Aripiprazole, An Atypical Antipsychotic Drug, Improves Maturation and Complexity of Neuroblast Dendrites in the Mouse Dentate Gyrus Via Increasing Superoxide Dismutases
Apripiprazole (APZ) is well known as an atypical antipsychotic and antidepressant. In the present study, we investigated effects of APZ on cell proliferation and neuronal differentiation in the dentate gyrus (DG) of the adolescent mouse using BruU, Ki-67 and doublecortin (DCX) immunohistochemistry....
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Published in | Neurochemical research Vol. 38; no. 9; pp. 1980 - 1988 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Boston
Springer US
01.09.2013
Springer Nature B.V |
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Abstract | Apripiprazole (APZ) is well known as an atypical antipsychotic and antidepressant. In the present study, we investigated effects of APZ on cell proliferation and neuronal differentiation in the dentate gyrus (DG) of the adolescent mouse using BruU, Ki-67 and doublecortin (DCX) immunohistochemistry. BruU, Ki-67 and DCX-positive (+) cells were easily detected in the subgranular zone of the DG in the vehicle- and APZ-treated group. We found that in the 8 mg/kg APZ-treated group numbers of Ki-67
+
, DCX
+
and BrdU
+
/DCX
+
cells were significantly increased compared with those in the vehicle-treated group. We also found that maturation and complexity of DCX
+
dendrites in the 8 mg/kg APZ-treated group was well improved compared with those in the vehicle-treated group. In addition, markedly decreased lipid peroxidation and increased superoxide dismutase 2 (SOD2) level were observed in the DG of the 8 mg/kg APZ-treated group. Our present findings indicate that APZ can enhance cell proliferation and neuroblast differentiation, particularly maturation and complexity of neuroblast dendrites, in the DG via decreasing lipid peroxidation and increasing SOD2 level. |
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AbstractList | Apripiprazole (APZ) is well known as an atypical antipsychotic and antidepressant. In the present study, we investigated effects of APZ on cell proliferation and neuronal differentiation in the dentate gyrus (DG) of the adolescent mouse using BruU, Ki-67 and doublecortin (DCX) immunohistochemistry. BruU, Ki-67 and DCX-positive (+) cells were easily detected in the subgranular zone of the DG in the vehicle- and APZ-treated group. We found that in the 8 mg/kg APZ-treated group numbers of Ki-67^sup +^, DCX^sup +^ and BrdU^sup +^/DCX^sup +^ cells were significantly increased compared with those in the vehicle-treated group. We also found that maturation and complexity of DCX^sup +^ dendrites in the 8 mg/kg APZ-treated group was well improved compared with those in the vehicle-treated group. In addition, markedly decreased lipid peroxidation and increased superoxide dismutase 2 (SOD2) level were observed in the DG of the 8 mg/kg APZ-treated group. Our present findings indicate that APZ can enhance cell proliferation and neuroblast differentiation, particularly maturation and complexity of neuroblast dendrites, in the DG via decreasing lipid peroxidation and increasing SOD2 level.[PUBLICATION ABSTRACT] Apripiprazole (APZ) is well known as an atypical antipsychotic and antidepressant. In the present study, we investigated effects of APZ on cell proliferation and neuronal differentiation in the dentate gyrus (DG) of the adolescent mouse using BruU, Ki-67 and doublecortin (DCX) immunohistochemistry. BruU, Ki-67 and DCX-positive (+) cells were easily detected in the subgranular zone of the DG in the vehicle- and APZ-treated group. We found that in the 8 mg/kg APZ-treated group numbers of Ki-67(+), DCX(+) and BrdU(+)/DCX(+) cells were significantly increased compared with those in the vehicle-treated group. We also found that maturation and complexity of DCX(+) dendrites in the 8 mg/kg APZ-treated group was well improved compared with those in the vehicle-treated group. In addition, markedly decreased lipid peroxidation and increased superoxide dismutase 2 (SOD2) level were observed in the DG of the 8 mg/kg APZ-treated group. Our present findings indicate that APZ can enhance cell proliferation and neuroblast differentiation, particularly maturation and complexity of neuroblast dendrites, in the DG via decreasing lipid peroxidation and increasing SOD2 level. Apripiprazole (APZ) is well known as an atypical antipsychotic and antidepressant. In the present study, we investigated effects of APZ on cell proliferation and neuronal differentiation in the dentate gyrus (DG) of the adolescent mouse using BruU, Ki-67 and doublecortin (DCX) immunohistochemistry. BruU, Ki-67 and DCX-positive (+) cells were easily detected in the subgranular zone of the DG in the vehicle- and APZ-treated group. We found that in the 8 mg/kg APZ-treated group numbers of Ki-67 + , DCX + and BrdU + /DCX + cells were significantly increased compared with those in the vehicle-treated group. We also found that maturation and complexity of DCX + dendrites in the 8 mg/kg APZ-treated group was well improved compared with those in the vehicle-treated group. In addition, markedly