Effect of fish oil supplementation on histological changes, apoptosis and oxidative stress of rat placenta against formaldehyde-induced toxicity

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY Reproductive toxicology Pub Date : 2024-08-12 DOI:10.1016/j.reprotox.2024.108688
Kaveh Khazaeel , Sameerah Abdulzahra Daaj , Reza Ranjbar , Jamal Nourinezhad , Mohammad Reza Tabandeh
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Abstract

Formaldehyde (FA) as a common organic compound has been shown to cause placental dysfunction and fetal defects. The potential benefits of fish oil (FOil) in protecting placental structures are attributed to its antioxidant properties. This study aimed to explore the preventive role of FOil in mitigating the adverse effects of FA in pregnant rats. Thirty pregnant Wistar rats were randomly categorized into five groups of control, sham (Normal saline; Orally and intraperitoneally), FOil (0.5 ml/day; Orally), FA (5 mg/kg/bw; intraperitoneally), FA+FOil. The treatment period was from day 0–20 of pregnancy. On the 20th day of pregnancy, placental morphometric parameters were measured. The histological and histochemical analyses were performed using H&E and PAS staining, respectively. Also, the placenta tissue was analyzed for oxidative stress biomarkers, p-53 protein levels, and the expression of caspase-3 gene. The administration of FA led to a significant decrease in the weight, diameter, and thickness of the placenta, as well as a decrease in the thickness of the decidua layer, junctional and labyrinth zone, and the number of trophoblast giant cells in rat placentas. FA led to a significant increase in placental p-53 protein levels, caspase-3 expression, and oxidative stress biomarkers. Administration of FOil to pregnant rats treated with FA led to a significant decrease in morphometric and histological changes, oxidative stress, and the expression of genes associated with apoptosis. The findings suggest that the administration of FOil to FA-treated pregnant rats can protect placental histopathological changes by enhancing the activity of the antioxidant enzymes.

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补充鱼油对大鼠胎盘组织学变化、细胞凋亡和氧化应激对甲醛诱导毒性的影响
甲醛(FA)作为一种常见的有机化合物,已被证明会导致胎盘功能障碍和胎儿缺陷。鱼油(FOil)在保护胎盘结构方面的潜在益处归功于其抗氧化特性。本研究旨在探讨鱼油在减轻 FA 对怀孕大鼠不利影响方面的预防作用。30 只怀孕的 Wistar 大鼠被随机分为五组,即对照组、假组(正常生理盐水;口服和腹腔注射)、鱼油组(0.5 毫升/天;口服)、FA 组(5 毫克/千克/体重;腹腔注射)和 FA+FOil 组。治疗期为妊娠的第 0 天至第 20 天。妊娠第 20 天,测量胎盘形态参数。分别使用 H&E 和 PAS 染色法进行组织学和组织化学分析。此外,还对胎盘组织的氧化应激生物标志物、p-53 蛋白水平和 Caspase-3 基因的表达进行了分析。给大鼠胎盘服用 FA 后,胎盘的重量、直径和厚度显著减少,蜕膜层、连接区和迷宫区的厚度以及滋养层巨细胞的数量也显著减少。FA 导致胎盘 p-53 蛋白水平、caspase-3 表达和氧化应激生物标志物显著增加。给接受过 FA 治疗的妊娠大鼠服用 FOil 后,形态计量学和组织学变化、氧化应激以及与细胞凋亡相关的基因表达均明显减少。研究结果表明,给接受过 FA 处理的妊娠大鼠服用 FOil 可通过增强抗氧化酶的活性来保护胎盘组织病理学变化。
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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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