首页|葱白提取物调控HIF-1α/VEGF通路抑制缺氧/复氧心肌细胞的氧化应激和凋亡

葱白提取物调控HIF-1α/VEGF通路抑制缺氧/复氧心肌细胞的氧化应激和凋亡

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目的:评估葱白提取物(fistular onion bulb,FOB)通过调控HIF-1α/VEGF通路对缺氧/复氧H9c2心肌细胞氧化应激和凋亡的影响。方法:基于H9c2大鼠心肌细胞构建H/R细胞模型,通过细胞形态观察和CCK-8法检测确定细胞复氧时间为24 h。将细胞分为 Control 组、H/R组、H/R+FOB 组、H/R+YC-1(HIF-1α抑制剂)组、H/R+YC-1+FOB 组。CCK-8 法检测各组细胞增殖活力,流式细胞术检测细胞凋亡及细胞中活性氧(ROS)含量,生化试剂盒检测细胞中丙二醛(MDA)、乳酸脱氢酶(LDH)含量,Western blot检测细胞中 Bax、Bcl-2、低氧诱导因子-1α(hypoxia-inducible factor-1α,HIF-1α)和血管内皮生长因子(vascular endothelial growth factor,VEGF)的蛋白表达水平。结果:与Control组比较,H/R组细胞增殖活力下降(P<0。05),凋亡率上升(P<0。05),ROS、MDA和LDH含量上升(P<0。05),凋亡相关蛋白Bax表达上升(P<0。05)、Bcl-2表达下降(P<0。05),HIF-1α/VEGF通路蛋白表达均上升(P<0。05)。与H/R组比较,H/R+FOB组和H/R+YC-1组细胞增殖活力增加(P<0。05),凋亡率下降(P<0。05),ROS、MDA和LDH含量下降(P<0。05),Bcl-2蛋白表达增加(P<0。05),Bax、HIF-1α、VEGF蛋白表达均下降(P<0。05)。与H/R+YC-1组比较,H/R+YC-1+FOB组变化趋势更显著。结论:FOB通过抑制HIF-1α/VEGF通路,从而抑制缺氧/复氧心肌细胞的氧化应激和凋亡,减轻细胞损伤。
Fistular onion bulb regulated HIF-1α/VEGF pathway for arresting oxidative stress and apoptosis of hypoxic/reoxygenated cardiomyocytes
OBJECTIVE To evaluate the effects of fistular onion bulb(FOB)extract on oxidative stress and apoptosis in hypoxia/reoxygenated H9c2 cardiomyocytes through regulating HIF-1α/VEGF pathway.METHODS Hypoxia/reoxygenation(H/R)cell model was constructed by H9c2 rat cardiomyocytes with a reoxygenation time of 24 h as determined by cell morphol-ogy observation and CCK-8 assay.The cells were assigned into five groups of control,H/R,H/R+FOB,H/R+YC-1(HIF-1α inhibitor)and H/R+YC-1+FOB.Cell proliferation activity was assessed by CCK-8 while cell apoptosis by flow cytometry.The contents of reactive oxygen species(ROS)were detected by flow cytometry and malondialdehyde(MDA)and level of lac-tate dehydrogenase(LDH)by biochemical kits.Westem blot was utilized for determining the protein expression levels of Bax,Bcl-2,hypoxia-inducible factor-1α(HIF-1α)and vascular endothelial growth factor(VEGF).RESULTS As compared with control group,cell proliferation activity and apoptotic rate decreased in H/R group(P<0.05)while the contents of ROS,MDA and LDH rose significantly(P<0.05).Additionally,apoptosis-related protein Bax was up-regulated(P<0.05)while Bcl-2 down-regulated(P<0.05).Protein expression levels of HIF-1α/VEGF pathway became elevated(P<0.05).As compared with H/R group,cell proliferation activity spiked obviously in both H/R+FOB and H/R+YC-1 groups(P<0.05)while apop-totic rate decreased(P<0.05).Furthermore,the contents of ROS,MDA and LDH all declined(P<0.05)while Bcl-2 protein was up-regulated(P<0.05).The protein expressions of Bax,HIF-1α and VEGF all decreased(P<0.05).CONCLUSION FOB may suppress the activation of HIF-1α/VEGF pathway,resulting in lower oxidative stress and slower apoptosis within hypoxic/reoxygenated cardiomyocytes,ultimately alleviating cellular injury.

myocardial infarctionfistular onion bulbhypoxia/reoxygenationoxidative stressapoptosisHIF-1α/VEGF pathway

吴勇宏、贺立群、潘婉、田立群、卜文玉、康棋棋、刘翰

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武汉市第一医院心血管内科,湖北武汉 430022

湖北中医药大学第一临床学院,湖北武汉 430070

心肌梗死 葱白提取物 缺氧/复氧 氧化应激 细胞凋亡 HIF-1α/VEGF通路

2024

中国医院药学杂志
中国药学会

中国医院药学杂志

CSTPCD北大核心
影响因子:1.198
ISSN:1001-5213
年,卷(期):2024.44(23)