Abstract

Although pregnant women are advised to consume methyl-donor food, some reports suggest an adverse outcome. We investigated whether maternal melatonin therapy can prevent hypertension induced by a high methyl-donor diet. Female Sprague-Dawley rats received either a normal diet, a methyl-deficient diet (L-MD), or a high methyl-donor diet (H-MD) during gestation and lactation. Male offspring were assigned to four groups (n = 7–8/group): control, L-MD, H-MD, and H-MD rats were given melatonin (100 mg/L) with their drinking water throughout the period of pregnancy and lactation (H-MD+M). At 12 weeks of age, male offspring exposed to a L-MD or a H-MD diet developed programmed hypertension. Maternal melatonin therapy attenuated high methyl-donor diet-induced programmed hypertension. A maternal L-MD diet and H-MD diet caused respectively 938 and 806 renal transcripts to be modified in adult offspring. The protective effects of melatonin against programmed hypertension relate to reduced oxidative stress, increased urinary NO2− level, and reduced renal expression of sodium transporters. A H-MD or L-MD diet may upset the balance of methylation status, leading to alterations of renal transcriptome and programmed hypertension. A better understanding of reprogramming effects of melatonin might aid in developing a therapeutic strategy for the prevention of hypertension in adult offspring exposed to an excessive maternal methyl-supplemented diet.

Highlights

  • Hypertension remains a leading threat to human health

  • Pregnant rats were randomly divided into four groups: controls, rats treated with a methyl-deficient diet (L-MD), rats treated with a high methyl-donor diet (H-MD), and rats treated with a high methyl-donor diet plus melatonin (H-MD+M) during the whole pregnancy and lactation period

  • In line with earlier reports demonstrating the beneficial effects of maternal melatonin therapy study in a number of models of developmental programming [19], we found that maternal melatonin therapy alleviates high methyl-donor diet-induced programmed hypertension

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Summary

Introduction

Hypertension remains a leading threat to human health. An estimated one in three adults worldwide have high blood pressure (BP). Adulthood hypertension can originate in early life. Maternal nutrition plays a critical role in fetal growth and development. Suboptimal nutrition in fetal and infantile life induces morphological changes and functional adaption, increasing the risk for developing chronic diseases in adulthood by so-called nutritional programming [1]. This concept is formerly known as the developmental origins of adult health and disease (DOHaD) [2]

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