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Aripiprazole, An Atypical Antipsychotic Drug, Improves Maturation and Complexity of Neuroblast Dendrites in the Mouse Dentate Gyrus Via Increasing Superoxide Dismutases

Authors
Chen, Bai HuiYan, Bing ChunPark, Joon HaAhn, Ji HyeonLee, Dae HwanKim, In HyeCho, Jeong-HwiLee, Jae-ChulKim, Sung KooLee, BongheeCho, Jun HwiWon, Moo-HoLee, Yun Lyul
Issue Date
Sep-2013
Publisher
SPRINGER/PLENUM PUBLISHERS
Keywords
Atypical antipsychotic; Neurogenesis; Cell proliferation; Neuroblast differentiation; Antioxidants
Citation
NEUROCHEMICAL RESEARCH, v.38, no.9, pp.1980 - 1988
Journal Title
NEUROCHEMICAL RESEARCH
Volume
38
Number
9
Start Page
1980
End Page
1988
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/14327
DOI
10.1007/s11064-013-1104-2
ISSN
0364-3190
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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