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Maternal obesity and the developmental programming of hypertension: a role for leptin
P D Taylor1, A-M Samuelsson, L Poston
1Division of Women's Health, Women's Health Academic Centre, King's College London and King's Health Partners, London, UK.
Insights
Maternal obesity during pregnancy may permanently alter offspring
Area of Science:
- Developmental biology
- Cardiovascular science
- Endocrinology
Background:
- Maternal pre-pregnancy body mass index (BMI) and gestational weight gain are linked to offspring cardio-metabolic risks.
- Animal models suggest maternal obesity impacts offspring cardiovascular function and blood pressure regulation.
- Leptin, involved in appetite and sympathetic pathways, is implicated in obesity-related hypertension.
Purpose of the Study:
- To explore the role of leptin in developmental programming of hypertension in offspring of obese mothers.
- To review evidence linking maternal obesity, neonatal leptin exposure, and offspring hypertension.
Main Methods:
- Review of mother-child cohort studies.
- Analysis of animal models (sheep, non-human primates, rodents).
- Examination of rodent studies on neonatal hyperleptinemia and hypothalamic development.
Main Results:
- Maternal obesity may permanently alter central blood pressure regulatory pathways in offspring.
- Neonatal hyperleptinemia in rodents leads to heightened sympathetic tone and adult hypertension.
- Altered neonatal leptin profiles are associated with lasting hypothalamic changes.
Conclusions:
- Early-life leptin exposure, influenced by maternal obesity, may program offspring for essential hypertension.
- Further research in human mother-child cohorts is crucial to confirm these associations.
- Leptin's role in developmental programming of hypertension warrants attention in obese pregnancies.
Abstract:
Mother-child cohort studies have established that both pre-pregnancy body mass index (BMI) and gestational weight gain are independently associated with cardio-metabolic risk factors in young adult offspring, including systolic and diastolic blood pressure. Animal models in sheep and non-human primates provide further evidence for the influence of maternal obesity on offspring cardiovascular function, whilst recent studies in rodents suggest that perinatal exposure to the metabolic milieu of maternal obesity may permanently change the central regulatory pathways involved in blood pressure regulation. Leptin plays an important role in the central control of appetite, is also involved in activation of efferent sympathetic pathways to both thermogenic and non-thermogenic tissues, such as the kidney, and is therefore implicated in obesity-related hypertension. Leptin is also thought to have a neurotrophic role in the development of the hypothalamus, and altered neonatal leptin profiles secondary to maternal obesity are associated with permanently altered hypothalamic structure and function. In rodent studies, maternal obesity confers persistent sympathoexcitatory hyper-responsiveness and hypertension acquired in the early stages of development. Experimental neonatal hyperleptinaemia in naive rat pups provides further evidence of heightened sympathetic tone and proof of principle that hyperleptinaemia during a critical window of hypothalamic development may directly lead to adulthood hypertension. Insight from these animal models raises the possibility that early-life exposure to leptin in humans may lead to early onset essential hypertension. Ongoing mother-child cohort and intervention studies in obese pregnant women provide a unique opportunity to address associations between maternal obesity and offspring cardiovascular function. The goal of the review is to highlight the potential importance of leptin in the developmental programming of hypertension in obese pregnancy.
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