Early life stress leads to developmental and sex selective effects on performance in a novel object placement task

Disruptions in early life care, including neglect, extreme poverty, and trauma, influence neural development and increase the risk for and severity of pathology. Significant sex disparities have been identified for affective pathology, with females having an increased risk of developing anxiety and...

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Main Authors: Kevin G. Bath, PhD, Arielle Schilit Nitenson, Ezra Lichtman, Chelsea Lopez, Whitney Chen, Meghan Gallo, Haley Goodwill, Gabriela Manzano-Nieves
Format: Article
Language:English
Published: Elsevier 2017-12-01
Series:Neurobiology of Stress
Online Access:http://www.sciencedirect.com/science/article/pii/S2352289516300534
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spelling doaj-a17443005b2c4a11bc26ec6f9d4162ce2020-11-24T20:57:08ZengElsevierNeurobiology of Stress2352-28952017-12-0175767Early life stress leads to developmental and sex selective effects on performance in a novel object placement taskKevin G. Bath, PhD0Arielle Schilit Nitenson1Ezra Lichtman2Chelsea Lopez3Whitney Chen4Meghan Gallo5Haley Goodwill6Gabriela Manzano-Nieves7Department of Cognitive, Linguistic, and Psychological Sciences, Brown University, Providence RI 02912, United States; Corresponding author. Department of Cognitive, Linguistic, and Psychological Sciences, Box 1821 Brown University, Providence, RI 02912, United States.Department of Neuroscience, Brown University, Providence, RI 02912, United StatesYale School of Medicine, New Haven, CT 06510, United StatesDepartment of Cognitive, Linguistic, and Psychological Sciences, Brown University, Providence RI 02912, United StatesDepartment of Neuroscience, University of California at San Francisco, San Francisco, CA 94158, United StatesDepartment of Cognitive, Linguistic, and Psychological Sciences, Brown University, Providence RI 02912, United StatesDepartment of Neuroscience, Brown University, Providence, RI 02912, United StatesDepartment of Neuroscience, Brown University, Providence, RI 02912, United StatesDisruptions in early life care, including neglect, extreme poverty, and trauma, influence neural development and increase the risk for and severity of pathology. Significant sex disparities have been identified for affective pathology, with females having an increased risk of developing anxiety and depressive disorder. However, the effects of early life stress (ELS) on cognitive development have not been as well characterized, especially in reference to sex specific impacts of ELS on cognitive abilities over development. In mice, fragmented maternal care resulting from maternal bedding restriction, was used to induce ELS. The development of spatial abilities were tracked using a novel object placement (NOP) task at several different ages across early development (P21, P28, P38, P50, and P75). Male mice exposed to ELS showed significant impairments in the NOP task compared with control reared mice at all ages tested. In female mice, ELS led to impaired NOP performance immediately following weaning (P21) and during peri-adolescence (P38), but these effects did not persist into early adulthood. Prior work has implicated impaired hippocampus neurogenesis as a possible mediator of negative outcomes in ELS males. In the hippocampus of behaviorally naïve animals there was a significant decrease in expression of Ki-67 (proliferative marker) and doublecortin (DCX-immature cell marker) as mice aged, and a more rapid developmental decline in these markers in ELS reared mice. However, the effect of ELS dissipated by P28 and no main effect of sex were observed. Together these results indicate that ELS impacts the development of spatial abilities in both male and female mice and that these effects are more profound and lasting in males.http://www.sciencedirect.com/science/article/pii/S2352289516300534
collection DOAJ
language English
format Article
sources DOAJ
author Kevin G. Bath, PhD
Arielle Schilit Nitenson
Ezra Lichtman
Chelsea Lopez
Whitney Chen
Meghan Gallo
Haley Goodwill
Gabriela Manzano-Nieves
spellingShingle Kevin G. Bath, PhD
Arielle Schilit Nitenson
Ezra Lichtman
Chelsea Lopez
Whitney Chen
Meghan Gallo
Haley Goodwill
Gabriela Manzano-Nieves
Early life stress leads to developmental and sex selective effects on performance in a novel object placement task
Neurobiology of Stress
author_facet Kevin G. Bath, PhD
Arielle Schilit Nitenson
Ezra Lichtman
Chelsea Lopez
Whitney Chen
Meghan Gallo
Haley Goodwill
Gabriela Manzano-Nieves
author_sort Kevin G. Bath, PhD
title Early life stress leads to developmental and sex selective effects on performance in a novel object placement task
title_short Early life stress leads to developmental and sex selective effects on performance in a novel object placement task
title_full Early life stress leads to developmental and sex selective effects on performance in a novel object placement task
title_fullStr Early life stress leads to developmental and sex selective effects on performance in a novel object placement task
title_full_unstemmed Early life stress leads to developmental and sex selective effects on performance in a novel object placement task
title_sort early life stress leads to developmental and sex selective effects on performance in a novel object placement task
publisher Elsevier
series Neurobiology of Stress
issn 2352-2895
publishDate 2017-12-01
description Disruptions in early life care, including neglect, extreme poverty, and trauma, influence neural development and increase the risk for and severity of pathology. Significant sex disparities have been identified for affective pathology, with females having an increased risk of developing anxiety and depressive disorder. However, the effects of early life stress (ELS) on cognitive development have not been as well characterized, especially in reference to sex specific impacts of ELS on cognitive abilities over development. In mice, fragmented maternal care resulting from maternal bedding restriction, was used to induce ELS. The development of spatial abilities were tracked using a novel object placement (NOP) task at several different ages across early development (P21, P28, P38, P50, and P75). Male mice exposed to ELS showed significant impairments in the NOP task compared with control reared mice at all ages tested. In female mice, ELS led to impaired NOP performance immediately following weaning (P21) and during peri-adolescence (P38), but these effects did not persist into early adulthood. Prior work has implicated impaired hippocampus neurogenesis as a possible mediator of negative outcomes in ELS males. In the hippocampus of behaviorally naïve animals there was a significant decrease in expression of Ki-67 (proliferative marker) and doublecortin (DCX-immature cell marker) as mice aged, and a more rapid developmental decline in these markers in ELS reared mice. However, the effect of ELS dissipated by P28 and no main effect of sex were observed. Together these results indicate that ELS impacts the development of spatial abilities in both male and female mice and that these effects are more profound and lasting in males.
url http://www.sciencedirect.com/science/article/pii/S2352289516300534
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