Safflor yellow A protects vascular endothelial cells from ox-LDL-mediated damage.

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Receptors and Signal Transduction Pub Date : 2022-02-01 Epub Date: 2020-11-09 DOI:10.1080/10799893.2020.1843492
Hu Zhang, Li-Juan Fan, Jun Liu, Jia-Qi Zhu, Ting-Ting Tan, Ming Li, You-Li Zhou
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引用次数: 3

Abstract

Atherosclerosis is a chronic disease of arteries, which constitutes the pathological basis of a series of cardiovascular diseases. The inflammatory response of vascular endothelial cells mediated by oxidized low density lipoprotein (ox-LDL) is the early behavior and main signal of atherosclerosis. In this study, the damage model of vascular endothelial cells treated with ox-LDL was used to reproduce the damage process of vascular endothelial cells in the process of atherosclerosis. Cell viability was detected by CCK-8. The release levels of reactive oxygen species, nitric oxide, and superoxide dismutase (SOD) were detected by commercial kits. EdU cell proliferation assay was used to detect cell proliferation, real-time fluorescent quantitative PCR and Western blot were used to detect the expression level of related genes. The results showed we successfully constructed a vascular endothelial injury model by incubating vascular endothelial cells with gradient concentrations of ox-LDL. The incubation of safflor yellow A (SYA) partially restored the loss of viability of vascular endothelial cells mediated by ox-LDL, and SYA could promote the proliferation of injured vascular endothelial cells. In addition, SYA may transmit related signals through the AMPK pathway to protect vascular endothelial cells from ox-LDL-mediated damage. All these results provide a further understanding of the occurrence and development of atherosclerosis, provide a theoretical basis for the use of SYA-related drugs in the treatment of cardiovascular diseases, and provide a reference paradigm for studying the pharmacology, toxicology, and mechanism of action of key active substances in TCM.

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红花黄A保护血管内皮细胞免受ox- ldl介导的损伤。
动脉粥样硬化是动脉的慢性疾病,是一系列心血管疾病的病理基础。氧化低密度脂蛋白(ox-LDL)介导的血管内皮细胞炎症反应是动脉粥样硬化的早期行为和主要信号。本研究采用ox-LDL处理血管内皮细胞损伤模型,再现动脉粥样硬化过程中血管内皮细胞的损伤过程。CCK-8检测细胞活力。用商业试剂盒检测活性氧、一氧化氮和超氧化物歧化酶(SOD)的释放水平。采用EdU细胞增殖法检测细胞增殖情况,采用实时荧光定量PCR和Western blot检测相关基因的表达水平。结果表明,我们用梯度浓度ox-LDL培养血管内皮细胞,成功构建了血管内皮损伤模型。红花黄A (SYA)孵育可部分恢复ox-LDL介导的血管内皮细胞活力丧失,并能促进损伤血管内皮细胞的增殖。此外,SYA可能通过AMPK通路传递相关信号,保护血管内皮细胞免受ox- ldl介导的损伤。这些结果为进一步认识动脉粥样硬化的发生发展提供了依据,为sya相关药物在心血管疾病治疗中的应用提供了理论依据,并为研究中医关键活性物质的药理学、毒理学和作用机制提供了参考范式。
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来源期刊
Journal of Receptors and Signal Transduction
Journal of Receptors and Signal Transduction 生物-生化与分子生物学
CiteScore
6.60
自引率
0.00%
发文量
19
审稿时长
>12 weeks
期刊介绍: Journal of Receptors and Signal Tranduction is included in the following abstracting and indexing services: BIOBASE; Biochemistry and Biophysics Citation Index; Biological Abstracts; BIOSIS Full Coverage Shared; BIOSIS Previews; Biotechnology Abstracts; Current Contents/Life Sciences; Derwent Chimera; Derwent Drug File; EMBASE; EMBIOLOGY; Journal Citation Reports/ Science Edition; PubMed/MedLine; Science Citation Index; SciSearch; SCOPUS; SIIC.
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