Quaternary ammonium compound exposure causes infertility by altering endocrine signaling and gametogenesis

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY Reproductive toxicology Pub Date : 2024-12-07 DOI:10.1016/j.reprotox.2024.108817
Zachary A. Kirkpatrick , Vanessa E. Melin , Terry C. Hrubec
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Abstract

Quaternary ammonium compounds (QACs) are common substances utilized in cleaners, ophthalmic solutions, swimming pool treatments, cosmetics, and other consumer goods. Previous studies have shown that QAC exposure causes infertility in both male and female mice. Based on these studies, we hypothesized that oral QAC exposure negatively impacts male and female reproduction through changes in physiologic and endocrine mechanisms rather than direct toxicity to gametes. Endocrine disruption was assessed by evaluating luteinizing hormone (LH) and follicle stimulating hormone (FSH) concentrations in male and female mice exposed orally throughout gestation and lactation, and by changes in estrogen and progesterone in in orally exposed females throughout pregnancy. Sperm functionality and spermatogenesis were assessed by in vitro fertilization; while Sertoli cell homeostasis was evaluated by determining cellular metabolism, cell cycle progression and blood-testes barrier (BTB) permeability. QAC exposure decreased LH, and FSH concentrations in both males and females, and decreased progesterone and estrogen concentrations during pregnancy. QACs significantly decreased Sertoli cell metabolism at 0.0005 % ADBAC+DDAC well before disruption of the BTB at 0.01 %. Fertilization was not affected 24 h after exposure but was decreased after a 10 day rest period suggesting a disruption in spermatogenesis rather than direct toxicity to sperm. Lastly, QAC exposure altered Sertoli cell cycling with a G2/M cycle arrest. While the effect of QAC exposure on humans is unknown, implications from the in vivo and in vitro studies are concerning given the rise in infertility rates and increased reliance on assisted reproductive technologies along with ubiquitous exposure to QACs.
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季铵化合物暴露通过改变内分泌信号和配子发生导致不育。
季铵化合物(QACs)是清洁剂、眼科溶液、游泳池护理、化妆品和其他消费品中常用的物质。先前的研究表明,接触QAC会导致雄性和雌性小鼠不孕。基于这些研究,我们假设口服QAC暴露通过生理和内分泌机制的改变而不是直接对配子产生毒性,从而对男性和女性的生殖产生负面影响。通过在整个妊娠期和哺乳期口服暴露的雄性和雌性小鼠中黄体生成素(LH)和促卵泡激素(FSH)的浓度,以及在整个妊娠期口服暴露的雌性小鼠中雌激素和黄体酮的变化来评估内分泌干扰。通过体外受精评估精子功能和精子发生;通过测定细胞代谢、细胞周期进展和血睾丸屏障(BTB)通透性来评估支持细胞稳态。妊娠期暴露于QAC可降低男性和女性的LH和FSH浓度,并降低孕酮和雌激素浓度。当ADBAC+DDAC浓度为0.0005%时,QACs显著降低了支持细胞的代谢,而当ADBAC+DDAC浓度为0.01%时,BTB则被破坏。暴露24小时后,受精不受影响,但在休息10天后,受精减少,这表明精子发生受到干扰,而不是直接对精子产生毒性。最后,QAC暴露改变了支持细胞周期,出现G2/M周期阻滞。虽然QAC暴露对人类的影响尚不清楚,但鉴于不孕率的上升和对辅助生殖技术的依赖增加以及QAC的普遍暴露,体内和体外研究的影响令人担忧。
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来源期刊
Reproductive toxicology
Reproductive toxicology 生物-毒理学
CiteScore
6.50
自引率
3.00%
发文量
131
审稿时长
45 days
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.
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