Protective effect of Petroselinum crispum methanolic extract against acrylamide-induced reproductive toxicity in male rats through NF-ĸB, kinesin, steroidogenesis pathways

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY Reproductive toxicology Pub Date : 2024-04-16 DOI:10.1016/j.reprotox.2024.108586
Ahmed M.E. Shipa , Khaled A. Kahilo , Samir A. Elshazly , Ehab S. Taher , Nasr E. Nasr , Badriyah S. Alotaibi , Essam A. Almadaly , Mona Assas , Walied Abdo , Tarek K. Abouzed , Abdulati Elsanusi Salem , Damla Kirci , Hesham R. El-Seedi , Mohamed S. Refaey , Nermin I. Rizk , Mustafa Shukry , Doaa A. Dorghamm
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Abstract

This study examined the protective effects of a Petroselinum crispum (P. crispum) methanolic extract on reproductive dysfunction induced by acrylamide in male rats. A total of 40 rats were divided into four groups (n=10). The control group received distilled water, the acrylamide group received 10 mg/kg of acrylamide, the P. crispum group received 100 mg/kg of P. crispum extract, and the combined group was pretreated with P. crispum for two weeks before co-administration of P. crispum and acrylamide. All administrations were administered orally using a gastric tube for eight weeks. Acrylamide decreased testosterone levels but did not affect levels of FSH or LH. It also increased testicular levels of (MDA) malondialdehyde and reduced activity of (SOD) superoxide dismutase and impairment of sperm parameters. Furthermore, the administration of acrylamide resulted in an elevation of tumor necrosis factor-alpha (TNF-α) levels and a reduction in the levels of steroidogenic acute regulatory protein (STAR) and cytochrome P450scc (P450scc). Acrylamide negatively affected the histopathological outcomes, Johnsen's score, the diameter of seminiferous tubules, and the thickness of the germinal epithelium. It also upregulated the expression of NF-ĸB P65 and downregulated the expression of kinesin motor protein. In contrast, treatment with P. crispum extract restored the levels of antioxidant enzymes, improved sperm parameters, and normalized the gene expression of TNF-α, IL-10, IL-6, iNOS, NF-ĸB, STAR, CYP17A1, 17β-HSD and P450scc. It also recovered testicular histological parameters and immunoexpression of NF-ĸB P65 and kinesin altered by acrylamide. P. crispum showed protective effects against acrylamide-induced reproductive toxicity by suppressing oxidative damage and inflammatory pathways.

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脆皮草甲醇提取物通过 NF-ĸB、驱动蛋白和类固醇生成途径对丙烯酰胺诱导的雄性大鼠生殖毒性具有保护作用
本研究探讨了清脆石蒜甲醇提取物对丙烯酰胺诱导的雄性大鼠生殖功能障碍的保护作用。共有 40 只大鼠被分为四组(n=10)。对照组接受蒸馏水,丙烯酰胺组接受每公斤 10 毫克的丙烯酰胺,清脆木组接受每公斤 100 毫克的清脆木提取物,而联合组在同时服用清脆木和丙烯酰胺之前先用清脆木预处理两周。所有给药均使用胃管口服,为期八周。丙烯酰胺会降低睾酮水平,但不会影响 FSH 或 LH 水平。丙烯酰胺还增加了睾丸中丙二醛的含量,降低了超氧化物歧化酶的活性,损害了精子参数。此外,丙烯酰胺还导致肿瘤坏死因子-α(TNF-α)水平升高,类固醇生成急性调节蛋白(STAR)和细胞色素 P450scc(P450scc)水平降低。丙烯酰胺对组织病理学结果、Johnsen评分、曲细精管直径和生精上皮厚度有负面影响。丙烯酰胺还上调了 NF-ĸB P65 的表达,并下调了驱动蛋白运动蛋白的表达。与此相反,清脆木提取物能恢复抗氧化酶的水平,改善精子参数,并使 TNF-α、IL-10、IL-6、iNOS、NF-ĸB、STAR、CYP17A1、17β-HSD 和 P450scc 的基因表达正常化。它还能恢复睾丸组织学参数以及丙烯酰胺改变的 NF-ĸB P65 和驱动蛋白的免疫表达。清脆木通过抑制氧化损伤和炎症途径,对丙烯酰胺诱导的生殖毒性具有保护作用。
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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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