天津医药 ›› 2025, Vol. 53 ›› Issue (8): 796-801.doi: 10.11958/20251272

• 细胞与分子生物学 • 上一篇    下一篇

秦皮甲素调节HMGB1/RAGE信号通路对缺氧/复氧诱导的心肌细胞损伤的影响

万艳波(), 刘明(), 王勇   

  1. 安阳市人民医院心血管内二科(邮编455000)
  • 收稿日期:2025-04-08 修回日期:2025-05-20 出版日期:2025-08-15 发布日期:2025-08-12
  • 通讯作者: E-mail:liuming815@126.com
  • 作者简介:万艳波(1982),男,副主任医师,主要从事冠心病诊治方面研究。E-mail:wanyanbo1982@163.com
  • 基金资助:
    河南省医学科技攻关计划项目(LHGJ20191271)

The effect of esculin on hypoxia/reoxygenation induced myocardial cell injury by regulating HMGB1/RAGE signaling pathway

WAN Yanbo(), LIU Ming(), WANG Yong   

  1. Department of the Second Cardiovascular Medicine, Anyang People's Hospital, Anyang 455000, China
  • Received:2025-04-08 Revised:2025-05-20 Published:2025-08-15 Online:2025-08-12
  • Contact: E-mail:liuming815@126.com

摘要:

目的 探讨秦皮甲素(ESCL)通过调节高迁移率族蛋白B1(HMGB1)/晚期糖基化终产物受体(RAGE)信号通路对缺氧/复氧(H/R)诱导的心肌细胞损伤的影响。方法 将H9c2细胞分为Control组,H/R组,ESCL-低、中、高浓度(ESCL-L、M、H,0.4、0.8、1.6 mmol/L)组,ESCL-H+pcDNA-NC组,ESCL-H+pcDNA-HMGB1组。Annexin V-FITC染色法检测H9c2细胞凋亡率;酶联免疫吸附试验检测白细胞介素(IL)-18、IL-1β、肿瘤坏死因子(TNF)-α和丙二醛(MDA)、乳酸脱氢酶(LDH)含量和超氧化物歧化酶(SOD)活性;DCHF-DA荧光探针检测活性氧(ROS)荧光强度;蛋白免疫印迹法检测B淋巴细胞瘤-2(Bcl-2)、Bcl-2相关X蛋白(Bax)、HMGB1、RAGE蛋白表达水平。结果 与Control组相比,H/R组H9c2细胞凋亡率、IL-18、IL-1β、TNF-α、MDA、LDH、ROS荧光强度、Bax、HMGB1和RAGE蛋白表达水平升高,Bcl-2蛋白表达水平、SOD活性降低(P<0.05);与H/R组相比,ESCL-L、M、H组细胞凋亡率、IL-18、IL-1β、TNF-α、MDA、LDH、ROS荧光强度、Bax、HMGB1和RAGE蛋白表达水平依次降低,Bcl-2蛋白表达水平、SOD活性依次升高(P<0.05);过表达HMGB1逆转了ESCL对H/R诱导的心肌细胞损伤的保护作用。结论 ESCL可能通过抑制HMGB1/RAGE通路减轻H/R诱导的心肌细胞损伤。

关键词: 肌细胞, 心脏, 秦皮甲素, HMGB1蛋白质, 高级糖化终产物受体, 细胞凋亡, 低氧, 复氧

Abstract:

Objective To explore the effect of esculin (ESCL) on hypoxia/reoxygenation (H/R)-induced myocardial cell injury by regulating high mobility group B1 (HMGB1)/receptor of advanced glycation endproducts (RAGE) signaling pathway. Methods H9c2 cells were divided into the control group, the H/R group, the ESCL-low group, the ESCL-medium group and the ESCL-high group (ESCL-L, M, H, 0.4, 0.8, 1.6 mmol/L), the ESCL-H+pcDNA-NC group and the ESCL-H+pcDNA-HMGB1 group. The AnnexinV FITC staining method was used to detect the apoptosis rate of H9c2 cells. Enzyme linked immunosorbent assay was used to measure interleukin (IL)-18, IL-1β, tumor necrosis factor (TNF)-α, the malondialdehyde (MDA), lactate dehydrogenase (LDH) contents and the superoxide dismutase (SOD) activity. The DCHF-DA fluorescent probe was performed to detect active oxygen (ROS) fluorescence intensity. Immunoblotting was performed to detect B-cell lymphoma-2 (Bcl-2), Bcl-2 associated X protein (Bax), HMGB1 and RAGE proteins. Results Compared with the control group,the H/R group showed conspicuously higher apoptosis rate, IL-18, IL-1β, TNF-α, MDA, LDH, ROS fluorescence intensity, Bax, HMGB1 and RAGE proteins in H9c2 cells, and conspicuously lower Bcl-2 protein and SOD activity (P<0.05). Compared with the H/R group, the ESCL-L, ESCL-M and ESCL-H groups showed a gradual decrease in cell apoptosis rate, IL-18, IL-1β, TNF-α, MDA, LDH and ROS fluorescence intensity, Bax, HMGB1 and RAGE proteins with increasing ESCL concentration, and a gradual increase in Bcl-2 protein and SOD activity (P<0.05). Overexpression of HMGB1 reversed the protective effect of ESCL on H/R induced cardiomyocyte injury. Conclusion ESCL may reduce H/R induced cardiomyocyte injury by inhibiting HMGB1/RAGE pathway.

Key words: myocytes, cardiac, aesculi, HMGB1 protein, receptor for advanced glycation end products, apoptosis, hypoxia, reoxygenation

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