Prenatal stress may increase vulnerability to life events: comparison with the effects of prenatal dexamethasone

Research output: Contribution to journalJournal articleResearchpeer-review

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Prenatal stress may increase vulnerability to life events : comparison with the effects of prenatal dexamethasone. / Hougaard, Karin S; Andersen, Maibritt B; Kjaer, Sanna L; Hansen, Åse Marie; Werge, Thomas; Lund, Søren P.

In: Brain Research, Vol. 159, No. 1, 08.09.2005, p. 55-63.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Hougaard, KS, Andersen, MB, Kjaer, SL, Hansen, ÅM, Werge, T & Lund, SP 2005, 'Prenatal stress may increase vulnerability to life events: comparison with the effects of prenatal dexamethasone', Brain Research, vol. 159, no. 1, pp. 55-63. https://doi.org/10.1016/j.devbrainres.2005.06.014

APA

Hougaard, K. S., Andersen, M. B., Kjaer, S. L., Hansen, Å. M., Werge, T., & Lund, S. P. (2005). Prenatal stress may increase vulnerability to life events: comparison with the effects of prenatal dexamethasone. Brain Research, 159(1), 55-63. https://doi.org/10.1016/j.devbrainres.2005.06.014

Vancouver

Hougaard KS, Andersen MB, Kjaer SL, Hansen ÅM, Werge T, Lund SP. Prenatal stress may increase vulnerability to life events: comparison with the effects of prenatal dexamethasone. Brain Research. 2005 Sep 8;159(1):55-63. https://doi.org/10.1016/j.devbrainres.2005.06.014

Author

Hougaard, Karin S ; Andersen, Maibritt B ; Kjaer, Sanna L ; Hansen, Åse Marie ; Werge, Thomas ; Lund, Søren P. / Prenatal stress may increase vulnerability to life events : comparison with the effects of prenatal dexamethasone. In: Brain Research. 2005 ; Vol. 159, No. 1. pp. 55-63.

Bibtex

@article{123a28d5d336491cbd9325b258b3a3ee,
title = "Prenatal stress may increase vulnerability to life events: comparison with the effects of prenatal dexamethasone",
abstract = "Prenatal stress has been associated with a variety of alterations in the offspring. The presented observations suggest that rather than causing changes in the offspring per se, prenatal stress may increase the organism's vulnerability to aversive life events. Offspring of rat dams stressed gestationally by chronic mild stress (CMS, a variable schedule of different stressors) or dexamethasone (DEX, a synthetic glucocorticoid, i.e., a pharmacological stressor) was tested for reactivity by testing their acoustic startle response (ASR). Two subsets of offspring were tested. One was experimentally na{\"i}ve at the time of ASR testing, whereas the other had been through blood sampling for assessment of the hormonal stress response to restraint, 3 months previously. Both prenatal CMS and dexamethasone increased ASR in the offspring compared to controls, but only in prenatally stressed offspring that had been blood sampled 3 months previously. In conclusion, similarity of the effects of maternal gestational exposure to a regular stress schedule and of exposure to a synthetic glucocorticoid suggests that maternal glucocorticoids may be a determining factor for changes in the regulatory mechanisms of the acoustic startle response. Further, a single aversive life event showed capable of changing the reactivity of prenatally stressed offspring, whereas offspring of dams going through a less stressful gestation was largely unaffected by this event. This suggests that circumstances dating back to the very beginning of life affect the individual's sensitivity towards experiences in life after birth. The prenatal environment may thus form part of the explanation of the considerable individual variation in the development of psychopathology.",
keywords = "Acoustic Stimulation, Animals, Animals, Newborn, Anxiety Disorders, Brain, Dexamethasone, Fear, Female, Glucocorticoids, Hormones, Hypothalamo-Hypophyseal System, Life Change Events, Mental Disorders, Pituitary-Adrenal System, Pregnancy, Prenatal Exposure Delayed Effects, Rats, Rats, Wistar, Reflex, Startle, Stress, Psychological, Comparative Study, Journal Article",
author = "Hougaard, {Karin S} and Andersen, {Maibritt B} and Kjaer, {Sanna L} and Hansen, {{\AA}se Marie} and Thomas Werge and Lund, {S{\o}ren P}",
year = "2005",
month = sep,
day = "8",
doi = "10.1016/j.devbrainres.2005.06.014",
language = "English",
volume = "159",
pages = "55--63",
journal = "Brain Research",
issn = "0006-8993",
publisher = "Elsevier",
number = "1",

