3004 Effects of Early Life Stress on Adult Behavioral and Neural Outcomes in Rats

OBJECTIVES/SPECIFIC AIMS: Early life stress is known to greatly impact neurodevelopment during critical periods, conferring risk for various psychopathologies, including the onset and exacerbation of schizophrenia and anxiety disorders. The endocannabinoid system is highly integrated into the stress...

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Main Authors: Alexandra Moussa-Tooks, Ken Mackie, John Green, Lisa Bartolomeo, Alex Gimeno, Eric Larson, Heather Bradshaw, Emma Leishman, Brian O’Donnell, William Hetrick
Format: Article
Language:English
Published: Cambridge University Press 2019-03-01
Series:Journal of Clinical and Translational Science
Online Access:https://www.cambridge.org/core/product/identifier/S2059866119000268/type/journal_article
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author Alexandra Moussa-Tooks
Ken Mackie
John Green
Lisa Bartolomeo
Alex Gimeno
Eric Larson
Heather Bradshaw
Emma Leishman
Brian O’Donnell
William Hetrick
author_facet Alexandra Moussa-Tooks
Ken Mackie
John Green
Lisa Bartolomeo
Alex Gimeno
Eric Larson
Heather Bradshaw
Emma Leishman
Brian O’Donnell
William Hetrick
author_sort Alexandra Moussa-Tooks
collection DOAJ
description OBJECTIVES/SPECIFIC AIMS: Early life stress is known to greatly impact neurodevelopment during critical periods, conferring risk for various psychopathologies, including the onset and exacerbation of schizophrenia and anxiety disorders. The endocannabinoid system is highly integrated into the stress response and may be one means by which early life stress produces such deleterious effects. Using a naturalistic, ecologically valid animal model, this study explored interactions between the stress response and endocannabinoid systems within the cerebellum, a region dense with the CB1 endocannabinoid receptors and shown to be susceptible to stress. METHODS/STUDY POPULATION: This study explored behavioral and neural impacts of early life stress in Long-Evans rats reared with or without limited access to bedding material during postnatal day (PND) 2-9. Corticosterone (CORT) levels were measured at PND8 and 70. During PND50-70, rats were assessed on Novel Object Recognition to test memory, Rotarod to evaluate cerebellar integrity, Elevated Plus Maze to assay anxiety, Social Preference, and Eyeblink Conditioning, a cerebellar-dependent and endocannabinoid-mediated task. Lipid analysis was performed on PND70 tissue samples of cerebellar interpositus (IP) nucleus via high-performance liquid chromatography and tandem mass spectrometry. RESULTS/ANTICIPATED RESULTS: Both male and female rats experiencing early life stress exhibited significantly impaired recognition memory (N = 16-20/group). Female rats having undergone stress exhibited decreased social preference compared to normally reared females (N = 11/group). Stressed males showed facilitated eyblink conditioning compared to normally reared males (N = 7-9/group). There were no group differences in rotarod or elevated plus maze performance or CORT levels at PND8 or 70 across rearing groups. At PND70, male rats experiencing early life stress exhibited a significant decrease in 2-arachidonoyl glycerol (2-AG) and arachidonic acid levels in the IP nucleus compared to normally reared males (N = 8-9/group). Compared to normally reared females, those experiencing early life stress exhibited a significant increase in prostaglandin E2 levels in the IP nucleus (N = 6-7/group). DISCUSSION/SIGNIFICANCE OF IMPACT: Early life stress, induced by limited bedding, resulted in sex-specific behavioral and lipid impairments. Results suggest that stress causes long-term alterations in endocannabinoid dynamics in males in the cerebellar IP nucleus and sex-related lipids in female cerebellum. These changes may contribute to observed long-term behavioral aberrations. Moreover, findings suggest these behavioral changes may be the result of negative-feedback dysfunction (as evidenced by decreased endocannabinoids in males) or increased neural inflammation or proliferation (as evidenced by increased prostaglandins in females). Future analysis will quantify mRNA and protein for cannabinoid receptors to better characterize aberrations to this system. Moreover, other neural regions dense with cannabinoid receptors (i.e., PFC, hippocampus) will be investigated. This work provides a basis for understanding stress impacts on the development of cognitive deficits observed in psychotic and anxiety disorders. Specifically, facilitation of eyblink conditioning complements research in humans with anxiety disorders. Broadly, understanding stress-related endocannabinoid dysregulation may provide insights into risks for, and the development of, psychopathology and uncover novel therapeutic targets with high translational power.
