Molecular brain imaging and the neurobiology and genetics of schizophrenia

被引:0
|
作者
Heinz, A
Romero, B
Gallinat, J
Juckel, G
Weinberger, DR
机构
[1] Charite Univ Med Berlin, Dept Psychiat & Psychotherapy, D-10117 Berlin, Germany
[2] NIMH, Clin Brain Disorders Branch, NIH, Bethesda, MD 20892 USA
关键词
dopamine; PET; SPECT; fMRI; COMT genotype; neurodevelopment;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
It has been hypothesized that schizophrenia is related to dysfunction in temporolimbic-prefrontal neuronal networks, which is acquired early in an individual's development. After puberty, relatively reduced prefrontal control of striatal dopaminergic neurotransmission may lead to unmodulated striatal dopamine (DA) activity, and the positive symptoms of acute psychosis. Brain imaging studies support the notion of prefrontal dysfunction in schizophrenia and correlated upregulation of presynaptic striatal DA activity. Recent molecular brain imaging studies have combined genetic assessments with a multimodal neuroimaging approach to further refine our understanding of the pathophysiologic architecture of the disorder. We review the literature on functional brain imaging in schizophrenia and discuss genotype effects on core psychotic symptoms. A promising research strategy is the identification of genetic and environmental factors that contribute to intermediate phenotypes such as working memory deficits in schizophrenia. Molecular brain imaging can help to unravel the complex interactions between genes and environment and its association with neuronal network dysfunction in schizophrenia.
引用
收藏
页码:S152 / S157
页数:6
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