TY - JOUR
T1 - Impact of brain-behavior phenotypying of genetically-engineered mice on research of neuropsychiatric disorders
AU - Takao, Keizo
AU - Yamasaki, Nobuyuki
AU - Miyakawa, Tsuyoshi
N1 - Funding Information:
This work was supported by Grant-in-Aid for Young Scientists (A) (#16680015), Grant-in-Aid for Exploratory Research (#16653065), Grant-in-Aid for Scientific Research on Priority Areas (#18023022, #18016012 and #18053015) from Ministry of Education, Culture, Sports, Science and Technology in Japan, National Alliance for Research on Schizophrenia and Depression (NARSD), Grant-in-Aid from Promotion of Fundamental Studies in Health Sciences of the National Institute of Biomedical Innovation (NIBIO), Grant-in-Aid from Neuroinformatics Japan Center (NIJC), RIKEN, and Grant-in-Aid from Institute for Bioinformatics Research and Development (BIRD) of Japan Science and Technology Agency.
PY - 2007/6
Y1 - 2007/6
N2 - Despite massive research efforts, the exact pathogenesis and pathophysiology of psychiatric disorders, such as schizophrenia and bipolar disorder, remain largely unknown. Animal models can serve as essential tools for investigating the etiology and treatment of such disorders. Since the introduction of gene targeting techniques, the functions of more than 10% of all known mouse genes have been investigated by creating mutant mice. Some of these mutant mouse strains were found to exhibit behavioral abnormalities reminiscent of human psychiatric disorders. In this review, we discuss the general requirements for animal models of human psychiatric disorders. We also outline our unique approach of extrapolating findings in mice to humans, and present studies on forebrain-specific calcineurin knockout mice as an example. We also discuss the impact of a large-scale mouse phenotyping on studies of psychiatric disorders and the potential utility of an "animal-model-array" of psychiatric disorders for the development of suitable therapeutic agents.
AB - Despite massive research efforts, the exact pathogenesis and pathophysiology of psychiatric disorders, such as schizophrenia and bipolar disorder, remain largely unknown. Animal models can serve as essential tools for investigating the etiology and treatment of such disorders. Since the introduction of gene targeting techniques, the functions of more than 10% of all known mouse genes have been investigated by creating mutant mice. Some of these mutant mouse strains were found to exhibit behavioral abnormalities reminiscent of human psychiatric disorders. In this review, we discuss the general requirements for animal models of human psychiatric disorders. We also outline our unique approach of extrapolating findings in mice to humans, and present studies on forebrain-specific calcineurin knockout mice as an example. We also discuss the impact of a large-scale mouse phenotyping on studies of psychiatric disorders and the potential utility of an "animal-model-array" of psychiatric disorders for the development of suitable therapeutic agents.
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U2 - 10.1016/j.neures.2007.02.009
DO - 10.1016/j.neures.2007.02.009
M3 - Article
C2 - 17524507
AN - SCOPUS:34249719431
SN - 0168-0102
VL - 58
SP - 124
EP - 132
JO - Neuroscience Research
JF - Neuroscience Research
IS - 2
ER -