| Literature DB >> 28798340 |
Jia-Hui Deng1,2, Wei Yan1,2,3, Ying Han4, Chen Chen2, Shi-Qiu Meng1, Cheng-Yu Sun1,2, Ling-Zhi Xu1,2, Yan-Xue Xue1, Xue-Jiao Gao1,2, Na Chen1, Fei-Long Zhang2, Yu-Mei Wang2,5, Jie Shi6, Lin Lu7,8,9.
Abstract
Early-life stress in adolescence has a long-lasting influence on brain function in adulthood, and it is mostly recognized as a predisposing factor for mental illnesses, such as anxiety and posttraumatic stress disorder. Previous studies also indicated that adolescent predictable chronic mild stress (PCMS) in early life promotes resilience to depression- and anxiety-like behaviors in adulthood. However, the role of PCMS in associated memory process is still unclear. In the present study, we found that adolescent PCMS facilitated extinction and inhibited fear response in reinstatement and spontaneous recovery tests in adult rats, and this effect was still present 1 week later. PCMS in adolescence increased the activity of brain-derived neurotrophic factor (BDNF)-extracellular signal-regulated kinase 1/2 (ERK1/2) signaling in infralimbic cortex (IL) but not prelimbic cortex in adulthood. Intra-IL infusion of BDNF antibody and the ERK1/2 inhibitor U0126 reversed PCMS-induced enhancement of fear extinction. Moreover, we found that PCMS decreased DNA methylation of the Bdnf gene at exons IV and VI and elevated the mRNA levels of Bdnf in the IL. Our findings indicate that adolescent PCMS exposure promotes fear memory extinction in adulthood, which reevaluates the traditional notion of adolescent stress.Entities:
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Year: 2017 PMID: 28798340 PMCID: PMC5552791 DOI: 10.1038/s41598-017-08017-7
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379