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昆明医科大学第一附属医院临床药学中心,昆明 650032
药师,硕士研究生。研究方向:临床药学、药理学。E-mail:2079957968@qq.com
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
收稿日期:2024-07-30,
修回日期:2025-01-07,
录用日期:2025-01-21,
纸质出版日期:2025-03-30
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雷雨田,冯丹,陈新利,等.三七丹参片治疗非酒精性脂肪性肝病的作用机制研究[J].中国药房,2025,36(06):674-679.
LEI Yutian,FENG Dan,CHEN Xinli,et al.Effect and mechanism of Sanqi danshen tablets in the treatment of non-alcoholic fatty liver disease[J].ZHONGGUO YAOFANG,2025,36(06):674-679.
雷雨田,冯丹,陈新利,等.三七丹参片治疗非酒精性脂肪性肝病的作用机制研究[J].中国药房,2025,36(06):674-679. DOI: 10.6039/j.issn.1001-0408.2025.06.06.
LEI Yutian,FENG Dan,CHEN Xinli,et al.Effect and mechanism of Sanqi danshen tablets in the treatment of non-alcoholic fatty liver disease[J].ZHONGGUO YAOFANG,2025,36(06):674-679. DOI: 10.6039/j.issn.1001-0408.2025.06.06.
目的
2
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
2
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
2
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
2
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。
OBJECTIVE
2
To investigate the potential mechanism of Sanqi danshen tablets in the treatment of non-alcoholic fatty liver disease (NAFLD).
METHODS
2
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
2
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
2
Sanqi danshen tablets exert anti-inflammatory, antioxidant and lipid metabolism regulating effects by influencing the levels of inflammation, oxidative stress and lipids metabolism-related indicators, thereby improving NAFLD in rats.
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