Effects of DDT and DDE on placental cholinergic receptors

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY Reproductive toxicology Pub Date : 2024-04-12 DOI:10.1016/j.reprotox.2024.108588
Recep Uyar , Yağmur Turgut , H.Tolga Çelik , M. Altay Ünal , Özgür Kuzukıran , Özgür Özyüncü , Ahmet Ceylan , Özge Özgenç Çinar , Ümmü Gülsüm Boztepe , Hilal Özdağ , Ayhan Filazi , Begüm Yurdakök-Di̇kmen
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Abstract

The placental cholinergic system; known as an important factor in intracellular metabolic activities, regulation of placental vascular tone, placental development, and neurotransmission; can be affected by persistent organic pesticides, particularly organochlorine pesticides(OCPs), which can influence various epigenetic regulations and molecular pathways. Although OCPs are legally prohibited, trace amounts of the persistent dichlorodiphenyltrichloroethane(DDT) are still found in the environment, making prenatal exposure inevitable. In this study, the effects of 2,4’-DDT and 4,4’-DDT; and its breakdown product 4,4’-DDE in the environment on placental cholinergic system were evaluated with regards to cholinergic genes. 40 human placentas were screened, where 42,50% (17 samples) were found to be positive for the tested compounds. Average concentrations were 10.44 μg/kg; 15.07 μg/kg and 189,42 μg/kg for 4,4’-DDE; 2,4’-DDT and 4,4’-DDT respectively. RNA-Seq results revealed 2396 differentially expressed genes in positive samples; while an increase in CHRM1,CHRNA1,CHRNG and CHRNA2 genes at 1.28, 1.49, 1.59 and 0.4 fold change were found(p<0028). The increase for CHRM1 was also confirmed in tissue samples with immunohistochemistry. In vitro assays using HTR8/SVneo cells; revealed an increase in mRNA expression of CHRM1, CHRM3 and CHRN1 in DDT and DDE treated groups; which was also confirmed through western blot assays. An increase in the expression of CHRM1,CHRNA1, CHRNG(p<0001) and CHRNA2(p<0,05) were found from the OCPs exposed and non exposed groups.The present study reveals that intrauterine exposure to DDT affects the placental cholinergic system mainly through increased expression of muscarinic receptors. This increase in receptor expression is expected to enhance the sensitivity of the placental cholinergic system to acetylcholine.

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滴滴涕和二苯醚对胎盘胆碱能受体的影响
众所周知,胎盘胆碱能系统是细胞内代谢活动、胎盘血管张力调节、胎盘发育和神经传导的重要因素,它可能受到持久性有机杀虫剂,尤其是有机氯杀虫剂(OCPs)的影响,从而影响各种表观遗传调节和分子通路。虽然有机氯农药已被依法禁止使用,但环境中仍存在微量的持久性二氯二苯基三氯乙烷(DDT),因此产前接触这种农药是不可避免的。本研究通过胆碱能基因评估了环境中 2,4'-DDT 和 4,4'-DDT 及其分解产物 4,4'-DDE 对胎盘胆碱能系统的影响。对 40 个人类胎盘进行了筛查,发现 42.50%(17 个样本)的受试化合物呈阳性。4,4'-DDE、2,4'-DDT 和 4,4'-DDT 的平均浓度分别为 10.44 微克/千克、15.07 微克/千克和 189,42 微克/千克。RNA-Seq 结果显示,阳性样品中有 2396 个差异表达基因,其中 CHRM1、CHRNA1、CHRNG 和 CHRNA2 基因的表达量分别增加了 1.28、1.49、1.59 和 0.4 倍(p<0028)。组织样本中的免疫组化也证实了 CHRM1 的增加。使用 HTR8/SVneo 细胞进行的体外检测显示,在 DDT 和 DDE 处理组中,CHRM1、CHRM3 和 CHRN1 的 mRNA 表达量增加;这一点也通过 Western 印迹检测得到了证实。本研究表明,宫内接触滴滴涕主要通过增加毒蕈碱受体的表达来影响胎盘胆碱能系统。受体表达的增加预计会提高胎盘胆碱能系统对乙酰胆碱的敏感性。
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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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