食品科学 ›› 2023, Vol. 44 ›› Issue (22): 235-242.doi: 10.7506/spkx1002-6630-20230303-027

• 生物工程 • 上一篇    下一篇

基于非靶向代谢组学研究呋喃西林胁迫下克氏原螯虾体内氨基脲的代谢

陈霞霞, 张祎, 项德胜, 胡诗, 陈雪昌, 张小军   

  1. (1.浙江省海洋水产研究所,浙江省海洋渔业资源可持续利用技术研究重点实验室,浙江 舟山 316021;2.浙江海洋大学食品与药学学院,浙江 舟山 316022;3.浙江大洋兴和食品有限公司,浙江 舟山 316014)
  • 出版日期:2023-11-25 发布日期:2023-12-13
  • 基金资助:
    浙江省基础公益研究计划项目(LGC22C200009)

Untargeted Metabolomics Analysis of Semicarbazide Metabolism in Procambarus clarkii under Nitrofurazone Stress

CHEN Xiaxia, ZHANG Yi, XIANG Desheng, HU Shi, CHEN Xuechang, ZHANG Xiaojun   

  1. (1. Key Laboratory of Sustainable Utilization of Technology Research for Fishery Resources of Zhejiang Province, Zhejiang Marine Fisheries Research Institute, Zhoushan 316021, China; 2. College of Food and Pharmacy, Zhejiang Ocean University, Zhoushan 316022, China; 3. Zhejiang Oceanhealth Food Co. Ltd., Zhoushan 316014, China)
  • Online:2023-11-25 Published:2023-12-13

摘要: 为探究呋喃西林代谢产物氨基脲在甲壳类水产品中的代谢途径,研究不同时间克氏原螯虾(Procambarus clarkii)体内呋喃西林及其代谢物的蓄积情况,同时采用超高效液相色谱-四极杆/静电场轨道阱高分辨质谱代谢组学技术分析氨基脲的代谢组学特征,并通过体外模拟验证实验检验相关通路物质产生氨基脲的可能情况。结果显示,经胁迫后克氏原螯虾肌肉组织中氨基脲含量呈现随时间延长而增多的现象,而呋喃西林含量则先增加后减少再增加。代谢组学显示,经呋喃西林胁迫24 h与4 h样品相比,通过人类代谢数据库共注释到39 种代谢差异物质,其中22 种上调,17 种下调。京都基因与基因组百科全书富集通路表明,胁迫影响牛磺酸及次牛磺酸代谢、精氨酸生物合成、丙氨酸、天冬氨酸和谷氨酸代谢及D-谷氨酰胺和D-谷氨酸代谢相关的通路。验证实验表明牛磺酸、精氨酸、丙氨酸和谷氨酰胺可能是氨基脲代谢途径中的重要物质。

关键词: 呋喃西林;氨基脲;代谢组学;代谢物变化;体外模拟

Abstract: In this study, in order to investigate the metabolic pathway of semicarbazide, a metabolite of nitrofurazone, in crustacean aquatic products, the accumulation of nitrofurazone and its metabolites in Procambarus clarkii was evaluated at different time points, and the metabolomics characteristics of semicarbazide were analyzed by ultra-high performance liquid chromatography-quadrupole/electrostatic field orbitrap high resolution mass spectrometry (UPLC-Q-Exactive-MS). Meanwhile, substances that may be related to semicarbazide production in the metabolic pathway were examined through in vitro simulation test. The results showed that the semicarbazide content in the muscle tissue of P. clarkii increased with increasing nitrofurazone stress period, while the nitrofurazone content initially increased, then decreased and finally increased again. Metabolomics demonstrated that a total of 39 differential metabolites were annotated in samples treated with nitrofurazone for 24 h compared to 4 h, of which 22 metabolites were up-regulated while the remaining 17 were down-regulated. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis suggested that nitrofurazone exposure could affect pathways associated with taurine and hypotaurine metabolism, arginine biosynthesis, alanine, aspartate and glutamate metabolism, and D-glutamine and D-glutamate metabolism. Validation tests confirmed that taurine, arginine, alanine and glutamine might be crucial in the metabolic pathway of semicarbazide.

Key words: nitrofurazone; semicarbazide; metabolomics; metabolite changes; in vivo simulation

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