Paroxetine can improve primary visual cortex activity in a high-risk mouse model of schizophrenia

Visual cortex functional deficits can be observed in schizophrenia patients and in individuals at high risk of schizophrenia. However, to date, few studies have investigated methods to improve these functional deficits. This study aimed to investigate the pathological change in the primary visual co...

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Main Authors: Xinying Chen, Ziyao Cai, Feng Ji, Xiaodong Lin, Deguo Jiang, Chongguang Lin, Xiaoyan Ma, Yong Xu, Wenqiang Wang, Lidan Zheng, Ce Chen, Chuanjun Zhuo
Format: Article
Language:English
Published: Taylor & Francis Group 2020-01-01
Series:Biotechnology & Biotechnological Equipment
Subjects:
Online Access:http://dx.doi.org/10.1080/13102818.2020.1837009
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spelling doaj-3e66e86129d745c18965da74024058e82020-12-07T14:56:59ZengTaylor & Francis GroupBiotechnology & Biotechnological Equipment1310-28181314-35302020-01-013411299130310.1080/13102818.2020.18370091837009Paroxetine can improve primary visual cortex activity in a high-risk mouse model of schizophreniaXinying Chen0Ziyao Cai1Feng Ji2Xiaodong Lin3Deguo Jiang4Chongguang Lin5Xiaoyan Ma6Yong Xu7Wenqiang Wang8Lidan Zheng9Ce Chen10Chuanjun Zhuo11Department of Psychiatric-Neuroimging-Genetics and Comorbidity Laboratory (PNGC_Lab), Tianjin Anding HospitalDepartment of Psychiatry and Micro-imaging Centre, Wenzhou Seventh People’s HospitalDepartment of Psychiatry, School of Mental Health, Jining Medical UniversityDepartment of Psychiatry and Micro-imaging Centre, Wenzhou Seventh People’s HospitalDepartment of Psychiatry and Micro-imaging Centre, Wenzhou Seventh People’s HospitalDepartment of Psychiatry and Micro-imaging Centre, Wenzhou Seventh People’s HospitalDepartment of Psychiatric-Neuroimging-Genetics and Comorbidity Laboratory (PNGC_Lab), Tianjin Anding HospitalDepartment of Psychiatry, First Hospital/First Clinical Medical College of Shanxi Medical UniversityCanada and China Joint Laboratory of Biological Psychiatry, Xiamen Xianye HospitalDepartment of Psychiatric-Neuroimging-Genetics and Comorbidity Laboratory (PNGC_Lab), Tianjin Anding HospitalDepartment of Psychiatric-Neuroimging-Genetics and Comorbidity Laboratory (PNGC_Lab), Tianjin Anding HospitalDepartment of Psychiatric-Neuroimging-Genetics and Comorbidity Laboratory (PNGC_Lab), Tianjin Anding HospitalVisual cortex functional deficits can be observed in schizophrenia patients and in individuals at high risk of schizophrenia. However, to date, few studies have investigated methods to improve these functional deficits. This study aimed to investigate the pathological change in the primary visual cortex of a prenatal MK-801-induced high-risk mouse model of schizophrenia (HRMMS) and to test the effect of paroxetine on visual cortex activity. Pregnant mice were given a systemic injection of MK-801, and male offspring that did not present schizophrenia-like behaviors in early adulthood were defined as HRMMS. Some of the HRMMS mice were treated with pharmacological agents beginning at 4 weeks of age. After 4 weeks of treatment with risperidone and/or paroxetine, two-photon calcium imaging was performed to analyze the primary visual cortex activity. The sucrose preference test and the prepulse inhibition (PPI) apparatus test were used to assess the cognitive and behavioral performance. HRMMS mice with or without risperidone treatment had impairments in the primary visual cortex as observed by reduced neuronal calcium activity. Risperidone plus paroxetine and paroxetine alone treatments increased the neuronal calcium activity in the primary visual cortex. Notably, the neuronal calcium activity was higher in mice treated with paroxetine alone. Treatment with paroxetine alone also improved the cognitive and behavioral performance better than treatment with risperidone plus paroxetine. Our pioneering animal model showed that treatment with paroxetine alone improves visual cortex impairments in HRMMS mice better than treatment with risperidone plus paroxetine, indicating that antipsychotics cannot normalize visual cortex impairments.http://dx.doi.org/10.1080/13102818.2020.1837009schizophreniaanimal modelprimary visual cortexrisperidone paroxetine
