Megan V. Alexander , Archana Ayyar , Alexandra W. Gannon , Kristen E. Linares , Sara J. Vincent , Samantha Lowe , Alvin To , Chellakkan S. Blesson
{"title":"The biological effects of bisphenol AF in reproduction and development: What do we know so far?","authors":"Megan V. Alexander , Archana Ayyar , Alexandra W. Gannon , Kristen E. Linares , Sara J. Vincent , Samantha Lowe , Alvin To , Chellakkan S. Blesson","doi":"10.1016/j.reprotox.2025.108857","DOIUrl":null,"url":null,"abstract":"<div><div>Due to the established endocrine-disrupting effects of Bisphenol A (BPA), alternative bisphenols entered the market. Bisphenol AF (BPAF) is now commonly used in the industrial manufacturing of polycarbonate plastics and epoxy resins. However, BPAF’s effects on reproduction and development have not been thoroughly reviewed. We investigated the relationship between BPAF exposure and reproduction and early development. We performed a literature review of studies on BPAF and reproductive physiology. Using keywords, we searched PubMed, Medline, Cochrane Library Database, Embase, and ClinicalTrials.gov for English language literature available until December 2024; we additionally identified and included studies from bibliographies. We included 125 articles, spanning in vitro and in vivo model organism and human studies. BPAF is a selective estrogen receptor modulator and an androgen receptor antagonist and is more potent than BPA. It is detected in urine, blood products, saliva, amniotic fluid, and breast milk. In vitro and in vivo studies demonstrate a spectrum of BPAF-induced endocrine and reproductive changes in both sexes. There is strong evidence of alterations in the hypothalamic-pituitary-gonadal axis and of altered steroidogenesis pathways. Multiple studies using zebrafish, Xenopus, chickens, and rodents, show BPAF’s effects on embryogenesis, morphology, and sexual differentiation. Decreased serum testosterone and impaired spermatogenesis and oocyte viability have been demonstrated. The current literature shows clear disruptive effects of BPAF on reproductive health and embryonic development. Though further investigation is warranted, there is ample converging evidence to support limiting the use of BPAF and other similar bisphenols.</div></div>","PeriodicalId":21137,"journal":{"name":"Reproductive toxicology","volume":"132 ","pages":"Article 108857"},"PeriodicalIF":3.3000,"publicationDate":"2025-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reproductive toxicology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0890623825000280","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"REPRODUCTIVE BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Due to the established endocrine-disrupting effects of Bisphenol A (BPA), alternative bisphenols entered the market. Bisphenol AF (BPAF) is now commonly used in the industrial manufacturing of polycarbonate plastics and epoxy resins. However, BPAF’s effects on reproduction and development have not been thoroughly reviewed. We investigated the relationship between BPAF exposure and reproduction and early development. We performed a literature review of studies on BPAF and reproductive physiology. Using keywords, we searched PubMed, Medline, Cochrane Library Database, Embase, and ClinicalTrials.gov for English language literature available until December 2024; we additionally identified and included studies from bibliographies. We included 125 articles, spanning in vitro and in vivo model organism and human studies. BPAF is a selective estrogen receptor modulator and an androgen receptor antagonist and is more potent than BPA. It is detected in urine, blood products, saliva, amniotic fluid, and breast milk. In vitro and in vivo studies demonstrate a spectrum of BPAF-induced endocrine and reproductive changes in both sexes. There is strong evidence of alterations in the hypothalamic-pituitary-gonadal axis and of altered steroidogenesis pathways. Multiple studies using zebrafish, Xenopus, chickens, and rodents, show BPAF’s effects on embryogenesis, morphology, and sexual differentiation. Decreased serum testosterone and impaired spermatogenesis and oocyte viability have been demonstrated. The current literature shows clear disruptive effects of BPAF on reproductive health and embryonic development. Though further investigation is warranted, there is ample converging evidence to support limiting the use of BPAF and other similar bisphenols.
期刊介绍:
Drawing from a large number of disciplines, Reproductive Toxicology publishes timely, original research on the influence of chemical and physical agents on reproduction. Written by and for obstetricians, pediatricians, embryologists, teratologists, geneticists, toxicologists, andrologists, and others interested in detecting potential reproductive hazards, the journal is a forum for communication among researchers and practitioners. Articles focus on the application of in vitro, animal and clinical research to the practice of clinical medicine.
All aspects of reproduction are within the scope of Reproductive Toxicology, including the formation and maturation of male and female gametes, sexual function, the events surrounding the fusion of gametes and the development of the fertilized ovum, nourishment and transport of the conceptus within the genital tract, implantation, embryogenesis, intrauterine growth, placentation and placental function, parturition, lactation and neonatal survival. Adverse reproductive effects in males will be considered as significant as adverse effects occurring in females. To provide a balanced presentation of approaches, equal emphasis will be given to clinical and animal or in vitro work. Typical end points that will be studied by contributors include infertility, sexual dysfunction, spontaneous abortion, malformations, abnormal histogenesis, stillbirth, intrauterine growth retardation, prematurity, behavioral abnormalities, and perinatal mortality.