Developing predictive animal models and establishing a preclinical trials network for assessing treatment effects on cognition in schizophrenia

被引:70
作者
Floresco, SB
Geyer, MA
Gold, LH
Grace, AA
机构
[1] Univ British Columbia, Dept Psychol, Vancouver, BC, Canada
[2] Univ Calif San Diego, Dept Psychiat, San Diego, CA 92103 USA
[3] Pfizer Global Res & Dev, CNS Mol Sci, Ann Arbor, MI USA
[4] Univ Pittsburgh, Dept Neurosci, Pittsburgh, PA USA
[5] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA USA
[6] Univ Pittsburgh, Dept Psychol, Pittsburgh, PA 15260 USA
关键词
MATRICS; antipsychotics; drug discovery;
D O I
10.1093/schbul/sbi041
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Animal models are an essential initial phase in the discovery of novel drugs to treat psychiatric disorders. At the sixth Measurement and Treatment Research to Improve Cognition in Schizophrenia conference, "New Approaches to Assessing and Improving Cognition in Schizophrenia," a discussion group was formed to address issues related to the development of predictive animal models of cognition that may be used as preclinical assays for putative cognitive enhancers. We identified 2 complementary approaches used to model cognitive impairments in animals. First, basic lesion/pharmacological models provide information about the particular neural substrates that may underlie different types of cognitive deficits found in schizophrenia. Findings from these studies can be mapped onto the second, more elaborate and etiologically relevant neurodevelopmental models of the disorder to ascertain which cognitive systems may be altered by early developmental insults. Particular attention must be given to the types of animal tasks used, in order to relate directly to the cognitive domains that are affected in schizophrenia patients. Importantly, the validation and standardization of the methodologies used in these preclinical assays would require the establishment of a preclinical trials network, serving as a counterpart to the recently established Treatment Units for Research on Neurocognition and Schizophrenia. The need to validate specific approaches to assess cognitive functions relevant to schizophrenia could be satisfied by a concerted effort enabled by a new funding directive from the National Institute of Mental Health with the explicit purpose of facilitating research on these models and assessing novel drug therapies that may be used to ameliorate the cognitive deficits in schizophrenia.
引用
收藏
页码:888 / 894
页数:7
相关论文
共 24 条
[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]   COGNITIVE DEFICIT CAUSED BY REGIONAL DEPLETION OF DOPAMINE IN PREFRONTAL CORTEX OF RHESUS-MONKEY [J].
BROZOSKI, TJ ;
BROWN, RM ;
ROSVOLD, HE ;
GOLDMAN, PS .
SCIENCE, 1979, 205 (4409) :929-932
[3]   6-HYDROXYDOPAMINE LESION OF THE RAT PREFRONTAL CORTEX INCREASES LOCOMOTOR-ACTIVITY, IMPAIRS ACQUISITION OF DELAYED ALTERNATION TASKS, BUT DOES NOT AFFECT UNINTERRUPTED TASKS IN THE RADIAL MAZE [J].
BUBSER, M ;
SCHMIDT, WJ .
BEHAVIOURAL BRAIN RESEARCH, 1990, 37 (02) :157-168
[4]   Dopaminergic modulation of visual attention and working memory in the rodent prefrontal cortex [J].
Chudasama, Y ;
Robbins, TW .
NEUROPSYCHOPHARMACOLOGY, 2004, 29 (09) :1628-1636
[5]  
Finkelstein JRJ, 1997, J ABNORM PSYCHOL, V106, P203
[6]   Disruption of neurogenesis on gestational day 17 in the rat causes behavioral changes relevant to positive and negative schizophrenia symptoms and alters amphetamine-induced dopamine release in nucleus accumbens [J].
Flagstad, P ;
Mork, A ;
Glenthoj, BY ;
van Beek, J ;
Michael-Titus, AT ;
Didriksen, M .
NEUROPSYCHOPHARMACOLOGY, 2004, 29 (11) :2052-2064
[7]   Delay-dependent modulation of memory retrieval by infusion of a dopamine D1 agonist into the rat medial prefrontal cortex [J].
Floresco, SB ;
Phillips, AG .
BEHAVIORAL NEUROSCIENCE, 2001, 115 (04) :934-939
[8]   Thalamic-cortical-striatal circuitry subserves working memory during delayed responding on a radial arm maze [J].
Floresco, SB ;
Braaksma, DN ;
Phillips, AG .
JOURNAL OF NEUROSCIENCE, 1999, 19 (24) :11061-11071
[9]   ISOLATION REARING OF RATS PRODUCES A DEFICIT IN PREPULSE INHIBITION OF ACOUSTIC STARTLE SIMILAR TO THAT IN SCHIZOPHRENIA [J].
GEYER, MA ;
WILKINSON, LS ;
HUMBY, T ;
ROBBINS, TW .
BIOLOGICAL PSYCHIATRY, 1993, 34 (06) :361-372
[10]   Targeting the dopamine D1 receptor in schizophrenia:: insights for cognitive dysfunction [J].
Goldman-Rakic, PS ;
Castner, SA ;
Svensson, TH ;
Siever, LJ ;
Williams, GV .
PSYCHOPHARMACOLOGY, 2004, 174 (01) :3-16