Abstract

Previous studies have demonstrated that endocrine disruptors (EDs) can promote the transgenerational inheritance of disease susceptibility. Among the many existing EDs, 2,3,7,8-tetrachlordibenzo-p-dioxin (TCDD) affects reproductive health, including in humans, following direct occupational exposure or environmental disasters, for instance the Agent Orange sprayed during the Vietnam War. Conversely, few studies have focused on TCDD multigenerational and transgenerational effects on human reproductive health, despite the high amount of evidence in animal models of such effects on male and female reproductive health that mimic human reproductive system disorders. Importantly, these studies show that paternal ancestral TCDD exposure substantially contributes to pregnancy outcome and fetal health, although pregnancy outcome is considered tightly related to the woman’s health. In this work, we conducted a systematic review of the literature and a knowledge synthesis in order (i) to describe the findings obtained in rodent models concerning TCDD transgenerational effects on reproductive health and (ii) to discuss the epigenetic molecular alterations that might be involved in this process. As ancestral toxicant exposure cannot be changed in humans, identifying the crucial reproductive functions that are negatively affected by such exposure may help clinicians to preserve male and female fertility and to avoid adverse pregnancy outcomes.

Highlights

  • It has been determined that some adult diseases are initiated during fetal and neonatal development

  • The question of whether endocrine disruptors (EDs) fetal exposure results in heritable epigenetic alterations that might negatively affect the reproductive function of future generations remains a key issue for researchers and clinicians

  • This systematic review highlighted the occurrence of transgenerational effects, such as subfertility and adverse pregnancy outcomes, that might implicate TCDD-mediated epigenetic modifications in both germlines

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Summary

Introduction

It has been determined that some adult diseases are initiated during fetal and neonatal development. A considerable and growing body of evidence indicates that chemicals and environmental toxicants might favor a transgenerational phenotype, which has important health consequences [4,5,6,7,8]. This underlying biological mechanism is called transgenerational epigenetic inheritance, a form of non-genetic inheritance that involves the transmission of an altered epigenome and its phenotypes through the germline across generations in the absence of the direct environmental exposure that caused the alteration [6,9,10]. The most studied epigenetic mechanisms involved in transgenerational inheritance are DNA methylation, histone modifications, methylation profile changes, and non-coding RNAs, including microRNA, chromatin structure, and RNA methylation [11]

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