decreased lipid peroxidation and increased superoxide dismutase 2 (SOD2) level were observed in the DG of the 8 mg/kg APZ-treated group. Our present findings indicate that APZ can enhance cell proliferation and neuroblast differentiation, particularly maturation and complexity of neuroblast dendrites, in the DG via decreasing lipid peroxidation and increasing SOD2 level. Apripiprazole (APZ) is well known as an atypical antipsychotic and antidepressant. In the present study, we investigated effects of APZ on cell proliferation and neuronal differentiation in the dentate gyrus (DG) of the adolescent mouse using BruU, Ki-67 and doublecortin (DCX) immunohistochemistry. BruU, Ki-67 and DCX-positive (+) cells were easily detected in the subgranular zone of the DG in the vehicle- and APZ-treated group. We found that in the 8 mg/kg APZ-treated group numbers of Ki-67 super(+), DCX super(+) and BrdU super(+)/DCX super(+) cells were significantly increased compared with those in the vehicle-treated group. We also found that maturation and complexity of DCX super(+) dendrites in the 8 mg/kg APZ-treated group was well improved compared with those in the vehicle-treated group. In addition, markedly decreased lipid peroxidation and increased superoxide dismutase 2 (SOD2) level were observed in the DG of the 8 mg/kg APZ-treated group. Our present findings indicate that APZ can enhance cell proliferation and neuroblast differentiation, particularly maturation and complexity of neuroblast dendrites, in the DG via decreasing lipid peroxidation and increasing SOD2 level. |
Author | Yan, Bing Chun Chen, Bai Hui Cho, Jun Hwi Park, Joon Ha Cho, Jeong-Hwi Lee, Jae-Chul Lee, Yun Lyul Kim, In Hye Kim, Sung Koo Won, Moo-Ho Lee, Dae Hwan Ahn, Ji Hyeon Lee, Bonghee |
Author_xml | – sequence: 1 givenname: Bai Hui surname: Chen fullname: Chen, Bai Hui organization: Department of Physiology, Institute of Neurodegeneration and Neuroregeneration, College of Medicine, Hallym University – sequence: 2 givenname: Bing Chun surname: Yan fullname: Yan, Bing Chun organization: Department of Neurobiology, School of Medicine, Kangwon National University, Institute of Integrative Traditional and Western Medicine, Medical College, Yangzhou University – sequence: 3 givenname: Joon Ha surname: Park fullname: Park, Joon Ha organization: Department of Neurobiology, School of Medicine, Kangwon National University – sequence: 4 givenname: Ji Hyeon surname: Ahn fullname: Ahn, Ji Hyeon organization: Laboratory of Neuroscience, Department of Physical Therapy, College of Rehabilitation Science, Daegu University – sequence: 5 givenname: Dae Hwan surname: Lee fullname: Lee, Dae Hwan organization: Laboratory of Neuroscience, Department of Physical Therapy, College of Rehabilitation Science, Daegu University – sequence: 6 givenname: In Hye surname: Kim fullname: Kim, In Hye organization: Department of Neurobiology, School of Medicine, Kangwon National University – sequence: 7 givenname: Jeong-Hwi surname: Cho fullname: Cho, Jeong-Hwi organization: Department of Neurobiology, School of Medicine, Kangwon National University – sequence: 8 givenname: Jae-Chul surname: Lee fullname: Lee, Jae-Chul organization: Department of Neurobiology, School of Medicine, Kangwon National University – sequence: 9 givenname: Sung Koo surname: Kim fullname: Kim, Sung Koo organization: Department of Pediatrics, School of Medicine, Dongtan Sacred Heart Hospital, Hallym University – sequence: 10 givenname: Bonghee surname: Lee fullname: Lee, Bonghee organization: Center for Genomics and Proteomics, Lee Gil Ya Cancer and Diabetes Institute, Gachon University of Medicine and Science – sequence: 11 givenname: Jun Hwi surname: Cho fullname: Cho, Jun Hwi organization: Department of Emergency Medicine, Institute of Medical Sciences, School of Medicine, Kangwon National University Hospital, Kangwon National University – sequence: 12 givenname: Moo-Ho surname: Won fullname: Won, Moo-Ho email: mhwon@kangwon.ac.kr organization: Department of Neurobiology, School of Medicine, Kangwon National University – sequence: 13 givenname: Yun Lyul surname: Lee fullname: Lee, Yun Lyul email: yylee@hallym.ac.kr organization: Department of Physiology, Institute of Neurodegeneration and Neuroregeneration, College of Medicine, Hallym University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23836293$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Adolescence Animals Antipsychotic Agents - pharmacology Aripiprazole Biochemistry Biomedical and Life Sciences Biomedicine Cell Biology Cell Differentiation - drug effects Cell Proliferation - drug effects Dentate Gyrus - cytology Dentate Gyrus - drug effects Dentate Gyrus - enzymology Male Mice Mice, Inbred ICR Neurochemistry Neurology Neurons - drug effects Neurosciences Original Paper Piperazines - pharmacology Quinolones - pharmacology Superoxide Dismutase - metabolism |
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Title | Aripiprazole, An Atypical Antipsychotic Drug, Improves Maturation and Complexity of Neuroblast Dendrites in the Mouse Dentate Gyrus Via Increasing Superoxide Dismutases |
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