褪黑素和白藜芦醇可减轻双酚 A 在子宫内膜有机体中诱导的分子和代谢毒性。

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY Reproductive toxicology Pub Date : 2024-06-05 DOI:10.1016/j.reprotox.2024.108628
Mariam M. Abady , Islam M. Saadeldin , Ayeong Han , Seonggyu Bang , Heejae Kang , Dong Wook Seok , Ha-Jeong Kwon , Jongki Cho , Ji-Seon Jeong
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引用次数: 0

摘要

双酚 A(BPA)是一种广泛存在的环境污染物,它对子宫内膜的生理功能具有破坏性影响,因而备受关注。相比之下,褪黑素(MT)和白藜芦醇(RSV)因其对双酚 A 引起的损伤具有潜在的保护作用而备受关注。考虑到动物试验的有效性和伦理问题,子宫内膜器官组织(模拟子宫内膜的三维模型)是揭示环境因素对生殖健康影响的重要工具。本研究旨在全面描述猪子宫内膜器官组织对双酚 A 的形态、分子和代谢反应,并评估 MT 和 RSV 的潜在保护作用。制备猪子宫,用胶原酶消化,与 Matrigel 混合,在 38°C 和 5% CO2 条件下培养。传代过程包括通过胰蛋白酶-EDTA处理解离和亚培养。培养基每 2-3 天更换一次。为了研究环境对生殖健康的影响,用双酚 A(0.5µM)、MT(含/不含双酚 A,0.1µM)和/或 RSV(10µM)处理子宫内膜器官组织。通过基因表达、Western 印迹、免疫荧光染色和代谢物分析等多种分子筛选方法,评估了双酚 A、MT 和 RSV 对子宫内膜有机体细胞活力、形态、生殖能力和代谢改变的影响。不出所料,双酚A会诱导有机体的结构和分子破坏,影响细胞骨架蛋白、Wnt/β-catenin信号传导和上皮/间质标记物。它引发了氧化应激和细胞凋亡途径,改变了 miRNA 的表达,并破坏了内源性大麻素系统。与对照组相比,双酚 A 处理组的葡萄糖、半乳糖和必需氨基酸水平增加或减少了约 1.5 至 3 倍(P 值 < 0.05),表明代谢发生了变化。此外,MT 和 RSV 处理组表现出保护作用,减轻了双酚 A 诱导的多途径紊乱。我们的研究首次以子宫内膜有机体为模型,加深了人们对环境对生殖健康影响的理解。
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Melatonin and resveratrol alleviate molecular and metabolic toxicity induced by Bisphenol A in endometrial organoids

Bisphenol A (BPA), a widespread environmental contaminant, poses concerns due to its disruptive effects on physiological functions of the uterine endometrium. In contrast, melatonin (MT) and Resveratrol (RSV) are under scrutiny for their potential protective roles against BPA-induced damage. For the efficacy and ethical concerns in the animal test, endometrial organoids, three-dimensional models mimicking endometrium, serve as crucial tools for unraveling the impact of environmental factors on reproductive health. This study aimed to comprehensively characterize the morphological, molecular and metabolic responses of porcine endometrial organoids to BPA and assess the potential protective effects of MT and RSV. Porcine uteri were prepared, digested with collagenase, mixed with Matrigel, and incubated at 38°C with 5 % CO2. Passaging involved dissociation through trypsin-EDTA treatment and subculturing. The culture medium was refreshed every 2–3 days. To investigate the environmental impact on reproductive health, endometrial organoids were treated with BPA (0.5 µM), MT (with/without BPA at 0.1 µM), and/or RSV (10 µM). Various molecular screening using gene expression, western blotting, immunofluorescence staining, and metabolites profiling were assessed the effects of BPA, MT, and RSV in terms of cell viability, morphology, reproductivity, and metabolism alteration in the endometrial organoids. As expected, BPA induced structural and molecular disruptions in organoids, affecting cytoskeletal proteins, Wnt/β-catenin signaling, and epithelial/mesenchymal markers. It triggered oxidative stress and apoptotic pathways, altered miRNA expression, and disrupted the endocannabinoid system. The level of glucose, galactose, and essential amino acids were increased or decreased by approximately 1.5–3 times in BPA-treated groups compared to the control groups (p-value < 0.05), indicating metabolic changes. Moreover, MT and RSV treated groups exhibited protective effects, mitigating BPA-induced disruptions across multiple pathways. For the first time, our study models endometrial organoids, advancing understanding of environmental impacts on reproductive health.

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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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