赵淑琦, 张平, 王铮, 张济明, 常秀丽, 黄沪涛, 周志俊. 基于代谢组学揭示氟咯草酮对小鼠睾丸代谢及炎症反应的影响J. 职业卫生与应急救援, 2025, 43(6): 812-819. DOI: 10.16369/j.oher.issn.1007-1326.2025.250130
引用本文: 赵淑琦, 张平, 王铮, 张济明, 常秀丽, 黄沪涛, 周志俊. 基于代谢组学揭示氟咯草酮对小鼠睾丸代谢及炎症反应的影响J. 职业卫生与应急救援, 2025, 43(6): 812-819. DOI: 10.16369/j.oher.issn.1007-1326.2025.250130
ZHAO Shuqi, ZHANG Ping, WANG Zeng, ZHANG Jiming, CHANG Xiuli, HUANG Hutao, ZHOU Zhijun. Metabolomics-based study on effects of flurochloridone on testicular inflammatory injury in mice and its mechanismJ. Occupational Health and Emergency Rescue, 2025, 43(6): 812-819. DOI: 10.16369/j.oher.issn.1007-1326.2025.250130
Citation: ZHAO Shuqi, ZHANG Ping, WANG Zeng, ZHANG Jiming, CHANG Xiuli, HUANG Hutao, ZHOU Zhijun. Metabolomics-based study on effects of flurochloridone on testicular inflammatory injury in mice and its mechanismJ. Occupational Health and Emergency Rescue, 2025, 43(6): 812-819. DOI: 10.16369/j.oher.issn.1007-1326.2025.250130

基于代谢组学揭示氟咯草酮对小鼠睾丸代谢及炎症反应的影响

Metabolomics-based study on effects of flurochloridone on testicular inflammatory injury in mice and its mechanism

  • 摘要:
    目的 通过代谢组学揭示氟咯草酮(FLC)暴露对小鼠睾丸组织代谢及炎症反应的影响。
    方法 选择6~8周龄雄性C57BL/6小鼠,随机分为对照组和3、15、75、375 mg/(kg·d)FLC染毒组。苏木精-伊红(HE)染色观察小鼠睾丸病理变化;应用超高效液相色谱-质谱和生信分析,检测睾丸组织代谢谱,并筛选差异代谢物(DMs);通过Metaboanlyst对DMs进行代谢物富集分析和通路富集分析,按FLC染毒剂量不同,定量分析显著富集的代谢途径中的DMs。酶联免疫吸附法(ELISA)检测肿瘤坏死因子α(TNF-α)和白细胞介素1β(IL-1β)的变化。
    结果 375 mg/(kg·d)FLC染毒28 d后,小鼠睾丸生精小管发生明显病理性损伤。FLC染毒引起小鼠睾丸组织代谢扰动,筛选出的73种DMs大多属于脂质和羧酸类,主要包括脂肪酸及其复合物、吲哚羧酸、类固醇类等。DMs主要富集在核黄素代谢、鞘脂代谢、花生四烯酸代谢和酮体代谢等途径。对DMs进行量化分析,与对照组相比,核黄素水平在375 mg/(kg·d)FLC染毒组显著降低(P < 0.000 1),鞘氨醇、前列腺素和3-羟基丁酸水平在375 mg/(kg·d)FLC染毒组均显著升高(P < 0.05)。与对照组相比,375 mg/(kg·d)FLC染毒组中促炎细胞因子TNF-α和IL-1β水平均显著升高(P < 0.01)。
    结论 FLC暴露引起小鼠睾丸病理损伤,改变了睾丸组织的代谢谱,主要影响其脂质代谢和性激素代谢,提示睾丸发生炎症反应,为FLC睾丸毒性机制提供了新的见解。

     

    Abstract:
    Objective To investigate the effects of flurochloridone (FLC) exposure on testicular metabolism and inflammation in mice using metabolomics technology.
    Methods Male C57BL/6 mice aged 6 to 8 weeks were randomly divided into a control group and FLC-exposed groups with doses of 3, 15, 75, and 375 mg/(kg·d). Hematoxylin-eosin(HE) staining was used to observe pathological changes in mouse testes. Ultra performance liquid chromatography-mass spectrometry(UPLC-MS) combined with bioinformatics analysis was applied to detect the testicular metabolic profile and screen differential metabolites(DMs). Metabolite set enrichment analysis and pathway enrichment analysis of DMs were performed using MetaboAnalyst, and DMs involved in significantly enriched metabolic pathways were quantitatively analyzed according to different FLC exposure doses. The changes in tumor necrosis factor-α(TNF-α) and interleukin-1β(IL-1β) were detected by double-antibody enzyme-linked immunosorbent assay(ELISA).
    Results After 28 days of exposure to 375 mg/(kg·d) FLC, obvious pathological damage was observed in the seminiferous tubules of mouse testes. FLC exposure caused metabolic disturbances in mouse testicular tissue, and the 73 screened DMs were mostly lipids and carboxylic acids, mainly including fatty acids and their complexes, indole carboxylic acids, and steroids. These DMs were mainly enriched in metabolic pathways such as riboflavin metabolism, sphingolipid metabolism, arachidonic acid metabolism, and ketone body metabolism. Quantitative analysis of DMs showed that riboflavin levels were significantly decreased in the 375 mg/(kg·d) FLC-exposed group (P < 0.000 1). The levels of sphingosine, prostaglandins, and 3-hydroxybutyric acid were significantly increased in the 375 mg/(kg·d) FLC-exposed group (P < 0.05). Additionally, the levels of pro-inflammatory factors TNF-α and IL-1β were significantly elevated in the 375 mg/(kg·d) FLC-exposed group (P < 0.01).
    Conclusions FLC exposure could cause pathological damage to mouse testes and alter the testicular metabolic profile, mainly affecting lipid metabolism and sex hormone metabolism, which suggested the occurrence of testicular inflammatory responses. This study provided new insights into the mechanism of FLC-induced testicular toxicity.

     

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