Please use this identifier to cite or link to this item: https://doi.org/10.1177/1559325818822574
Title: THE DISPARITY OF IMPAIRMENT OF NEUROGENESIS AND COGNITION AFTER ACUTE OR FRACTIONATED RADIATION EXPOSURE IN ADOLESCENT BALB/C MICE
Authors: Peng, S
Yang, B
Duan, MY
Liu, ZW
Wang, WF
Zhang, XZ
Ren, BX
Tang, FR 
Keywords: Acute or fractionated irradiation
cognition
interneurons
neurogenesis
Issue Date: 1-Jan-2019
Publisher: SAGE Publications
Citation: Peng, S, Yang, B, Duan, MY, Liu, ZW, Wang, WF, Zhang, XZ, Ren, BX, Tang, FR (2019-01-01). THE DISPARITY OF IMPAIRMENT OF NEUROGENESIS AND COGNITION AFTER ACUTE OR FRACTIONATED RADIATION EXPOSURE IN ADOLESCENT BALB/C MICE 17 (1) : 1559325818822574-. ScholarBank@NUS Repository. https://doi.org/10.1177/1559325818822574
Abstract: © The Author(s) 2019. The effect of acute X-ray irradiation with 2 Gy or fractionated exposure with 0.2 Gy continuously for 10 days (0.2 Gy × 10 = 2 Gy) was evaluated in the postnatal day 21 (P21) BALB/c mouse model. Both acute and fractionated irradiation induced impairment of cell proliferation and neurogenesis in the subgranular zone of the dentate gyrus labeled by Ki67 and doublecortin, respectively. Parvalbumin immunopositive interneurons in the subgranular zone were also reduced significantly. However, the 2 patterns of irradiation did not affect animal weight gain when measured at ages of P90 and P180 or 69 and 159 days after irradiation. Behavioral tests indicated that neither acute nor fractionated irradiation with a total dose of 2 Gy induced deficits in the contextual fear or spatial memory and memory for novel object recognition. Animal motor activity was also not affected in the open-field test. The disparity of the impairment of neurogenesis and unaffected cognition suggests that the severity of impairment of neurogenesis induced by acute or fractionated irradiation with a total dose of 2 Gy at P21 may not be worse enough to induce the deficit of cognition.
URI: https://scholarbank.nus.edu.sg/handle/10635/155264
ISSN: 1559-3258
1559-3258
DOI: 10.1177/1559325818822574
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