天然产物研究与开发 ›› 2026, Vol. 38 ›› Issue (9): 1980-1987.doi: 10.16333/j.1001-6880.2026.9.012 cstr: 32307.14.1001-6880.2026.9.012

• 开发研究 • 上一篇    下一篇

麝香酮对H2 O2 诱导人脐静脉内皮细胞损伤的保护作用及机制研究

杜晨曦 1,魏乐乐 1,席俊丽 2,权赫秀 2,罗  云 1∗   

  1. 1江西中医药大学现代中药制剂教育部重点实验室;2 江西中医药大学中医学院,南昌330004

  • 出版日期:2026-09-24 发布日期:2026-09-22
  • 基金资助:

    国家自然科学基金(82160824)

Protective effect and mechanism of muscone on human umbilical vein endothelial cells induced by H2O2

DU Chen-xi1,WEI Le-le1,XI Jun-li2,QUAN He-xiu2,LUO Yun1∗   

  1. 1Key Laboratory of Modern Preparation of Traditional Chinese Medicine,Ministry of Education,Jiangxi University of Chinese Medicine; 2School of Chinese Medicine,Jiangxi University of Chinese Medicine,Nanchang 330004,China

  • Online:2026-09-24 Published:2026-09-22

摘要:

研究麝香酮对H2O2 诱导的人脐静脉内皮细胞(human umbilical vein endothelial cells,HUVECs)氧化损伤的保护作用及机制。采用MTS 法检测麝香酮对HUVECs 细胞增殖活性的影响;伊红染色法观察细胞形态变化;绿色荧光探针测定细胞内活性氧(reactive oxygen species,ROS)水平;超氧化物歧化酶(superoxide dismutase,SOD)、过氧化氢酶 (catalase,CAT)试剂盒检测HUVECs 细胞内抗氧化酶活力;流式细胞术检测细胞凋亡率;Western blot 分别检测剪切的半胱天冬酶-3(cleaved cysteine-aspartic protease 3,cleaved Caspase-3)、B 细胞淋巴瘤-2(B-cell lymphoma-2,BCL-2)及 B 细胞淋巴瘤2 相关X(BCL-2 associated X protein,BAX)蛋白的表达情况。结果显示麝香酮(0. 9 ~ 9 μg/ mL)对HUVECs 细胞生长无任何影响,H2O2 诱导HUVECs 细胞发生氧化损伤的最佳条件是400 μmol/ L 作用2 h,与H2O2 组比较,麝香酮(1. 125 ~ 4. 5 μg/ mL) 可以抑制H2O2 对HUVECs 细胞形态的改变,增加细胞成活率(P < 0. 001),提高 SOD 和CAT 活性(P < 0. 001,P < 0. 05),降低细胞凋亡率和ROS 水平(P < 0. 01,P < 0. 001),使BCL-2 蛋白表达升高 (P < 0. 01),Cleaved Caspase-3 和BAX 蛋白表达减少(P < 0. 01,P < 0. 01)。结果表明,麝香酮对H2O2 诱导的HUVECs 细胞损伤具有保护作用,作用机制可能与清除ROS、改善细胞内抗氧化酶活性、抑制细胞凋亡等有关。

关键词:

"> 麝香酮, 人脐静脉内皮细胞, 氧化应激, 细胞凋亡

Abstract:

This study aims to investigate the protective effect and mechanism of muscone on human umbilical vein endothelial cells (HUVECs) induced by H2O2. The impacts on HUVECs cell proliferation vitality were evaluated through MTS assay;The morphology of HUVECs was observed by eosin staining method;The intracellular reactive oxygen species(ROS) levels were detected by green fluorescent probes;Intracellular antioxidant enzyme activity in HUVECs was assessed by the superoxide dismutase (SOD) and catalase (CAT) kits;flow cytometry was used to detect cell apoptosis rate;Western blot was used to detect the expression of Cleaved Caspase-3,B-cell lymphoma-2(BCL-2),and BCL-2 associated X protein (BAX) proteins. The results indicated that muscone (0. 9-9. 0 μg/ mL) had no effect on the growth of HUVECs. The optimal concentration of H2O2 for inducing oxidative damage in HUVECs was 400 μmol/ L for 2 hours. Compared with the H2O2 group,muscone (1. 125-4. 5 μg/ mL) inhibited the morphological changes of HUVECs induced by H2O2. Cell morphology was improved,cell viability was increased(P < 0. 001),the activities of SOD and CAT were enhanced(P < 0. 001,P < 0. 05),and the apoptosis rate and ROS levels were decreased by muscone(P < 0. 01,P < 0. 001). Western blot showed that the protein expressions of BCL-2 in muscone group were higher(P < 0. 01),while the expressions of Cleaved Caspase-3 and BAX were lower than that in H2O2 group (P < 0. 01,P < 0. 01). These findings suggested that muscone exhibited a protective effect against H2O2-induced HUVECs damage,potentially through the mechanisms involving the clearance of ROS,improvement of intracellular antioxidant enzyme activity,and inhibition of apoptosis.

Key words:

"> muscone, human umbilical vein endothelial cells, oxidative stress, apoptosis

中图分类号: 

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