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spelling doaj.art-e56e1fce87a64e979e97029b6b4356c42023-03-09T12:30:28ZengCambridge University PressJournal of Clinical and Translational Science2059-86612019-03-01391010.1017/cts.2019.263004 Effects of Early Life Stress on Adult Behavioral and Neural Outcomes in RatsAlexandra Moussa-Tooks0Ken Mackie1John Green2Lisa Bartolomeo3Alex Gimeno4Eric Larson5Heather Bradshaw6Emma Leishman7Brian O’Donnell8William Hetrick9Indiana University School of MedicineDepartment of Psychology, University of VermontPsychological and Brain Sciences, Indiana UniversityPsychological and Brain Sciences, Indiana UniversityPsychological and Brain Sciences, Indiana UniversityPsychological and Brain Sciences, Indiana UniversityPsychological and Brain Sciences, Indiana UniversityPsychological and Brain Sciences, Indiana UniversityPsychological and Brain Sciences, Indiana UniversityPsychological and Brain Sciences, Indiana UniversityOBJECTIVES/SPECIFIC AIMS: Early life stress is known to greatly impact neurodevelopment during critical periods, conferring risk for various psychopathologies, including the onset and exacerbation of schizophrenia and anxiety disorders. The endocannabinoid system is highly integrated into the stress response and may be one means by which early life stress produces such deleterious effects. Using a naturalistic, ecologically valid animal model, this study explored interactions between the stress response and endocannabinoid systems within the cerebellum, a region dense with the CB1 endocannabinoid receptors and shown to be susceptible to stress. METHODS/STUDY POPULATION: This study explored behavioral and neural impacts of early life stress in Long-Evans rats reared with or without limited access to bedding material during postnatal day (PND) 2-9. Corticosterone (CORT) levels were measured at PND8 and 70. During PND50-70, rats were assessed on Novel Object Recognition to test memory, Rotarod to evaluate cerebellar integrity, Elevated Plus Maze to assay anxiety, Social Preference, and Eyeblink Conditioning, a cerebellar-dependent and endocannabinoid-mediated task. Lipid analysis was performed on PND70 tissue samples of cerebellar interpositus (IP) nucleus via high-performance liquid chromatography and tandem mass spectrometry. RESULTS/ANTICIPATED RESULTS: Both male and female rats experiencing early life stress exhibited significantly impaired recognition memory (N = 16-20/group). Female rats having undergone stress exhibited decreased social preference compared to normally reared females (N = 11/group). Stressed males showed facilitated eyblink conditioning compared to normally reared males (N = 7-9/group). There were no group differences in rotarod or elevated plus maze performance or CORT levels at PND8 or 70 across rearing groups. At PND70, male rats experiencing early life stress exhibited a significant decrease in 2-arachidonoyl glycerol (2-AG) and arachidonic acid levels in the IP nucleus compared to normally reared males (N = 8-9/group). Compared to normally reared females, those experiencing early life stress exhibited a significant increase in prostaglandin E2 levels in the IP nucleus (N = 6-7/group). DISCUSSION/SIGNIFICANCE OF IMPACT: Early life stress, induced by limited bedding, resulted in sex-specific behavioral and lipid impairments. Results suggest that stress causes long-term alterations in endocannabinoid dynamics in males in the cerebellar IP nucleus and sex-related lipids in female cerebellum. These changes may contribute to observed long-term behavioral aberrations. Moreover, findings suggest these behavioral changes may be the result of negative-feedback dysfunction (as evidenced by decreased endocannabinoids in males) or increased neural inflammation or proliferation (as evidenced by increased prostaglandins in females). Future analysis will quantify mRNA and protein for cannabinoid receptors to better characterize aberrations to this system. Moreover, other neural regions dense with cannabinoid receptors (i.e., PFC, hippocampus) will be investigated. This work provides a basis for understanding stress impacts on the development of cognitive deficits observed in psychotic and anxiety disorders. Specifically, facilitation of eyblink conditioning complements research in humans with anxiety disorders. Broadly, understanding stress-related endocannabinoid dysregulation may provide insights into risks for, and the development of, psychopathology and uncover novel therapeutic targets with high translational power.https://www.cambridge.org/core/product/identifier/S2059866119000268/type/journal_article
spellingShingle Alexandra Moussa-Tooks
Ken Mackie
John Green
Lisa Bartolomeo
Alex Gimeno
Eric Larson
Heather Bradshaw
Emma Leishman
Brian O’Donnell
William Hetrick
3004 Effects of Early Life Stress on Adult Behavioral and Neural Outcomes in Rats
Journal of Clinical and Translational Science
title 3004 Effects of Early Life Stress on Adult Behavioral and Neural Outcomes in Rats
title_full 3004 Effects of Early Life Stress on Adult Behavioral and Neural Outcomes in Rats
title_fullStr 3004 Effects of Early Life Stress on Adult Behavioral and Neural Outcomes in Rats
title_full_unstemmed 3004 Effects of Early Life Stress on Adult Behavioral and Neural Outcomes in Rats
title_short 3004 Effects of Early Life Stress on Adult Behavioral and Neural Outcomes in Rats
title_sort 3004 effects of early life stress on adult behavioral and neural outcomes in rats
url https://www.cambridge.org/core/product/identifier/S2059866119000268/type/journal_article
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