Wang Yueyang, Bai Yichen, Wang Yi, Cai Yan
Department of Obstetrics, The Fourth Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
College of Animal Science and Technology, Northeast Agricultural University, Harbin 150030, China.
Metabolites. 2025 May 20;15(5):339. doi: 10.3390/metabo15050339.
Cadmium (Cd) is a highly toxic heavy metal. There are very few studies about the effects of Cd on reproductive health and metabolism, and even fewer on metabolic disorders in the uterus of mice in labor. This study is the first to establish a model of Cd exposure in the uterus of laboring mice and investigate the underlying metabolic mechanisms through transcriptomic analysis. Pregnant mice received intraperitoneal injections of CdCl (1.5 mg/kg) on gestational days 12.5, 14.5, and 16.5 were set up as the experimental group (Cd group), and pregnant mice injected with saline were set up as the control group (CT group). A total of 738 differentially expressed genes (DEGs) were screened using DESeq2 software, including 326 upregulated genes and 412 downregulated genes. Through enrichment databases including the KEGG, GO, Reactome, and PANTHER, we identified 76 metabolism-related DEGs and performed protein-protein interaction (PPI) network analysis. The PPI results were visualized using Cytoscape software and further analyzed, with 18 hub genes (maximum clique centrality score > 10) identified through the MCC algorithm of the Cytohubba plugin. The results showed that the highest-scoring hub genes included , , , , , and , which are involved in mitochondrial energy metabolism. The remaining lower-scoring hub genes were primarily associated with coagulation processes. Pathway analysis revealed hub genes predominantly involved in oxidative phosphorylation, complement and coagulation cascades, the cGMP-PKG signaling pathway, and thermogenesis. This study successfully established a Cd exposure-induced uterine injury model, providing valuable references for human reproductive health research.
镉(Cd)是一种剧毒重金属。关于镉对生殖健康和新陈代谢影响的研究非常少,而关于分娩期小鼠子宫代谢紊乱的研究更少。本研究首次建立了分娩期小鼠子宫镉暴露模型,并通过转录组分析研究其潜在的代谢机制。将在妊娠第12.5、14.5和16.5天腹腔注射氯化镉(1.5毫克/千克)的怀孕小鼠设为实验组(镉组),将注射生理盐水的怀孕小鼠设为对照组(CT组)。使用DESeq2软件共筛选出738个差异表达基因(DEG),其中上调基因326个,下调基因412个。通过包括KEGG、GO、Reactome和PANTHER在内的富集数据库,我们鉴定出76个与代谢相关的DEG,并进行了蛋白质-蛋白质相互作用(PPI)网络分析。使用Cytoscape软件对PPI结果进行可视化并进一步分析,通过Cytohubba插件的MCC算法鉴定出18个枢纽基因(最大团中心性得分>10)。结果表明,得分最高的枢纽基因包括 、 、 、 、 和 ,它们参与线粒体能量代谢。其余得分较低的枢纽基因主要与凝血过程相关。通路分析显示枢纽基因主要参与氧化磷酸化、补体和凝血级联反应、cGMP-PKG信号通路和产热。本研究成功建立了镉暴露诱导的子宫损伤模型,为人类生殖健康研究提供了有价值的参考。