徐瑞豪, 樊慧, 张莉, 王慧慧, 仝瑶, 陈晶玉, 常高萍, 冯卫生, 郑晓珂. 怀菊花中咖啡酰基奎宁酸类化合物通过调节ERK/MAPK信号通路改善LPS诱导的HUVEC血管内皮细胞损伤J. 药学学报, 2019,54(7): 1207-1213. doi: 10.16438/j.0513-4870.2018-1060
引用本文: 徐瑞豪, 樊慧, 张莉, 王慧慧, 仝瑶, 陈晶玉, 常高萍, 冯卫生, 郑晓珂. 怀菊花中咖啡酰基奎宁酸类化合物通过调节ERK/MAPK信号通路改善LPS诱导的HUVEC血管内皮细胞损伤J. 药学学报, 2019,54(7): 1207-1213. doi: 10.16438/j.0513-4870.2018-1060
XU Rui-hao, FAN Hui, ZHANG Li, WANG Hui-hui, TONG Yao, CHEN Jing-yu, CHANG Gao-ping, FENG Wei-sheng, ZHENG Xiao-ke. Caffeoyl quinic acids in Chrysanthemum morifolium improve LPS-induced HUVEC vascular endothelial cell injury by regulating ERK/MAPK signaling pathwayJ. Acta Pharmaceutica Sinica, 2019,54(7): 1207-1213. doi: 10.16438/j.0513-4870.2018-1060
Citation: XU Rui-hao, FAN Hui, ZHANG Li, WANG Hui-hui, TONG Yao, CHEN Jing-yu, CHANG Gao-ping, FENG Wei-sheng, ZHENG Xiao-ke. Caffeoyl quinic acids in Chrysanthemum morifolium improve LPS-induced HUVEC vascular endothelial cell injury by regulating ERK/MAPK signaling pathwayJ. Acta Pharmaceutica Sinica, 2019,54(7): 1207-1213. doi: 10.16438/j.0513-4870.2018-1060

怀菊花中咖啡酰基奎宁酸类化合物通过调节ERK/MAPK信号通路改善LPS诱导的HUVEC血管内皮细胞损伤

Caffeoyl quinic acids in Chrysanthemum morifolium improve LPS-induced HUVEC vascular endothelial cell injury by regulating ERK/MAPK signaling pathway

  • 摘要: 初步研究怀菊花总提物对脂多糖(lipopolysaccharide,LPS)诱导的急性肺损伤小鼠模型的影响,并进一步探究从怀菊花中分离得到的3种咖啡酰基奎宁酸类化合物对血管内皮细胞损伤模型的干预作用及其机制。本文所有动物实验饲养及操作严格遵守国家动物福利伦理与保护相关规定。采用鼻腔滴注LPS的方法建立急性肺损伤小鼠模型,经菊花总提物灌胃给药6天后,检测小鼠肺湿重/干重比及小鼠肺泡灌洗液中肿瘤坏死因子-α(tumour necrosis factor-α,TNF-α)、白介素-6(interleukin-6,IL-6)、白介素-1β(interleukin-1β,IL-1β);使用人脐静脉内皮细胞(human umbilical vein endothelial cells,HUVEC)饥饿处理12 h后,以2.5 μg·mL-1 LPS诱导24 h建立血管内皮细胞损伤模型,经菊花中提取到的3种咖啡酰基奎宁酸类化合物处理24 h后,采用ELISA法测定细胞培养上清液中TNF-α、IL-6、IL-1β、血管细胞黏附分子-1(vascular cell adhesion molecule-1,VCAM-1)、内皮素-1(endothelin-1,ET-1)水平,TBA法检测丙二醛(malondialdehyde,MDA)水平,羟胺法检测超氧化物歧化酶(superoxide dismutase,SOD)水平,一步法检测一氧化氮(nitric oxide,NO)水平,Western blot法检测细胞内丝裂原活化蛋白激酶(mitogen-activated protein kinase,MAPK)信号通路p-MEK1/2、MEK1/2、p-ERK1/2、ERK1/2、p-JNK、JNK、p-P38、P38蛋白表达。结果显示,怀菊花总提物可显著降低小鼠肺湿重/干重比,降低肺泡灌洗液TNF-α、IL-6、IL-1β水平;怀菊花中咖啡酰基奎宁酸类化合物可显著升高SOD、NO水平,降低TNF-α、IL-6、IL-1β、VCAM-1、ET-1、MDA水平,并显著下调p-MEK1/2、p-ERK1/2的表达。综上,怀菊花总提物对急性肺损伤小鼠具有一定的保护作用,怀菊花中咖啡酰基奎宁酸类化合物可能是通过调节ERK/MAPK信号通路,抑制炎症因子、调节氧化应激水平,以及调节细胞间黏附分子和血管舒缩因子,从而改善LPS诱导的血管内皮细胞损伤。

     

    Abstract: To explore the effect of total extract of Chrysanthemum morifolium on lipopolysaccharide (LPS)-induced acute lung injury in mice, we studied the effects of three caffeoyl quinic acids isolated from Chrysanthemum morifolium on vascular endothelial cell injury and their mechanisms of action. All animal experiments were carried out strictly in accordance with the National Animal Welfare Ethics and Protection Regulations. A mouse model of acute lung injury was established by intranasal instillation of LPS. After 6 days of oral administration of chrysanthemum extract, the lung wet weight/dry weight ratio, tumour necrosis factor-α (TNF-α), interleukin-6 (IL-6), and interleukin-1β (IL-1β) were measured in mouse bronchoalveolar lavage fluid. Human umbilical vein endothelial cells (HUVEC) were serum starved for 12 h and treated with 2.5 μg·mL-1 LPS for 24 h to establish the in vitro model of vascular endothelial cell injury. After 24 h of treatment of caffeoyl quinic acids from Chrysanthemum morifolium, the levels of TNF-α, IL-6, IL-1β, vascular cell adhesion molecule-1 (VCAM-1) and endothelin-1 (ET-1) were measured by ELISA in the cell culture supernatant, the malondialdehyde (MDA) level was detected by TBA method, the superoxide dismutase (SOD) level was determined by hydroxylamine method, and the nitric oxide (NO) level was assayed by a one-step method. The levels of p-MEK1/2, MEK1/2, p-ERK1/2, ERK1/2, p-JNK, JNK, p-P38 and P38 of mitogen-activated protein kinase (MAPK) signaling pathway were detected by Western blot. The total extract of Chrysanthemum morifolium can significantly reduce the wet weight/dry weight ratio of lung in mice and the levels of TNF-α, IL-6 and IL-1β in alveolar lavage fluid. The caffeoyl quinic acids from Chrysanthemum morifolium significantly increased the levels of SOD and NO, decreased the levels of TNF-α, IL-6, IL-1β, VCAM-1, ET-1 and MDA, and significantly reduced the levels of p-MEK1/2, p-ERK1/2. In conclusion, total extracts of Chrysanthemum morifolium exhibit certain protective effect on mice with acute lung injury, and three caffeoyl quinic acids from Chrysanthemum morifolium may improve LPS-induced vascular endothelial cell injury by inhibiting inflammatory cytokines and oxidative stress, and regulating inter-cellular adhesion molecule and vasomotor factors through ERK/MAPK signaling pathway.

     

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