ARTICLE
20 September 2026

消渴固肾方干预2型糖尿病模型大鼠血清代谢重塑的非靶向代谢组学研究

争敏 赵1 ,  红朝 齐1 ,  欣 李1 ,  佳丽 吴1 ,  晓芹 吴1 ,  靓 郑1
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1 海南省海口市中医医院内分泌风湿肾病科, 中国
MRP 2026 , 4(9), 130–134; https://doi.org/10.61369/MRP.2026090026
© 2026 by the Author(s). Licensee Art and Technology, USA. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution -Noncommercial 4.0 International License (CC BY-NC 4.0) ( https://creativecommons.org/licenses/by-nc/4.0/ )
Abstract

目的:基于LC-MS 非靶向血清代谢组学,解析消渴固肾方对高脂饮食联合链脲佐菌素诱导2型糖尿病大鼠血清代谢重塑的作用。方法:设正常、模型、消渴固肾方低/ 中/ 高剂量、阳性对照及QC 组,行LC-MS 采集、差异分析、PCA/PLS-DA、KEGG 富集及WGCNA 分析。结果:纳入34个样本,获690个代谢特征,映射率88.41%。模型组较正常组筛得109个差异代谢物(63个上调、46个下调),富集于胆汁分泌、鞘脂代谢及甾体激素生物合成通路。低、中、高剂量组分别筛得75、61、55个差异代谢物,PC(16:0/20:5) 在三组均呈反向调节。WGCNA 识别5个模块,筛选出SM(d18:0/16:1)、氢化可的松、胆酸等候选关键代谢物。结论:消渴固肾方系统性重塑T2DM 大鼠血清代谢组,涉及胆汁酸、鞘脂代谢及甾体激素合成通路,为后续机制验证提供候选靶点。

Keywords
消渴固肾方
2 型糖尿病
非靶向代谢组学
胆汁酸
鞘脂代谢
WGCNA
References

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