Exposure of Porcine Oocytes to Methylparaben During In Vitro Maturation Alters the Expression of Genes Involved in Cumulus Cell Expansion and Steroidogenesis, Decreasing Hyaluronic Acid and Progesterone Synthesis.

IF 2.7 4区 医学 Q3 TOXICOLOGY Journal of Applied Toxicology Pub Date : 2024-11-26 DOI:10.1002/jat.4727
Adyeni Barajas-Salinas, Iván Bahena, Juan José Rodríguez-Mercado, Lizbeth Juárez-Rojas, Miguel Betancourt, Elivier Núñez-Macías, Yenny Ramírez-Jara, Alma López, Eduardo Casas, Edmundo Bonilla, Zayil Salazar, Fahiel Casillas
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Abstract

Parabens are widely used because of their antimicrobial properties in drugs, cosmetics, and food; however, it has been reported that methylparaben may adversely influence female reproduction. Methylparaben decreases oocyte in vitro maturation at a maturation inhibition concentration 50 of 780.31 μM but also decreases oocyte viability at a lethal concentration 50 of 2028.38 μM. Additionally, parabens are endocrine disruptors, affecting steroidogenesis as well as cumulus cell expansion. Therefore, the aim of this study was to elucidate some of the mechanisms by which methylparaben alters cumulus cell expansion and decreases oocyte maturation through the evaluation of gene expression related to cumulus cell expansion, hyaluronic acid, and progesterone synthesis. For this, oocytes were exposed to different methylparaben concentrations of 0 (control), 650, 780, and 1000 μM for 20 and 44 h of in vitro maturation. The cumulus cell expansion rates, maturation rates, gene expression rates, and hyaluronic acid and progesterone concentrations were revaluated after 20 and 44 h of culture. At sublethal concentrations, methylparaben decreased in vitro maturation as well as cumulus cell expansion at 44 h. Additionally, methylparaben decreased the expression of Has2 and Cd44 at 20 and 44 h of maturation. The expression levels of Stard1, Cyp11a1, and Hsd3b1 were also altered by methylparaben exposure at 20 and 44 h of maturation, suggesting its role as an endocrine disruptor. Hyaluronic acid and progesterone concentrations in the culture medium decreased at 20 and 44 h. These findings could partially explain some of the mechanisms by which methylparaben alters female fertility.

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对羟基苯甲酸酯因其抗菌特性而被广泛应用于药物、化妆品和食品中;但有报告称,甲基对羟基苯甲酸酯可能会对女性生殖产生不利影响。甲基苯甲酸酯会降低卵母细胞的体外成熟度,其成熟抑制浓度 50 为 780.31 μM,但也会降低卵母细胞的存活率,其致死浓度 50 为 2028.38 μM。此外,对羟基苯甲酸酯类还是一种内分泌干扰物,会影响类固醇的生成和精母细胞的扩张。因此,本研究的目的是通过评估与积层细胞扩增、透明质酸和孕酮合成有关的基因表达,阐明苯甲酸甲酯改变积层细胞扩增和降低卵母细胞成熟度的一些机制。为此,将卵母细胞暴露于不同浓度的尼泊金(0(对照组)、650、780 和 1000 μM)中,体外成熟 20 和 44 小时。在培养 20 和 44 小时后,对精原细胞扩增率、成熟率、基因表达率以及透明质酸和孕酮浓度进行了重新评估。在亚致死浓度下,甲基对羟基苯甲酸甲酯降低了体外成熟度,也降低了 44 小时后的精母细胞扩增率。此外,甲基对羟基苯甲酸甲酯还降低了 20 小时和 44 小时成熟过程中 Has2 和 Cd44 的表达。Stard1、Cyp11a1和Hsd3b1的表达水平也因甲基对羟基苯甲酸酯在成熟20和44小时时的暴露而改变,这表明甲基对羟基苯甲酸酯是一种内分泌干扰物。培养基中的透明质酸和孕酮浓度在 20 和 44 小时后有所下降。这些发现可以部分解释对羟基苯甲酸甲酯改变女性生育能力的一些机制。
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来源期刊
CiteScore
7.00
自引率
6.10%
发文量
145
审稿时长
1 months
期刊介绍: Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.
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Exposure of Porcine Oocytes to Methylparaben During In Vitro Maturation Alters the Expression of Genes Involved in Cumulus Cell Expansion and Steroidogenesis, Decreasing Hyaluronic Acid and Progesterone Synthesis. Behavioural, Teratogenic and Genotoxic Effects of Antibacterial Compounds, Triclocarban and Triclosan, in Hydra vulgaris. Ergothioneine Ameliorates Liver Fibrosis by Inhibiting Glycerophospholipids Metabolism and TGF-β/Smads Signaling Pathway: Based on Metabonomics and Network Pharmacology. A Rapid Quantitative Assessment Method for Liver Damage Effects of Compounds Based on Zebrafish Liver Partition Area Ratio. Association of Stress Defense System With Fine Particulate Matter Exposure: Mechanism Analysis and Application Prospects.
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