亚急性接触三丁基锡和汞的混合物会损害生殖轴功能,加剧卵巢功能过早衰竭,降低雌性大鼠的生育能力。

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY
Cidalia de F. Januario , Charles S. Da Costa , Flavia C.F. Dos Santos , Leandro Miranda-Alves , Bruna S. Correa , Maria T.W.D. Carneiro , Jones B. Graceli
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引用次数: 0

摘要

三丁基锡(TBT)和汞(Hg)是干扰内分泌的化学物质,单独使用会引起生殖系统并发症。然而,人们对接触三丁基锡化合物和汞的混合物对生殖系统的影响还不甚了解。我们假设,接触三丁基锡化合物和汞的混合物会改变下丘脑-垂体-性腺轴(HPG)的功能。雌性大鼠每天接触这种混合物 15 天,之后对组织中的化学积累、形态、激素水平、炎症、纤维化和生殖器官中的蛋白质表达进行评估。在 TBT-Hg 大鼠的血清、HPG 轴和子宫中检测到锡(Sn)和汞含量的增加。TBT-Hg 大鼠的发情周期不规律。TBT-Hg 大鼠的促性腺激素释放激素(GnRH)蛋白表达和卵泡刺激素(FSH)水平升高,黄体生成素(LH)水平降低。研究还发现,大鼠的卵巢储备功能、前卵泡、黄体(CL)数量和雌激素水平降低,闭锁卵泡和囊性卵泡增多,这表明三丁基锡化合物汞暴露会加剧卵巢早衰(POI)特征。此外,TBT-汞大鼠的卵巢肥大细胞数量、炎症标志物 IL-6 的表达和胶原沉积都有所增加。在 TBT-Hg 大鼠的子宫中观察到腺体凋亡和腺体数量减少。TBT-Hg 大鼠 90 天内每窝产仔数减少,表明生育能力受损。血清和卵巢 Sn 含量与卵巢汞含量、卵巢储备功能和 CL 数量之间存在很强的负相关。总之,这些数据表明,接触三丁基锡化合物和汞会导致 HPG 轴异常,加剧 POI 特征并降低雌性大鼠的生育能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Subacute exposure to a mixture of tributyltin plus mercury impairs reproductive axis function, exacerbating premature ovarian insufficiency features and reducing fertility in female rats

Tributyltin (TBT) and mercury (Hg) are endocrine-disrupting chemicals that individually cause reproductive complications. However, the reproductive consequences of exposure to a mixture of TBT plus Hg are not well known. We hypothesized that exposure to a mixture of TBT plus Hg would alter hypothalamic-pituitary-gonadal (HPG) axis function. Female rats were exposed to this mixture daily for 15 days, after which chemical accumulation in the tissues, morphology, hormone levels, inflammation, fibrosis, and protein expression in the reproductive organs were assessed. Increases in tin (Sn) and Hg levels were detected in the serum, HPG axis, and uterus of TBT-Hg rats. TBT-Hg rats exhibited irregular estrous cycles. TBT-Hg rats showed an increase in gonadotropin-releasing hormone (GnRH) protein expression and follicle-stimulating hormone (FSH) levels and a reduction in luteinizing hormone (LH) levels. Reduced ovarian reserve, antral follicles, corpora lutea (CL) number, and estrogen levels and increased atretic and cystic follicles were found, suggesting that TBT-Hg exposure exacerbated premature ovarian insufficiency (POI) features. Furthermore, TBT-Hg rats exhibited increased ovarian mast cell numbers, expression of the inflammatory markers IL-6 and collagen deposition. Apoptosis and reduced gland number were observed in the uteri of TBT-Hg rats. A reduction in the number of pups/litter for 90 days was found in TBT-Hg rats, suggesting impaired fertility. Strong negative correlations were found between serum and ovarian Sn levels and ovarian Hg levels and ovarian reserve and CL number. Collectively, these data suggest that TBT plus Hg exposure leads to abnormalities in the HPG axis, exacerbating POI features and reducing fertility in female rats.

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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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