collection DOAJ
language English
format Article
sources DOAJ
author Xinying Chen
Ziyao Cai
Feng Ji
Xiaodong Lin
Deguo Jiang
Chongguang Lin
Xiaoyan Ma
Yong Xu
Wenqiang Wang
Lidan Zheng
Ce Chen
Chuanjun Zhuo
spellingShingle Xinying Chen
Ziyao Cai
Feng Ji
Xiaodong Lin
Deguo Jiang
Chongguang Lin
Xiaoyan Ma
Yong Xu
Wenqiang Wang
Lidan Zheng
Ce Chen
Chuanjun Zhuo
Paroxetine can improve primary visual cortex activity in a high-risk mouse model of schizophrenia
Biotechnology & Biotechnological Equipment
schizophrenia
animal model
primary visual cortex
risperidone
paroxetine
author_facet Xinying Chen
Ziyao Cai
Feng Ji
Xiaodong Lin
Deguo Jiang
Chongguang Lin
Xiaoyan Ma
Yong Xu
Wenqiang Wang
Lidan Zheng
Ce Chen
Chuanjun Zhuo
author_sort Xinying Chen
title Paroxetine can improve primary visual cortex activity in a high-risk mouse model of schizophrenia
title_short Paroxetine can improve primary visual cortex activity in a high-risk mouse model of schizophrenia
title_full Paroxetine can improve primary visual cortex activity in a high-risk mouse model of schizophrenia
title_fullStr Paroxetine can improve primary visual cortex activity in a high-risk mouse model of schizophrenia
title_full_unstemmed Paroxetine can improve primary visual cortex activity in a high-risk mouse model of schizophrenia
title_sort paroxetine can improve primary visual cortex activity in a high-risk mouse model of schizophrenia
publisher Taylor & Francis Group
series Biotechnology & Biotechnological Equipment
issn 1310-2818
1314-3530
publishDate 2020-01-01
description Visual cortex functional deficits can be observed in schizophrenia patients and in individuals at high risk of schizophrenia. However, to date, few studies have investigated methods to improve these functional deficits. This study aimed to investigate the pathological change in the primary visual cortex of a prenatal MK-801-induced high-risk mouse model of schizophrenia (HRMMS) and to test the effect of paroxetine on visual cortex activity. Pregnant mice were given a systemic injection of MK-801, and male offspring that did not present schizophrenia-like behaviors in early adulthood were defined as HRMMS. Some of the HRMMS mice were treated with pharmacological agents beginning at 4 weeks of age. After 4 weeks of treatment with risperidone and/or paroxetine, two-photon calcium imaging was performed to analyze the primary visual cortex activity. The sucrose preference test and the prepulse inhibition (PPI) apparatus test were used to assess the cognitive and behavioral performance. HRMMS mice with or without risperidone treatment had impairments in the primary visual cortex as observed by reduced neuronal calcium activity. Risperidone plus paroxetine and paroxetine alone treatments increased the neuronal calcium activity in the primary visual cortex. Notably, the neuronal calcium activity was higher in mice treated with paroxetine alone. Treatment with paroxetine alone also improved the cognitive and behavioral performance better than treatment with risperidone plus paroxetine. Our pioneering animal model showed that treatment with paroxetine alone improves visual cortex impairments in HRMMS mice better than treatment with risperidone plus paroxetine, indicating that antipsychotics cannot normalize visual cortex impairments.
topic schizophrenia
animal model
primary visual cortex
risperidone
paroxetine
url http://dx.doi.org/10.1080/13102818.2020.1837009
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