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      Comprehensive behavioral analysis of pituitary adenylate cyclase-activating polypeptide (PACAP) knockout mice

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          Abstract

          Pituitary adenylate cyclase-activating polypeptide (PACAP) is a neuropeptide acting as a neurotransmitter, neuromodulator, or neurotrophic factor. PACAP is widely expressed throughout the brain and exerts its functions through the PACAP-specific receptor (PAC 1). Recent studies reveal that genetic variants of the PACAP and PAC 1 genes are associated with mental disorders, and several behavioral abnormalities of PACAP knockout (KO) mice are reported. However, an insufficient number of backcrosses was made using PACAP KO mice on the C57BL/6J background due to their postnatal mortality. To elucidate the effects of PACAP on neuropsychiatric function, the PACAP gene was knocked out in F1 hybrid mice (C57BL/6J × 129SvEv) for appropriate control of the genetic background. The PACAP KO mice were then subjected to a behavioral test battery. PACAP deficiency had no significant effects on neurological screen. As shown previously, the mice exhibited significantly increased locomotor activity in a novel environment and abnormal anxiety-like behavior, while no obvious differences between genotypes were shown in home cage (HC) activity. In contrast to previous reports, the PACAP KO mice showed normal prepulse inhibition (PPI) and slightly decreased depression-like behavior. Previous study demonstrates that the social interaction (SI) in a resident-intruder test was decreased in PACAP KO mice. On the other hand, we showed that PACAP KO mice exhibited increased SI in Crawley's three-chamber social approach test, although PACAP KO had no significant impact on SI in a HC. PACAP KO mice also exhibited mild performance deficit in working memory in an eight-arm radial maze (RM) and the T-maze (TM), while they did not show any significant abnormalities in the left-right discrimination task in the TM. These results suggest that PACAP has an important role in the regulation of locomotor activity, social behavior, anxiety-like behavior and, potentially, working memory.

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          Genetics of mouse behavior: interactions with laboratory environment.

          Strains of mice that show characteristic patterns of behavior are critical for research in neurobehavioral genetics. Possible confounding influences of the laboratory environment were studied in several inbred strains and one null mutant by simultaneous testing in three laboratories on a battery of six behaviors. Apparatus, test protocols, and many environmental variables were rigorously equated. Strains differed markedly in all behaviors, and despite standardization, there were systematic differences in behavior across labs. For some tests, the magnitude of genetic differences depended upon the specific testing lab. Thus, experiments characterizing mutants may yield results that are idiosyncratic to a particular laboratory.
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            Neuroscience of attention-deficit/hyperactivity disorder: the search for endophenotypes.

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              Post-traumatic stress disorder is associated with PACAP and the PAC1 receptor

              Pituitary adenylate cyclase-activating polypeptide (PACAP) is known to broadly regulate the cellular stress response. In contrast, it is unclear if the PACAP/PAC1 receptor pathway has a role in human psychological stress responses, such as posttraumatic stress disorder (PTSD). In heavily traumatized subjects, we find a sex-specific association of PACAP blood levels with fear physiology, PTSD diagnosis and symptoms in females (N=64, replication N=74, p<0.005). Using a tag-SNP genetic approach (44 single nucleotide polymorphisms, SNPs) spanning the PACAP (ADCYAP1) and PAC1 (ADCYAP1R1) genes, we find a sex-specific association with PTSD. rs2267735, a SNP in a putative estrogen response element within ADCYAP1R1, predicts PTSD diagnosis and symptoms in females only (combined initial and replication samples: N=1237; p<2x10 − 5). This SNP also associates with fear discrimination and with ADCYAP1R1 mRNA expression. Methylation of ADCYAP1R1 is also associated with PTSD (p < 0.001). Complementing these human data, ADCYAP1R1 mRNA is induced with fear conditioning or estrogen replacement in rodent models. These data suggest that perturbations in the PACAP/PAC1 pathway are involved in abnormal stress responses underlying PTSD. These sex-specific effects may occur via estrogen regulation of ADCYAP1R1. PACAP levels and ADCYAP1R1 SNPs may serve as useful biomarkers to further our mechanistic understanding of PTSD.
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                Author and article information

                Journal
                Front Behav Neurosci
                Front Behav Neurosci
                Front. Behav. Neurosci.
                Frontiers in Behavioral Neuroscience
                Frontiers Media S.A.
                1662-5153
                02 October 2012
                2012
                : 6
                : 58
                Affiliations
                [1] 1simpleDivision of Systems Medical Science, Institute for Comprehensive Medical Science, Fujita Health University Toyoake, Aichi, Japan
                [2] 2simpleJapan Science and Technology Agency, Core Research for Evolutional Science and Technology Kawaguchi, Saitama, Japan
                [3] 3simpleCenter for Genetic Analysis of Behavior, National Institute for Physiological Sciences Okazaki, Aichi, Japan
                [4] 4simpleGenetic Engineering and Functional Genomics Group, Frontier Technology Center, Graduate School of Medicine, Kyoto University Kyoto, Kyoto, Japan
                [5] 5simpleDepartment of Pediatrics, Kyoto Prefectural University of Medicine Kyoto, Kyoto, Japan
                [6] 6simpleLaboratory of Molecular Neuropharmacology, Graduate School of Pharmaceutical Sciences, Osaka University Suita, Osaka, Japan
                [7] 7simpleUnited Graduate School of Child Development, Osaka University, Kanazawa University and Hamamatsu University School of Medicine Suita, Osaka, Japan
                Author notes

                Edited by: Carmen Sandi, École Polytechnique Fédérale de Lausanne, Switzerland

                Reviewed by: Osborne F. Almeida, University of Minho, Portugal; Alessandro Bartolomucci, University of Minnesota, USA

                *Correspondence: Tsuyoshi Miyakawa, Division of Systems Medical Science, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo Kutsukake-cho, Toyoake, Aichi 470-1192, Japan. e-mail: miyakawa@ 123456fujita-hu.ac.jp

                †Present Address: Akemichi Baba, School of Pharmacy, Hyogo University of Health Sciences, Kobe, Hyogo, Japan.

                Article
                10.3389/fnbeh.2012.00058
                3462416
                23060763
                fe7fbdb4-25b3-40ac-a7a9-b125d15b8320
                Copyright © 2012 Hattori, Takao, Tanda, Toyama, Shintani, Baba, Hashimoto and Miyakawa.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

                History
                : 14 June 2012
                : 22 August 2012
                Page count
                Figures: 6, Tables: 2, Equations: 0, References: 58, Pages: 18, Words: 13525
                Categories
                Neuroscience
                Original Research Article

                Neurosciences
                mental disorder,hyperactivity,pituitary adenylate cyclase-activating polypeptide,behavior,social interaction,knockout mouse,working memory

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