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三七丹参片治疗非酒精性脂肪性肝病的作用机制研究
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          雷雨田 ,冯 丹,陈新利,杨 媛,吴 晖(昆明医科大学第一附属医院临床药学中心,昆明 650032)
          中图分类号  R965;R285.5      文献标志码  A      文章编号  1001-0408(2025)06-0674-06
          DOI  10.6039/j.issn.1001-0408.2025.06.06

          摘   要  目的  探讨三七丹参片治疗非酒精性脂肪性肝病(NAFLD)的潜在机制。方法  采用网络药理学方法,挖掘三七丹参片治
          疗NAFLD的核心靶点,并进行基因本体(GO)功能及京都基因和基因组数据库(KEGG)通路富集分析。基于网络药理学结果,以
          SD大鼠为对象,以高脂饲料喂养构建NAFLD模型,考察三七丹参片对NAFLD大鼠肝组织脂滴空泡、脂质蓄积等病理改变以及脂
          质代谢、炎症反应、氧化应激指标的影响。结果  共筛选出三七丹参片治疗NAFLD的核心靶点20个,主要涉及生物调节、细胞膜、
          结合等GO功能,并富集于炎症反应、氧化应激、脂质代谢相关信号通路。动物实验显示,与模型组相比,三七丹参片低、中、高剂
          量组和阳性对照药(辛伐他汀)组大鼠肝组织内脂滴空泡明显减少,脂滴数量明显减少且颜色变浅;其肝组织中总胆固醇、甘油三
          酯(三七丹参片中剂量组除外)、天冬氨酸转氨酶、丙氨酸转氨酶、肿瘤坏死因子α(三七丹参片低剂量组除外)、白细胞介素17(三
          七丹参片各剂量组除外)、丙二醛(三七丹参片低剂量组除外)含量均显著降低,超氧化物歧化酶含量均显著升高(P<0.01或P<
          0.05)。结论  三七丹参片可通过影响炎症反应、氧化应激、脂质代谢等相关指标含量来发挥抗炎、抗氧化、调节脂质代谢的作用,
          从而改善大鼠的NAFLD。
          关键词  三七丹参片;非酒精性脂肪性肝病;炎症反应;氧化应激;脂质代谢


          Effect and mechanism of Sanqi danshen tablets in the treatment of non-alcoholic fatty liver disease
          LEI Yutian,FENG Dan,CHEN Xinli,YANG Yuan,WU Hui(Dept.  of  Clinical  Pharmacy  Center,  the  First
          Affiliated Hospital of Kunming Medical University, Kunming 650032, China)

          ABSTRACT    OBJECTIVE  To  investigate  the  potential  mechanism  of  Sanqi  danshen  tablets  in  the  treatment  of  non-alcoholic
          fatty  liver  disease (NAFLD).  METHODS  Core  targets  of  Sanqi  danshen  tablets  in  the  treatment  of  NAFLD  were  explored  by
          network  pharmacological  methods.  Gene  ontology (GO)  functional  enrichment  analysis  and  Kyoto  Encyclopedia  of  Genes  and
          Genomes (KEGG) pathway enrichment analysis were also performed. Based on the results obtained from network pharmacological
          studies,  using  SD  rats  as  subjects,  the  NAFLD  model  was  induced  by  feeding  them  high-fat  diet.  The  effects  of  Sanqi  danshen
          tablets on pathological changes such as lipid droplet vacuoles and lipid accumulation in the liver tissue of NAFLD rats, as well as
          its impact on relative indicators of lipid metabolism, inflammatory responses and oxidative stress, were investigated. RESULTS A
          total of 20 core targets for the treatment of NAFLD with Sanqi danshen tablets were screened, primarily involved in GO functions
          such  as  biological  regulation,  cellular  membrane  and  binding,  and  enriched  in  signaling  pathways  related  to  inflammatory
          responses, oxidative stress and lipid metabolism. Compared with the model group, lipid droplet vacuoles were reduced significantly
          in  low-dose,  medium-dose,  high-dose  groups  of  Sanqi  danshen  tablets  and  positive  control (simvastatin)  group,  the  number  of
          lipid droplets decreased significantly and the color became lighter. The contents of total cholesterol, triglyceride (except for medium-
          dose  group  of  Sanqi  danshen  tablets),  aspartate  transaminase,  alanine  transaminase,  tumor  necrosis  factor-α (except  for  low-dose
          group  of  Sanqi  danshen  tablets),  interleukin-17 (except  for  Sanqi  danshen  tablets  groups)  and  malondialdehyde (except  for  low-
          dose  group  of  Sanqi  danshen  tablets)  in  liver  tissue  were  significantly  decreased,  while  the  content  of  superoxide  dismutase  was
          significantly  increased (P<0.01  or  P<0.05).  CONCLUSIONS  Sanqi  danshen  tablets  exert  anti-inflammatory,  antioxidant  and
                                                              lipid  metabolism  regulating  effects  by  influencing  the  levels  of
              Δ 基金项目 云南省科技厅科技计划项目基础研究专项(No.
          202301AT070152);云南省科技厅科技计划项目重大科技专项(生物医              inflammation,  oxidative  stress  and  lipids  metabolism-related
          药)(No.2019ZF005);中华国际医学交流基金会-中华医学会临床药学              indicators, thereby improving NAFLD in rats.
          分会临床药学科研基金项目(No.Z-202146-2101-2023)                 KEYWORDS    Sanqi  danshen  tablets;  non-alcoholic  fatty
             *第一作者 药师,硕士研究生。研究方向:临床药学、药理学。E-
                                                              liver  disease;  inflammatory  response;  oxidative  stress;  lipid
          mail:2079957968@qq.com
                                                              metabolism
              # 通信作者 主任药师,博士生导师,硕士。研究方向:临床药学、
          药理学。E-mail:kyz-ggyx@163.com


          · 674 ·    China Pharmacy  2025 Vol. 36  No. 6                               中国药房  2025年第36卷第6期
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