Prefrontal cortical network connections: key site of vulnerability in stress and schizophrenia

被引:123
作者
Arnsten, Amy F. T. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT 06510 USA
关键词
Prefrontal cortex; Catecholamines; Physiology; cAMP; DISC1; RGS4; Working memory; NICOTINIC ACETYLCHOLINE-RECEPTORS; PROTEIN SIGNALING 4; DENDRITIC SPINE MORPHOLOGY; 1ST EPISODE SCHIZOPHRENIA; WORKING-MEMORY; NMDA RECEPTORS; GRAY-MATTER; CORTEX; RGS4; ALPHA-7;
D O I
10.1016/j.ijdevneu.2011.02.006
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The symptoms of schizophrenia involve profound dysfunction of the prefrontal cortex (PFC). PFC networks create our "mental sketch pad", and PFC dysfunction contributes to symptoms such as cognitive deficits, thought disorder, delusions and hallucinations. Neuropathological studies of schizophrenia have shown marked loss of dendritic spines in deep layer III, the sublayer where PFC microcircuits reside. The microcircuits consist of recurrent excitatory pyramidal cell networks that interconnect on spines, and excite each other via NMDA receptor signaling. The pyramidal cell persistent firing is sculpted by lateral inhibition from GABAergic basket and chandelier cells, thus creating tuned, persistent firing needed for accurate representational knowledge (i.e., working memory). The strength of pyramidal cell network connections is markedly and flexibly altered by intracellular signaling pathways in dendritic spines, a process called dynamic network connectivity (DNC). DNC proteins such as HCN channels are concentrated on dendritic spines in deep layer III. Under optimal conditions, network inputs to pyramidal cells are strengthened by noradrenergic alpha-2A inhibition of cAMP-HCN channel signaling, and sculpted by dopamine D1-cAMP-HCN channel weakening of inappropriate inputs. However, with stress exposure, high levels of cAMP-HCN channel signaling produces a collapse in network firing. With chronic stress exposure, spines reduce in size and are lost, and this process involves increased PKC signaling. Importantly, molecules that normally strengthen PFC networks connections and/or reverse the stress response, are often genetically altered in schizophrenia. As exposure to stress is a key factor in the precipitation of schizophrenic symptoms, these dysregulated signaling pathways in deep layer III may interact with already vulnerable circuitry to cause spine loss and the descent into illness. (C) 2011 ISDN. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:215 / 223
页数:9
相关论文
共 113 条
[51]   Increased Synaptic Dopamine Function in Associative Regions of the Striatum in Schizophrenia [J].
Kegeles, Lawrence S. ;
Abi-Dargham, Anissa ;
Frankle, Gordon ;
Gil, Roberto ;
Cooper, Thomas B. ;
Slifstein, Mark ;
Hwang, Dah-Ren ;
Huang, Yiyun ;
Haber, Suzanne N. ;
Laruelle, Marc .
ARCHIVES OF GENERAL PSYCHIATRY, 2010, 67 (03) :231-239
[52]   A specific role for NR2A-containing NMDA receptors in the maintenance of parvalbumin and GAD67 immunoreactivity in cultured interneurons [J].
Kinney, JW ;
Davis, CN ;
Tabarean, I ;
Conti, B ;
Bartfai, T ;
Behrens, MM .
JOURNAL OF NEUROSCIENCE, 2006, 26 (05) :1604-1615
[53]   DISC1 immunoreactivity at the light and ultrastructural level in the human neocortex [J].
Kirkpatrick, Brian ;
Xu, Leyan ;
Cascella, Nicola ;
Ozeki, Yuji ;
Sawa, Akira ;
Roberts, Rosalinda C. .
JOURNAL OF COMPARATIVE NEUROLOGY, 2006, 497 (03) :436-450
[54]  
KNIGHT RT, 1995, ADV NEUROL, V66, P21
[55]   Expression of the NR2B-NMDA Receptor Subunit and Its Tbr-1/CINAP Regulatory Proteins in Postmortem Brain Suggest Altered Receptor Processing in Schizophrenia [J].
Kristiansen, Lars V. ;
Patel, Sagar A. ;
Haroutunian, Vahram ;
Meador-Woodruff, James H. .
SYNAPSE, 2010, 64 (07) :495-502
[56]   INTRINSIC CIRCUIT ORGANIZATION OF THE MAJOR LAYERS AND SUBLAYERS OF THE DORSOLATERAL PREFRONTAL CORTEX IN THE RHESUS-MONKEY [J].
KRITZER, MF ;
GOLDMANRAKIC, PS .
JOURNAL OF COMPARATIVE NEUROLOGY, 1995, 359 (01) :131-143
[57]   Dopamine increases inhibition in the monkey dorsolateral prefrontal cortex through cell type-specific modulation of interneurons [J].
Kroner, Sven ;
Krimer, Leonid S. ;
Lewis, David A. ;
Barrionuevo, German .
CEREBRAL CORTEX, 2007, 17 (05) :1020-1032
[58]   NMDA receptor antagonist effects, cortical glutamatergic function, and schizophrenia: toward a paradigm shift in medication development [J].
Krystal, JH ;
D'Souza, DC ;
Mathalon, D ;
Perry, E ;
Belger, A ;
Hoffman, R .
PSYCHOPHARMACOLOGY, 2003, 169 (3-4) :215-233
[59]   Single photon emission computerized tomography imaging of amphetamine-induced dopamine release in drug-free schizophrenic subjects [J].
Laruelle, M ;
Abi-Dargham, A ;
vanDyck, CH ;
Gil, R ;
DSouza, CD ;
Erdos, J ;
McCance, E ;
Rosenblatt, W ;
Fingado, C ;
Zoghbi, SS ;
Baldwin, RM ;
Seibyl, JP ;
Krystal, JH ;
Charney, DS ;
Innis, RB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (17) :9235-9240
[60]   Functional specialization of the primate frontal cortex during decision making [J].
Lee, Daeyeol ;
Rushworth, Matthew F. S. ;
Walton, Mark E. ;
Watanabe, Masataka ;
Sakagami, Masamichi .
JOURNAL OF NEUROSCIENCE, 2007, 27 (31) :8170-8173