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Updated: May 10, 2026

Using a Murine Model of Psychosocial Stress in Pregnancy as a Translationally Relevant Paradigm for Psychiatric Disorders in Mothers and Infants
Published on: June 13, 2021
Transmitting biological effects of stress in utero: implications for mother and offspring
Rebecca M Reynolds1, Javier Labad, Claudia Buss
1Endocrinology Unit, Centre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.
Insights
Adverse prenatal conditions and early life stress can program the fetus for later-life diseases, impacting even normal birth weight infants. Understanding these mechanisms is crucial for developing interventions to improve offspring health.
Area of Science:
- Developmental biology
- Reproductive medicine
- Public health
Background:
- Adverse in utero environments can permanently alter fetal development, increasing later-life disease risk.
- Low birth weight is a marker for intrauterine stress, linked to cardiometabolic and psychiatric diseases.
- These risks extend beyond low birth weight to infants within the normal range.
Purpose of the Study:
- To explore how early life stress, particularly prenatal stress, affects offspring health.
- To investigate the role of maternal and fetal hypothalamic-pituitary-adrenal (HPA) axes in mediating stress effects.
- To identify potential intervention points in the periconceptional, pregnancy, or postpartum periods.
Main Methods:
- Review of epidemiological studies linking birth weight and adult disease.
- Examination of animal models demonstrating HPA axis changes due to stress.
- Analysis of human data on stress, glucocorticoids, and fetal development.
- Consideration of maternal factors like obesity and socioeconomic status.
Main Results:
- Prenatal stress, mediated by glucocorticoids, can alter fetal development and increase disease susceptibility.
- Maternal obesity and socioeconomic deprivation exacerbate prenatal stress impacts.
- Early postnatal stress, like maltreatment, can compound prenatal effects.
- Mechanisms involve changes in glucocorticoid action or metabolism in the fetus.
Conclusions:
- Early life stress significantly impacts long-term offspring health through biological programming.
- Understanding transmission mechanisms from mother to fetus is key for early intervention strategies.
- Interventions targeting the periconceptional, prenatal, or early postnatal periods hold promise for mitigating risks.
Abstract:
The developing foetus makes adaptations to an adverse in utero environment which may lead to permanent changes in structure and physiology, thus 'programming' the foetus to risk of ill health in later life. Epidemiological studies have shown associations between low birth weight, a surrogate marker of an adverse intrauterine environment, and a range of diseases in adult life including cardiometabolic and psychiatric disease. These associations do not apply exclusively to low birth weight babies but also to newborns within the normal birth weight range. Early life stress, including stressors in the prenatal and early postnatal period, is a key factor that can have long-term effects on offspring health. Animal studies show this is mediated through changes in the maternal and foetal hypothalamic-pituitary-adrenal axes resulting in foetal exposure to excess glucocorticoids. Data in humans are more limited but support that the biological effects of stress in utero may be transmitted through changes in glucocorticoid action or metabolism. Common contemporary physical and social stressors of maternal obesity and socio-economic deprivation impact on the maternal response to pregnancy and the prevailing hormonal milieu that the developing foetus will be exposed to. Prenatal stress may also be compounded by early postnatal stresses such as childhood maltreatment with resultant adverse effects for the offspring. Understanding of the mechanisms whereby these stressors are transmitted from mother to foetus will not only improve our knowledge of normal foetal development but will also help identify novel pathways for early intervention either in the periconceptional, pregnancy or the early postpartum period.
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