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Effects of Endocrine-Disrupting Chemicals on Adrenal Function
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This review examines how endocrine-disrupting chemicals, including microplastics, affect the adrenal glands, which produce hormones that regulate metabolism, blood pressure, and stress response. Evidence shows these chemicals can damage adrenal gland structure and disrupt hormone production, with some effects even passing to future generations. The authors argue that adrenal glands have been overlooked in safety testing and need to be included in screening for harmful chemicals.
The adrenal glands play crucial roles in regulating metabolism, blood pressure, immune system function, and response to stress through the secretion of hormones. Despite their critical functions, the adrenal glands are often overlooked in studies on the effects of potential toxicants. Research across human, animal, and in vitro studies has identified more than 60 compounds that can induce adrenocortical toxicity. These compounds, known as endocrine-disrupting chemicals (EDCs), are natural or synthetic substances that interfere with the endocrine system. This review aims to provide an overview of the effects of 4 major families of EDCs-flame retardants, bisphenols, phthalates, and microplastics-on the function of the adrenal glands. The PubMed database was searched for studies reporting the effects of the chemicals in these 4 families on the adrenal glands. There is clear evidence that the morphology and function of the adrenal gland are affected, particularly through disrupting the steroidogenic pathway. Additionally, some EDCs have been shown to exert transgenerational effects, raising further concerns about their long-term effect. However, most EDCs have not been thoroughly evaluated for their effects on the function of the adrenal glands, especially in human studies. Thus, developing regulatory testing guideline to include the adrenal glands in the screening of EDCs is urgently needed.
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This study found that bisphenol A, F, and S all disrupt steroidogenesis in adrenocortical cells at non-cytotoxic concentrations in cell culture, producing compound-specific alterations in hormone levels, providing evidence that BPF and BPS are not necessarily safer endocrine alternatives to BPA.
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