
Talbot, K ;
Hahn, CG .
DEVELOPMENT, DYNAMICS AND PATHOLOGY OF NEURONAL NETWORKS: FROM MOLECULES TO FUNCTIONAL CIRCUITS, 2005, 147 :319-345