}

RIS

TY - JOUR

T1 - Prenatal stress may increase vulnerability to life events

T2 - comparison with the effects of prenatal dexamethasone

AU - Hougaard, Karin S

AU - Andersen, Maibritt B

AU - Kjaer, Sanna L

AU - Hansen, Åse Marie

AU - Werge, Thomas

AU - Lund, Søren P

PY - 2005/9/8

Y1 - 2005/9/8

N2 - Prenatal stress has been associated with a variety of alterations in the offspring. The presented observations suggest that rather than causing changes in the offspring per se, prenatal stress may increase the organism's vulnerability to aversive life events. Offspring of rat dams stressed gestationally by chronic mild stress (CMS, a variable schedule of different stressors) or dexamethasone (DEX, a synthetic glucocorticoid, i.e., a pharmacological stressor) was tested for reactivity by testing their acoustic startle response (ASR). Two subsets of offspring were tested. One was experimentally naïve at the time of ASR testing, whereas the other had been through blood sampling for assessment of the hormonal stress response to restraint, 3 months previously. Both prenatal CMS and dexamethasone increased ASR in the offspring compared to controls, but only in prenatally stressed offspring that had been blood sampled 3 months previously. In conclusion, similarity of the effects of maternal gestational exposure to a regular stress schedule and of exposure to a synthetic glucocorticoid suggests that maternal glucocorticoids may be a determining factor for changes in the regulatory mechanisms of the acoustic startle response. Further, a single aversive life event showed capable of changing the reactivity of prenatally stressed offspring, whereas offspring of dams going through a less stressful gestation was largely unaffected by this event. This suggests that circumstances dating back to the very beginning of life affect the individual's sensitivity towards experiences in life after birth. The prenatal environment may thus form part of the explanation of the considerable individual variation in the development of psychopathology.

AB - Prenatal stress has been associated with a variety of alterations in the offspring. The presented observations suggest that rather than causing changes in the offspring per se, prenatal stress may increase the organism's vulnerability to aversive life events. Offspring of rat dams stressed gestationally by chronic mild stress (CMS, a variable schedule of different stressors) or dexamethasone (DEX, a synthetic glucocorticoid, i.e., a pharmacological stressor) was tested for reactivity by testing their acoustic startle response (ASR). Two subsets of offspring were tested. One was experimentally naïve at the time of ASR testing, whereas the other had been through blood sampling for assessment of the hormonal stress response to restraint, 3 months previously. Both prenatal CMS and dexamethasone increased ASR in the offspring compared to controls, but only in prenatally stressed offspring that had been blood sampled 3 months previously. In conclusion, similarity of the effects of maternal gestational exposure to a regular stress schedule and of exposure to a synthetic glucocorticoid suggests that maternal glucocorticoids may be a determining factor for changes in the regulatory mechanisms of the acoustic startle response. Further, a single aversive life event showed capable of changing the reactivity of prenatally stressed offspring, whereas offspring of dams going through a less stressful gestation was largely unaffected by this event. This suggests that circumstances dating back to the very beginning of life affect the individual's sensitivity towards experiences in life after birth. The prenatal environment may thus form part of the explanation of the considerable individual variation in the development of psychopathology.

KW - Acoustic Stimulation

KW - Animals

KW - Animals, Newborn

KW - Anxiety Disorders

KW - Brain

KW - Dexamethasone

KW - Fear

KW - Female

KW - Glucocorticoids

KW - Hormones

KW - Hypothalamo-Hypophyseal System

KW - Life Change Events

KW - Mental Disorders

KW - Pituitary-Adrenal System

KW - Pregnancy

KW - Prenatal Exposure Delayed Effects

KW - Rats

KW - Rats, Wistar

KW - Reflex, Startle

KW - Stress, Psychological

KW - Comparative Study

KW - Journal Article

U2 - 10.1016/j.devbrainres.2005.06.014

DO - 10.1016/j.devbrainres.2005.06.014

M3 - Journal article

C2 - 16085319

VL - 159

SP - 55

EP - 63

JO - Brain Research

JF - Brain Research

SN - 0006-8993

IS - 1

ER -

ID: 173709700