Up-regulation of the D1 dopamine receptor-interacting protein, calcyon, in patients with schizophrenia

被引:63
作者
Koh, PO
Bergson, C
Undie, AS
Goldman-Rakic, PS
Lidow, MS
机构
[1] Univ Maryland, Dept Oral & Craniofacial Biol Sci, Baltimore, MD 21201 USA
[2] Univ Maryland, Dept Pharmaceut Sci, Baltimore, MD 21201 USA
[3] Med Coll Georgia, Dept Pharmacol & Toxicol, Augusta, GA 30912 USA
[4] Yale Univ, Dept Neurobiol, New Haven, CT USA
关键词
D O I
10.1001/archpsyc.60.3.311
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: The dopamine hypothesis remains a prominent influence on research into the pathogenesis of schizophrenia, yet the presence of consistent schizophrenia-linked abnormalities in the presynaptic components of the dopamine system or in dopamine receptors still remains a matter of debate. The present study focuses on a recently recognized group of dopamine receptor-interacting proteins as possible novel sites of dysfunction in schizophrenia. Specifically, we examined whether the D I dopamine receptor-interacting protein calcyon and the D2 dopamine receptor-interacting proteins filamin-A and spinophilin are affected in the dorsolateral prefrontal cortex of patients with schizophrenia. Methods: Slot blots of dorsolateral prefrontal cortical tissue were used to compare the levels of the 3 proteins of interest in control, schizophrenic, bipolar, and major depression groups (n = 15 per group). The nonschizophrenic psychiatric groups were included to determine the specificity of the detected abnormalities. Results: The dorsolateral prefrontal cortex in schizophrenic patients displayed nearly twice the normal levels of calcyon, whereas filamin-A and spinophilin levels were unaltered. Patients with bipolar disorder or major depression showed no changes in all 3 proteins examined. Conclusion: Our findings provide the first evidence that abnormalities in the dopamine system of patients with schizophrenia may lie in altered levels of dopamine receptor-interacting proteins.
引用
收藏
页码:311 / 319
页数:9
相关论文
共 58 条
[1]  
AAKHUS AM, 1992, THROMB HAEMOSTASIS, V67, P252
[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]   Spinophilin, a novel protein phosphatase 1 binding protein localized to dendritic spines [J].
Allen, PB ;
Ouimet, CC ;
Greengard, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (18) :9956-9961
[4]  
[Anonymous], 1991, HDB PSYCHIAT DRUG TH
[5]   DOPAMINE D-1 RECEPTOR MECHANISMS IN THE COGNITIVE PERFORMANCE OF YOUNG-ADULT AND AGED MONKEYS [J].
ARNSTEN, AFT ;
CAI, JX ;
MURPHY, BL ;
GOLDMANRAKIC, PS .
PSYCHOPHARMACOLOGY, 1994, 116 (02) :143-151
[6]   Monoaminergic synapses and schizophrenia: 45 years of neuroleptics [J].
Bennett, MR .
JOURNAL OF PSYCHOPHARMACOLOGY, 1998, 12 (03) :289-304
[7]  
Birnbaum S. G., 2001, Society for Neuroscience Abstracts, V27, P1404
[8]  
BRODMANN K, 1994, LCOALIZATION CEREBRA
[9]   Evidence for a compromised dorsolateral prefrontal cortical parallel circuit in schizophrenia [J].
Bunney, WE ;
Bunney, BG .
BRAIN RESEARCH REVIEWS, 2000, 31 (2-3) :138-146
[10]   Reversal of antipsychotic-induced working memory deficits by short-term doper D1 receptor stimulation [J].
Castner, SA ;
Williams, GV ;
Goldman-Rakic, PS .
SCIENCE, 2000, 287 (5460) :2020-2022