Article ; Online: Line- and sex-dependent effects of juvenile stress on contextual fear- and anxiety-related behavior in high- and low-alcohol-preferring mouse lines.
2024 Volume 463, Page(s) 114899
Abstract: Juvenile stress (JS) is a known risk factor for the development of alcohol use disorder (AUD) and post-traumatic stress disorder (PTSD), both of which are frequently co-morbid. Data suggest there may be common, genetically-influenced biological responses ...
| Abstract | Juvenile stress (JS) is a known risk factor for the development of alcohol use disorder (AUD) and post-traumatic stress disorder (PTSD), both of which are frequently co-morbid. Data suggest there may be common, genetically-influenced biological responses to stress that contribute to the development of both AUD and PTSD. The present study investigated the impact of JS on contextual fear learning and extinction, as well as corticosterone (CORT) responses before and after JS, before and after contextual fear conditioning (CFC), and after fear extinction in male and female high-alcohol-preferring (HAP2) and low-alcohol-preferring (LAP2) mouse lines. We also measured unconditioned anxiety-related behavior in the light-dark-transition test before CFC. HAP2 and LAP2 mice did not differ in fear acquisition, but HAP2 mice showed faster fear extinction compared to LAP2 mice. No effects of JS were seen in HAP2 mice, whereas in LAP2 mice, JS reduced fear acquisition in males and facilitated fear extinction in females. Females showed greater fear-related behavior relative to males, regardless of subgroup. HAP2 males demonstrated more anxiolytic-like responses than LAP2 males and LAP2 females demonstrated more anxiolytic-like responses than LAP2 males in the light-dark transition test. HAP2 and LAP2 mice did not differ in CORT during the juvenile stage; however, adult LAP2 mice showed greater CORT levels than HAP2 mice at baseline and after CFC and extinction testing. These findings build upon prior work in these unique mouse lines that differ in genetic propensity toward alcohol preference and provide new information regarding contextual fear learning and extinction mechanisms theorized to contribute to co-morbid AUD and PTSD. |
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| MeSH term(s) | Mice ; Female ; Male ; Animals ; Fear ; Anti-Anxiety Agents/pharmacology ; Extinction, Psychological ; Ethanol/pharmacology ; Alcoholism/genetics ; Anxiety |
| Chemical Substances | Anti-Anxiety Agents ; Ethanol (3K9958V90M) |
| Language | English |
| Publishing date | 2024-02-10 |
| Publishing country | Netherlands |
| Document type | Journal Article |
| ZDB-ID | 449927-x |
| ISSN | 1872-7549 ; 0166-4328 |
| ISSN (online) | 1872-7549 |
| ISSN | 0166-4328 |
| DOI | 10.1016/j.bbr.2024.114899 |
| Database | MEDical Literature Analysis and Retrieval System OnLINE |
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