» Articles » PMID: 33042007

Bisphenols Threaten Male Reproductive Health Via Testicular Cells

Overview
Specialty Endocrinology
Date 2020 Oct 12
PMID 33042007
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Male reproductive function and health are largely dependent on the testes, which are strictly regulated by their major cell components, i. e., Sertoli, Leydig, and germ cells. Sertoli cells perform a crucial phagocytic function in addition to supporting the development of germ cells. Leydig cells produce hormones essential for male reproductive function, and germ cell quality is a key parameter for male fertility assessment. However, these cells have been identified as primary targets of endocrine disruptors, including bisphenols. Bisphenols are a category of man-made organic chemicals used to manufacture plastics, epoxy resins, and personal care products such as lipsticks, face makeup, and nail lacquers. Despite long-term uncertainty regarding their safety, bisphenols are still being used worldwide, especially bisphenol A. While considerable attention has been paid to the effects of bisphenols on health, current bisphenol-related reproductive health cases indicate that greater attention should be given to these chemicals. Bisphenols, especially bisphenol A, F, and S, have been reported to elicit various effects on testicular cells, including apoptosis, DNA damage, disruption of intercommunication among cells, mitochondrial damage, disruption of tight junctions, and arrest of proliferation, which threaten male reproductive health. In addition, bisphenols are xenoestrogens, which alter organs and cells functions via agonistic or antagonistic interplay with hormone receptors. In this review, we provide , and evidence that currently available brands of bisphenols impair male reproductive health through their action on testicular cells.

Citing Articles

Interaction of GPER-1 with the endocrine signaling axis in breast cancer.

Molina Calistro L, Arancibia Y, Olivera M, Domke S, Torres R Front Endocrinol (Lausanne). 2025; 16:1494411.

PMID: 39936103 PMC: 11811623. DOI: 10.3389/fendo.2025.1494411.


Integrative transcriptomic profiling uncovers immune and functional responses to bisphenol a across multiple tissues in male mice.

Park Y, Jang M, Ryu D, Lim B, Pathak R, Pang M Anim Cells Syst (Seoul). 2024; 28(1):519-535.

PMID: 39464840 PMC: 11504166. DOI: 10.1080/19768354.2024.2419473.


Impact of Bisphenol A and its alternatives on oocyte health: a scoping review.

Peters A, Ford E, Roman S, Bromfield E, Nixon B, Pringle K Hum Reprod Update. 2024; 30(6):653-691.

PMID: 39277428 PMC: 11532624. DOI: 10.1093/humupd/dmae025.


Bisphenol Analogs Downregulate the Self-Renewal Potential of Spermatogonial Stem Cells.

Kim S, Shin S, Kim S, Jung S, Shin B, Ahn J World J Mens Health. 2024; 43(1):154-165.

PMID: 38606862 PMC: 11704178. DOI: 10.5534/wjmh.230166.


Dynamics of leaching of POPs and additives from plastic in a Procellariiform gastric model: Diet- and polymer-dependent effects and implications for long-term exposure.

Van Hassel L, Scholl G, Eppe G, Poleunisc C, Dupont-Gillain C, Finkelstein M PLoS One. 2024; 19(3):e0299860.

PMID: 38536858 PMC: 10971572. DOI: 10.1371/journal.pone.0299860.


References
1.
Lucas T, Nascimento A, Pisolato R, Pimenta M, Lazari M, Porto C . Receptors and signaling pathways involved in proliferation and differentiation of Sertoli cells. Spermatogenesis. 2014; 4:e28138. PMC: 4160334. DOI: 10.4161/spmg.28138. View

2.
Akingbemi B, Sottas C, Koulova A, Klinefelter G, Hardy M . Inhibition of testicular steroidogenesis by the xenoestrogen bisphenol A is associated with reduced pituitary luteinizing hormone secretion and decreased steroidogenic enzyme gene expression in rat Leydig cells. Endocrinology. 2003; 145(2):592-603. DOI: 10.1210/en.2003-1174. View

3.
Jutte N, Jansen R, Grootegoed J, Rommerts F, Clausen O, VAN DER MOLEN H . Regulation of survival of rat pachytene spermatocytes by lactate supply from Sertoli cells. J Reprod Fertil. 1982; 65(2):431-8. DOI: 10.1530/jrf.0.0650431. View

4.
Joensen U, Jorgensen N, Rajpert-De Meyts E, Skakkebaek N . Testicular dysgenesis syndrome and Leydig cell function. Basic Clin Pharmacol Toxicol. 2008; 102(2):155-61. DOI: 10.1111/j.1742-7843.2007.00197.x. View

5.
Furuya M, Adachi K, Kuwahara S, Ogawa K, Tsukamoto Y . Inhibition of male chick phenotypes and spermatogenesis by Bisphenol-A. Life Sci. 2005; 78(15):1767-76. DOI: 10.1016/j.lfs.2005.08.016. View