中国药物警戒 ›› 2026, Vol. 23 ›› Issue (3): 259-266.
DOI: 10.19803/j.1672-8629.20250941

• 基础与临床研究 • 上一篇    下一篇

康体瘦身方透皮成分及其干预肥胖症作用机制研究

孙健1, 杨司宇1,2△, 米玛卓嘎3, 仁增3, 边巴顿珠3, 王榆鑫1, 程浩洁1, 次仁3#, 樊新荣1,*   

  1. 1中国中医科学院医学实验中心,北京 100700;
    2黑龙江中医药大学研究生院,黑龙江 哈尔滨 150006;
    3西藏自治区藏医院,西藏自治区藏医药研究院,西藏 拉萨 850000
  • 收稿日期:2025-12-29 出版日期:2026-03-15 发布日期:2026-03-17
  • 通讯作者: *樊新荣,男,博士,主任医师·博导,代谢疾病调治研究。E-mail: fxr1973@126.com。#为共同通信作者。
  • 作者简介:孙健,男,博士,研究员,中药物质基础与活性机制研究。Δ为并列第一作者。
  • 基金资助:
    国家自然科学基金资助项目(T2341017); 国家中医药管理局科技项目(GZY-KJS-2023-049); 西藏自治区藏医药管理局局级科研课题及标准化研究项目(JJKT2023001)

Transdermally Absorbed Components of Kangti Shoushen Formula and Their Mechanisms against Obesity

SUN Jian1, YANG Siyu1,2△, MIMA Zhuoga3, REN Zeng3, BIANBA Dunzhu3, WANG Yuxin1, CHENG Haojie1, CI Ren3#, FAN Xinrong1,*   

  1. 1Medical Experimental Center, China Academy of Chinese Medical Sciences, Beijing 100700, China;
    2Graduate School, Heilongjiang University of Chinese Medicine, Harbin Heilongjiang 150006, China;
    3Tibetan Hospital of Tibet Autonomous Region (Tibet Autonomous Region Institute of Tibetan Medicine), Lhasa Xizang 850000, China
  • Received:2025-12-29 Online:2026-03-15 Published:2026-03-17

摘要: 目的 探讨康体瘦身方治疗肥胖症的潜在活性成分及作用机制。方法 采用高效液相色谱-四极杆飞行时间质谱联用技术(HPLC-Q-TOF-MS/MS)分析康体瘦身方药浴透皮实验后的透皮成分,使用PharmMapper和GeneCards等数据库筛选康体瘦身方关联靶点与肥胖相关靶点,并通过Venny筛选康体瘦身方治疗肥胖症的潜在靶点;应用String数据库与Cytoscape软件构建并分析蛋白质-蛋白质相互作用(PPI)网络,筛选核心靶点;通过基因本体(GO)和京都基因与基因组百科全书(KEGG)进行富集分析。结果 共检测出21个康体瘦身方透皮成分,获得509个药物潜在靶点、1 549个肥胖症治疗潜在靶点和176个交集靶点,筛选出65个核心靶点。经网络药理学GO和KEGG富集分析,发现康体瘦身方可能通过异氨己酸(L-Norleucine)、缬氨酸(Valine)、阿魏酸(Ferulic Acid)等多成分调控AKT1TNFPPARγESR1等多靶点,进而调节HIF-1、ROS、THR等信号通路发挥治疗肥胖症的作用。结论 康体瘦身方可能通过维持糖脂代谢稳态、减轻炎症反应与氧化应激、参与食欲抑制过程,发挥其治疗肥胖的作用机制。本研究体现藏药复方“多成分、多靶点、多途径”的治疗优势,为康体瘦身方临床合理应用提供参考。

关键词: 康体瘦身方, 肥胖症, 透皮成分, 高效液相色谱-四极杆-飞行时间串联质谱, 作用机制

Abstract: Objective To study the potential transdermal active components and underlying mechanisms of Kangti Shoushen Formula (KTSF) in the treatment of obesity. Methods The transdermal components of KTSF after experimental permeation were analyzed using HPLC-Q-TOF-MS/MS. Potential targets of KTSF and obesity-related targets were obtained from the PharmMapper and GeneCards databases while the intersecting targets were identified with Venny. The STRING database and Cytoscape software were used to construct and analyze protein-protein interaction (PPI) networks and screen core targets. Finally, enrichment analysis was conducted using Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG). Results A total of 21 transdermal components of KTSF were detected. In total, 509 putative KTSF targets and 1,549 obesity-associated targets were identified, yielding 176 overlapping targets. Subsequently, 65 core targets were prioritized. GO and KEGG enrichment analyses suggested that the anti-obesity effects of KTSF might be mediated by multiple components, including L-norleucine, valine, and ferulic acid, which acted on key targets such as AKT1, TNF, PPARγ, and ESR1, thereby modulating pathways related to HIF-1, reactive oxygen species (ROS), and thyroid hormone receptor (THR) signaling. Conclusion KTSF may deliver therapeutic effect against obesity by maintaining glucose and lipid metabolic homeostasis, alleviating inflammatory responses and oxidative stress, and participating in appetite suppression. This study reveals the therapeutic advantages of this Tibetan herbal compound in terms of its “multi-component, multi-target, multi-pathway” characteristics, providing a reference for rational clinical applications of KTSF.

Key words: Kangti Shoushen Formula, Obesity, Transdermal Components, HPLC-Q-TOF-MS/MS, Mechanism

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