Lasting Impact of Chronic Adolescent Stress and Glucocorticoid Receptor Selective Modulation in Male and Female Rats

•Adolescent stress shapes adult behavior, physiology and neuronal activation to stress.•Effects are different within each sex.•Males had heightened emotional reactivity and reduction of neuronal excitation to stress.•Females developed a passive coping strategy and enhanced HPA axis stress reactivity...

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Veröffentlicht in:Psychoneuroendocrinology 2020-02, Vol.112, p.104490-104490, Article 104490
Hauptverfasser: Cotella, Evelin M., Morano, Rachel L., Wulsin, Aynara C., Martelle, Susan M., Lemen, Paige, Fitzgerald, Maureen, Packard, Benjamin A., Moloney, Rachel D., Herman, James P.
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container_title Psychoneuroendocrinology
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creator Cotella, Evelin M.
Morano, Rachel L.
Wulsin, Aynara C.
Martelle, Susan M.
Lemen, Paige
Fitzgerald, Maureen
Packard, Benjamin A.
Moloney, Rachel D.
Herman, James P.
description •Adolescent stress shapes adult behavior, physiology and neuronal activation to stress.•Effects are different within each sex.•Males had heightened emotional reactivity and reduction of neuronal excitation to stress.•Females developed a passive coping strategy and enhanced HPA axis stress reactivity.•The glucocorticoid receptor modulator CORT108297 only prevented some of these effects. Adolescent animals are vulnerable to the effects of stress on brain development. We hypothesized that long-term effects of adolescent chronic stress are mediated by glucocorticoid receptor (GR) signaling. We used a specific GR modulator (CORT108297) to pharmacologically disrupt GR signaling in adolescent rats during exposure to chronic variable stress (CVS). Male and female rats received 30 mg/kg of drug during a 2-week CVS protocol starting at PND46. Emotional reactivity (open field) and coping behaviors (forced swim test (FST)) were then tested in adulthood, 5 weeks after the end of the CVS protocol. Blood samples were collected two days before FST and serial samples after the onset of the swim test to determine baseline and stress response levels of HPA hormones respectively. Our results support differential behavioral, physiological and stress circuit reactivity to adolescent chronic stress exposure in males and females, with variable involvement of GR signaling. In response to adolescent stress, males had heightened reactivity to novelty and exhibited marked reduction in neuronal excitation following swim stress in adulthood, whereas females developed a passive coping strategy in the FST and enhanced HPA axis stress reactivity. Only the latter effect was attenuated by treatment with the GR modulator C108297. In summary, our data suggest that adolescent stress differentially affects emotional behavior and circuit development in males and females, and that GR manipulation during stress can reverse at least some of these effects.
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Adolescent animals are vulnerable to the effects of stress on brain development. We hypothesized that long-term effects of adolescent chronic stress are mediated by glucocorticoid receptor (GR) signaling. We used a specific GR modulator (CORT108297) to pharmacologically disrupt GR signaling in adolescent rats during exposure to chronic variable stress (CVS). Male and female rats received 30 mg/kg of drug during a 2-week CVS protocol starting at PND46. Emotional reactivity (open field) and coping behaviors (forced swim test (FST)) were then tested in adulthood, 5 weeks after the end of the CVS protocol. Blood samples were collected two days before FST and serial samples after the onset of the swim test to determine baseline and stress response levels of HPA hormones respectively. Our results support differential behavioral, physiological and stress circuit reactivity to adolescent chronic stress exposure in males and females, with variable involvement of GR signaling. In response to adolescent stress, males had heightened reactivity to novelty and exhibited marked reduction in neuronal excitation following swim stress in adulthood, whereas females developed a passive coping strategy in the FST and enhanced HPA axis stress reactivity. Only the latter effect was attenuated by treatment with the GR modulator C108297. 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Adolescent animals are vulnerable to the effects of stress on brain development. We hypothesized that long-term effects of adolescent chronic stress are mediated by glucocorticoid receptor (GR) signaling. We used a specific GR modulator (CORT108297) to pharmacologically disrupt GR signaling in adolescent rats during exposure to chronic variable stress (CVS). Male and female rats received 30 mg/kg of drug during a 2-week CVS protocol starting at PND46. Emotional reactivity (open field) and coping behaviors (forced swim test (FST)) were then tested in adulthood, 5 weeks after the end of the CVS protocol. Blood samples were collected two days before FST and serial samples after the onset of the swim test to determine baseline and stress response levels of HPA hormones respectively. Our results support differential behavioral, physiological and stress circuit reactivity to adolescent chronic stress exposure in males and females, with variable involvement of GR signaling. 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subjects Adaptation, Psychological - drug effects
Adaptation, Psychological - physiology
Adolescence
Age Factors
Animals
Aza Compounds - administration & dosage
Aza Compounds - pharmacology
Behavior, Animal - drug effects
Behavior, Animal - physiology
Chronic stress
CORT108297
Endocrinology & Metabolism
Female
Glucocorticoid receptor
Heterocyclic Compounds, 4 or More Rings - administration & dosage
Heterocyclic Compounds, 4 or More Rings - pharmacology
HPA axis
Hypothalamo-Hypophyseal System - metabolism
Hypothalamo-Hypophyseal System - physiopathology
Life Sciences & Biomedicine
Male
Neurosciences
Neurosciences & Neurology
Psychiatry
Rats
Rats, Sprague-Dawley
Receptors, Glucocorticoid - drug effects
Receptors, Glucocorticoid - physiology
Science & Technology
Sex Factors
Signal Transduction - drug effects
Signal Transduction - physiology
Stress, Psychological - metabolism
Stress, Psychological - physiopathology
title Lasting Impact of Chronic Adolescent Stress and Glucocorticoid Receptor Selective Modulation in Male and Female Rats
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