Prenatal maternal stress alters depression-related symptoms in a strain - and sex-dependent manner in rodent offspring

Stress during pregnancy adversely affects foetal development and leads to later behavioural outcomes in offspring. Preclinical studies have reported conflicting effects of prenatal stress on depression-related symptoms in rodent offspring. This study aimed to study the combined effect of strain and...

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Veröffentlicht in:Life sciences (1973) 2020-06, Vol.251, p.117597-12, Article 117597
Hauptverfasser: Enayati, Mohsen, Mosaferi, Belal, Homberg, Judith R., Diniz, Danielle Mendes, Salari, Ali-Akbar
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container_end_page 12
container_issue
container_start_page 117597
container_title Life sciences (1973)
container_volume 251
creator Enayati, Mohsen
Mosaferi, Belal
Homberg, Judith R.
Diniz, Danielle Mendes
Salari, Ali-Akbar
description Stress during pregnancy adversely affects foetal development and leads to later behavioural outcomes in offspring. Preclinical studies have reported conflicting effects of prenatal stress on depression-related symptoms in rodent offspring. This study aimed to study the combined effect of strain and sex on prenatal stress outcomes in a single study. To this end, male and female offspring from outbred Wistar and inbred Lewis rats, and outbred NMRI and inbred C57BL6 mice were compared. As outcomes we focussed on depression-related behaviour and related molecular and neurochemical parameters. Prenatally stressed and non-stressed offspring were subjected to the sucrose preference, novelty-suppressed feeding, tail suspension, and forced swim tests. We measured basal and stress-induced corticosterone levels in the serum, and brain-derived-neurotrophic-factor (BDNF), interleukin-1β, tumor necrosis factor-α, glutamate and serotonin in the brain to determine changes in hypothalamic–pituitary–adrenal-(HPA)-axis function, neuroplasticity, neuroinflammation, and neurotransmission. Our findings revealed that prenatal stress increases depression-like behaviour, HPA-axis (re) activity, pro-inflammatory cytokines and glutamate levels, and decreases BDNF and serotonin levels in a strain and sex-dependent manner in rodent offspring. Overall, male and female Lewis rats, female Wistar rats, male NMRI mice and female C57BL6 mice were found to be most responsive to prenatal stress. Based on these results, we conclude that genetic background and sex contribute to the great diversity in the effects of prenatal maternal stress in rodents. •Maternal stress increased depression-like behavior in offspring in adulthood.•Maternal stress enhanced basal and stress-induced corticosterone levels in offspring.•Maternal stress decreased BDNF and increased IL-1β and TNF-α levels in the brain of offspring.•Maternal stress decreased serotonin and increased glutamate levels in the brain of offspring.•Maternal stress affects Behavior and biochemistry in a strain and sex dependent manner.
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Our findings revealed that prenatal stress increases depression-like behaviour, HPA-axis (re) activity, pro-inflammatory cytokines and glutamate levels, and decreases BDNF and serotonin levels in a strain and sex-dependent manner in rodent offspring. Overall, male and female Lewis rats, female Wistar rats, male NMRI mice and female C57BL6 mice were found to be most responsive to prenatal stress. 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subjects Animals
Brain
Brain - metabolism
Brain tumors
Brain-derived neurotrophic factor
Corticosterone
Corticosterone - blood
Cytokines
Depression
Depression - psychology
Female
Females
Glutamate
HPA-axis
Hypothalamic-pituitary-adrenal axis
Hypothalamus
IL-1β
Inbreeding
Inflammation
Interleukins
Male
Mental depression
Mice
Mice, Inbred C57BL
Neuroplasticity
Neurotransmission
Offspring
Pituitary
Pregnancy
Pregnancy Complications - psychology
Prenatal experience
Prenatal Exposure Delayed Effects - psychology
Rats
Rats, Inbred Lew
Rats, Wistar
Rodents
Serotonin
Sex
Sex Factors
Species Specificity
Strain
Stress
Stress, Psychological - psychology
Sucrose
Sugar
Tumor necrosis factor-α
title Prenatal maternal stress alters depression-related symptoms in a strain - and sex-dependent manner in rodent offspring
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