Dopamine receptor signaling molecules are altered in elderly schizophrenic cortex

被引:45
作者
Baracskay, Karen L.
Haroutunian, Vahram
Meador-Woodruff, James H.
机构
[1] Univ Michigan, Mol & Behav Neurosci Inst, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Psychiat, Ann Arbor, MI 48109 USA
[3] Mt Sinai Sch Med, Dept Psychiat, New York, NY USA
关键词
calcyon; spinophilin; DARPP-32; dorsolateral prefrontal cortex; anterior cingulate cortex;
D O I
10.1002/syn.20292
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Alterations of molecules that mediate dopaminergic signal transduction have been found in schizophrenia, supporting the hypothesis of altered dopaminergic neurotransmission in this illness. To further explore this hypothesis, the authors measured transcript expression of three proteins involved in dopamine (DA) signaling in postmortem dorsolateral prefrontal and anterior cingulate cortex of elderly schizophrenic subjects and a comparison group. The transcript encoding calcyon, a protein that potentiates crosstalk between D1 DA receptors and G(q/11)-linked receptors, was increased in schizophrenic prefrontal and cingulate cortex by 25%. Transcript levels of spinophilin, a protein enriched in dendritic spines that modulates excitatory neurotransmission, were increased 22% in dorsolateral prefrontal cortex but were unchanged in anterior cingulate cortex in schizophrenia. Levels of DARPP-32 mRNA, a downstream effector of dopaminergic neurotransmission, were similar in both groups for both cortical groups. These alterations in spinophilin and calcyon mRNA levels in schizophrenic prefrontal and cingulate cortex provide further evidence of altered dopaminergic neurotransmission in this illness.
引用
收藏
页码:271 / 279
页数:9
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[1]
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
[2]
Evidence for decreased DARPP-32 in the prefrontal cortex of patients with schizophrenia [J].
Albert, KA ;
Hemmings, HC ;
Adamo, AIB ;
Potkin, SG ;
Akbarian, S ;
Sandman, CA ;
Cotman, CW ;
Bunney, WE ;
Greengard, P .
ARCHIVES OF GENERAL PSYCHIATRY, 2002, 59 (08) :705-712
[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]
Abnormalities in the dopamine system in schizophrenia may lie in altered levels of dopamine receptor-interacting proteins [J].
Bai, J ;
He, F ;
Novikova, SI ;
Undie, AS ;
Dracheva, S ;
Haroutunian, V ;
Lidow, MS .
BIOLOGICAL PSYCHIATRY, 2004, 56 (06) :427-440
[5]
Emerging principles of altered neural circuitry in schizophrenia [J].
Benes, FM .
BRAIN RESEARCH REVIEWS, 2000, 31 (2-3) :251-269
[6]
Monoaminergic synapses and schizophrenia: 45 years of neuroleptics [J].
Bennett, MR .
JOURNAL OF PSYCHOPHARMACOLOGY, 1998, 12 (03) :289-304
[7]
DARPP-32, A PHOSPHOPROTEIN ENRICHED IN DOPAMINOCEPTIVE NEURONS BEARING DOPAMINE D1 RECEPTORS - DISTRIBUTION IN THE CEREBRAL-CORTEX OF THE NEWBORN AND ADULT RHESUS-MONKEY [J].
BERGER, B ;
FEBVRET, A ;
GREENGARD, P ;
GOLDMANRAKIC, PS .
JOURNAL OF COMPARATIVE NEUROLOGY, 1990, 299 (03) :327-348
[8]
EXPRESSION OF MESSENGER-RNAS ENCODING ARPP-16/19, ARPP-21, AND DARPP-32 IN HUMAN BRAIN-TISSUE [J].
BRENE, S ;
LINDEFORS, N ;
EHRLICH, M ;
TAUBES, T ;
HORIUCHI, A ;
KOPP, J ;
HALL, H ;
SEDVALL, G ;
GREENGARD, P ;
PERSSON, H .
JOURNAL OF NEUROSCIENCE, 1994, 14 (03) :985-998
[9]
DISTRIBUTION OF MESSENGER-RNAS FOR D-1 DOPAMINE-RECEPTORS AND DARPP-32 IN STRIATUM AND CEREBRAL-CORTEX OF THE CYNOMOLGUS MONKEY - RELATIONSHIP TO D-1 DOPAMINE-RECEPTORS [J].
BRENE, S ;
HALL, H ;
LINDEFORS, N ;
KARLSSON, P ;
HALLDIN, C ;
SEDVALL, G .
NEUROSCIENCE, 1995, 67 (01) :37-48
[10]
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