Pharmacotherapeutic potential of ginkgetin against polystyrene microplastics-instigated testicular toxicity in rats: A biochemical, spermatological, and histopathological assessment

被引:4
作者
Akbar, Ali [1 ]
Ijaz, Muhammad Umar [1 ]
机构
[1] Univ Agr Faisalabad, Dept Zool Wildlife & Fisheries, Faisalabad, Pakistan
关键词
Ginkgetin; Antioxidant; Polystyrene microplastics; Albino rats; Testicular toxicity; Infertility; OXIDATIVE STRESS; DNA-DAMAGE; SPECTROPHOTOMETRIC ASSAY; FUNCTIONAL INTEGRITY; LIPID-PEROXIDATION; HUMAN SPERMATOZOA; SPERM PARAMETERS; UP-REGULATION; APOPTOSIS; BIFLAVONOIDS;
D O I
10.1007/s11356-023-31662-7
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Polystyrene microplastics (PSMPs) have emerged as a ubiquitous environmental toxicant that affects different organs including testes. Ginkgetin (GNG) is a biflavonoid that shows antioxidant properties. The current research was undertaken to evaluate the ameliorative potential of GNG against PSMPs-instigated testicular damages. Forty-eight albino rats (male) were randomly divided into 4 equal groups: control, PSMPs-treated group (0.01 mgkg-1), GNG + PSMPs-exposed group (25 mgkg-1 + 0.01 mgkg-1), and only GNG-supplemented group (25 mgkg-1). After 56 days of treatment, it was revealed that PSMPs significantly reduced the activity of glutathione peroxidase (GPx), catalase (CAT), superoxide dismutase (SOD), and glutathione reductase (GSR), while concurrently augmented the levels of lipid peroxidation marker, i.e., malondialdehyde (MDA) along with reactive oxygen species (ROS). Rats administered with PSMPs showed a significant reduction in the spermatogenic indices (sperm count, viability, and motility), HOS coiled tail sperm along with increased sperm structural deformities, i.e., tail, head, and mid-piece. Additionally, PSMPs exposure decreased the levels of testosterone, luteinizing (LH), and follicle-stimulating hormones (FSH). Besides, administration of PSMPs reduced the steroidogenic enzymes (13 beta-HSD, StAR, and 17 beta-HSD) and Bcl-2 expression, while augmented the caspase-3 and Bax expression. PSMPs also elevated the levels of inflammatory markers (IL-6, IL-1 beta, TNF-alpha, and NF-kappa B) and activity of COX-2 in the testes. Furthermore, PSMPs treatment induced various histopathological damages in the testes of rats. Therefore, findings of the current study suggested that GNG effectively mitigated the PSMPs-induced testicular toxicity owing to its chemoprotective potential possibly through its anti-inflammatory, antioxidant, anti-apoptotic, and androgenic properties.
引用
收藏
页码:9031 / 9044
页数:14
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