Ilex Pubescens 通过抑制 ROS/NLRP3 通路抑制心肌梗死后的脓毒症

Ting-fang Chen , Xiao-yu Jue , Jun-bang Chen , Bo Deng , Ke-feng Zeng , Si Chen , Zhang-bin Tan , Yong-zhen Tan , Bin Liu , Jing-zhi Zhang , Shuang-wei Zhang
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引用次数: 0

摘要

导言 蒲公英(IPES)是一种广泛用于治疗心血管疾病的传统中草药,在心肌梗塞中显示出潜在的抗炎能力。活性氧(ROS)和 NOD 样受体蛋白 3(NLRP3)通路是导致心脏病无菌性炎症的重要因素。本研究旨在阐明 IPES 抑制心肌梗死后脓毒血症的主要机制。方法通过结扎 C57BL/6 小鼠的左冠状动脉,建立心肌梗死模型并在体内进行实验。为了在体外建立热休克,从 Sprague-Dawley 大鼠心脏中提取了原代新生心肌细胞,并对其进行了缺氧-缺糖处理。通过腺病毒过表达 ROS 清除剂、NLRP3 抑制剂和 NLRP3,证实 IPES 可通过 ROS/NLRP3 途径抑制心肌脓毒症。此外,IPES 治疗还能明显抑制 ROS 的产生,降低 NLRP3 及其下游热蛋白相关蛋白的表达水平。在体外,IPES疗法在氧-葡萄糖剥夺/再氧合(OGD/R)细胞模型中以浓度依赖性的方式明显减少了细胞损伤和裂解。此外,IPES 还能与 ROS 清除剂 NAC 协同保护心肌细胞,而其对热蛋白沉积的抑制作用与 NLRP3 抑制剂并无明显差异。更重要的是,NLRP3 过表达可部分逆转 IPES 对热蛋白沉积的抑制作用。这些结果表明,IPES 通过抑制 ROS/NLRP3 通路抑制了心肌梗死后的热凋亡,为其在治疗心肌梗死中的潜在应用提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ilex pubescens inhibits pyroptosis post-myocardial infarction through suppression of the ROS/NLRP3 pathway

Ilex pubescens inhibits pyroptosis post-myocardial infarction through suppression of the ROS/NLRP3 pathway

Introduction

Ilex pubescens (IPES), a traditional Chinese herb widely used in cardiovascular diseases, has shown potential anti-inflammatory capabilities in myocardial infarction. Reactive Oxygen Species (ROS) and the NOD-like Receptor Protein 3 (NLRP3) pathway are significant contributors to aseptic inflammation in heart diseases. This study aims to elucidate the primary mechanism by which IPES inhibits pyroptosis post-myocardial infarction.

Methods

By ligating the left coronary artery in C57BL/6 mice, a myocardial infarction model was established to be conducted in vivo. To establish pyroptosis in vitro, primary neonatal cardiomyocytes, extracted from the hearts of Sprague-Dawley rats, were treated in an oxygen-glucose deprivation way. ROS scavenger, NLRP3 inhibitor, and NLRP3 was overexpressed by adenovirus to confirm IPES inhibiting myocardial pyroptosis through the ROS/NLRP3 pathway.

Results

In vivo, IPES exerted significant cardioprotective effects, as evidenced by reducing heart injury, improving cardiac function, and decreasing serum markers of cardiac damage. Furthermore, IPES treatment significantly inhibits ROS generation and reduces the expression levels of NLRP3 and its downstream pyroptosis-related proteins. In vitro, IPES therapy significantly decreased cell damage and pyroptosis in a concentration-dependent manner in an oxygen-glucose deprivation/re-oxygenation (OGD/R) cell model. Additionally, IPES demonstrates synergistic cardiomyocyte protection with the ROS scavenger NAC, whereas its inhibition of pyroptosis is not significantly different from that of the NLRP3 inhibitor. More importantly, the inhibitory impacts of IPES on pyroptosis were partially reversed by NLRP3 overexpression. The active components of IPES exhibit the ability to stably and efficiently bind with NLRP3.

Discussion

These results demonstrate that IPES inhibit pyroptosis post-MI by suppressing the ROS/NLRP3 pathway, providing a new insight into its potential application in treating MI.

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