Title: Bisphenol-A analogs induce lower urinary tract dysfunction in male mice.

Authors: Nguyen, J L; Ricke, E A; Liu, T T; Gerona, R; MacGillivray, L; Wang, Z; Timms, B G; Bjorling, D E; Vom Saal, F S; Ricke, W A

Published In Biochem Pharmacol, (2022 Mar)

Abstract: Bisphenol-A (BPA), an estrogenic endocrine disrupting chemical, significantly impacts numerous diseases and abnormalities in mammals. Estrogens are known to play an important role in the biology of the prostate; however, little is known about the role of bisphenols in the etiology of prostate pathologies, including benign prostate hyperplasia (BPH) and associated lower urinary tract dysfunction (LUTD). Bisphenol-F (BPF) and bisphenol-S (BPS) are analogs often used as substitutes for BPA; they are both reported to have in vitro and in vivo estrogenic effects similar to or more potent than BPA. The objective of this study was to assess the role of these bisphenols in the development of LUTD in adult male mice. In adult mice exposed to BPA, BPS or BPF, we examined urinary tract histopathology and physiological events associated with urinary dysfunction. Mice treated with bisphenols displayed increased bladder (p < 0.005) and prostate (p < 0.0001) mass, and there was an increased number of prostatic ducts in the prostatic urethra (p < 0.05) and decreased size of the urethra lumen (p < 0.05) compared to negative controls. After two months of bisphenol exposure, mice displayed notable differences in cystometric tracings compared to controls, consistent with LUTD. Treatment of male mice with all bisphenols also induced voiding dysfunction manifested by detrusor instability and histologic changes in the prostatic urethra of male rodents, consistent with LUTD. Our results implicate BPA and its replacements in the development and progression LUTD in mice and provide insights into the development and progression of BPH/LUTS in men.

PubMed ID: 34979091

MeSH Terms: Animals; Benzhydryl Compounds/blood; Benzhydryl Compounds/chemistry; Benzhydryl Compounds/toxicity*; Estrogens, Non-Steroidal/blood; Estrogens, Non-Steroidal/chemistry; Estrogens, Non-Steroidal/toxicity*; Male; Mice; Mice, Inbred C57BL; Phenols/blood; Phenols/chemistry; Phenols/toxicity*; Prostatic Hyperplasia/blood; Prostatic Hyperplasia/chemically induced*; Prostatic Hyperplasia/pathology; Urologic Diseases/blood; Urologic Diseases/chemically induced*; Urologic Diseases/pathology