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Review
. 2021 Mar 10:3:649024.
doi: 10.3389/ftox.2021.649024. eCollection 2021.

Immune and Nervous Systems Interaction in Endocrine Disruptors Toxicity: The Case of Atrazine

Affiliations
Review

Immune and Nervous Systems Interaction in Endocrine Disruptors Toxicity: The Case of Atrazine

Valentina Galbiati et al. Front Toxicol. .

Abstract

Endocrine disruptors (ED) are natural and anthropogenic chemicals that can interfere with hormonal systems at different levels. As such, ED-induced alterations in hormone functions have been implicated in many diseases and pathological conditions, including adverse developmental, reproductive, neurological, cardiovascular, and immunological effects in mammals. The fact that ED may compete with several endogenous hormones for multiple receptors and pathways is not always fully considered. This results in a complex response that depends on the cellular context in terms of receptors and interacting proteins and, thus, may differ between tissues and circumstances. Microglia, neurons, and other immune cells are potential targets and still underappreciated actors in endocrine disruption. Due to the large scale of this topic, this review is not intended to provide a comprehensive review nor a systematic review of chemicals identified as endocrine disruptors. It focuses on the immune-neuro-endocrine network in ED toxicity and research gaps, using atrazine as an example to highlight this complexity and the interrelationship between the immune, endocrine, and nervous systems, and ED.

Keywords: atrazine; hormonally active compounds; immunotoxicity; neurotoxicity; steroid hormones.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Graphical representation of atrazine neuro-endocrine and immune interaction.

References

    1. Agopian A. J., Lupo P. J., Canfield M. A., Langlois P. H. (2013). Case-control study of maternal residential atrazine exposure and male genital malformations. Am. J. Med. Genet. A 161A, 977–982. 10.1002/ajmg.a.35815 - DOI - PubMed
    1. Almberg K. S., Turyk M. E., Jones R. M., Rankin K., Freels S., Stayner L. T. (2018). Atrazine contamination of drinking water and adverse birth outcomes in community water systems with elevated atrazine in Ohio, 2006-2008. Int. J. Environ. Res. Public Health 15:1889. 10.3390/ijerph15091889 - DOI - PMC - PubMed
    1. Alvarez-Bolado G. (2019). Development of neuroendocrine neurons in the mammalian hypothalamus. Cell Tissue Res. 375, 23–39. 10.1007/s00441-018-2859-1 - DOI - PubMed
    1. Atwood D., Paisley-Jones C. (2017). Pesticides Industry Sales and Usage 2008-2012 Estimates. Washington, DC: United States Environmental Protection Agency.
    1. Bansal A., Henao-Mejia J., Simmons R. A. (2018). Immune system: an emerging player in mediating effects of endocrine disruptors on metabolic health. Endocrinology 159, 32–45. 10.1210/en.2017-00882 - DOI - PMC - PubMed