Abstract

Maternal exposure to endocrine disrupting chemicals (EDCs) and a high-fat intake may induce the developmental programming of hypertension in adult offspring. Bisphenol A (BPA) is one of the most commonly environmental EDCs. As the nitric oxide (NO) and aryl hydrocarbon receptor (AHR) signaling pathways both contribute to the pathogenesis of hypertension, we evaluated whether resveratrol, an antioxidant and an AHR antagonist, can prevent hypertension programmed by a maternal BPA and HF diet. Sixteen-week-old male rat offspring were assigned to six groups (n = 8 per group): Control, HF (D12331, Research Diets), BPA (50 μg/kg/day), HF + BPA, BPA + R (resveratrol 50mg/L in drinking water throughout pregnancy and lactation), and HF + BPA + R. Maternal BPA exposure exacerbated hypertension programmed by HF consumption in adult male offspring, which was protected by maternal resveratrol therapy. The BPA and HF diet synergistically induced oxidative stress in offspring kidneys, which resveratrol treatment prevented. We observed that HF + BPA-induced programmed hypertension was associated with a decreased NO bioavailability, increased oxidative stress, and an activated AHR signaling pathway. The beneficial effects of resveratrol are relevant to restoring NO bioavailability, reducing oxidative stress, and antagonizing the AHR signaling pathway. Our results cast a new light on resveratrol as a reprogramming strategy to protect against hypertension programmed by combined BPA and HF exposure, but this strategy has yet to be translated into clinical applications.

Highlights

  • Maternal exposure to environmental chemicals, such as endocrine disrupting chemicals (EDCs), can increase disease risk later in life

  • At 16 weeks of age, both HF diet and bisphenol A (BPA) exposure resulted in the elevation of systolic blood pressure (SBP)

  • Maternal BPA exposure exacerbates hypertension programmed by HF intake in male adult offspring

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Summary

Introduction

Maternal exposure to environmental chemicals, such as endocrine disrupting chemicals (EDCs), can increase disease risk later in life. This concept is known as the developmental origins of health and disease (DOHaD) [1]. One of the most commonly environmental EDC exposures is bisphenol A (BPA). BPA has been reported to be associated with the development of cardiovascular disease and hypertension in both children and adults [2]. A previous study showed that exposure to BPA during pregnancy is associated with higher blood pressure (BP) of children [3]. The impacts of maternal BPA exposure on BP in adult offspring remain unclear

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