Suppr超能文献

没食子酸通过激活 Nrf2 并抑制 NF-[Formula: see text]B 通路减轻心肌缺血再灌注损伤诱导的氧化应激。

Maslinic Acid Ameliorates Myocardial Ischemia Reperfusion Injury-Induced Oxidative Stress via Activating Nrf2 and Inhibiting NF-[Formula: see text]B Pathways.

机构信息

School of Medicine, Nankai University, Tianjin 300071, P. R. China.

Department of Cardiology, Tianjin First Center Hospital, Tianjin 300192, P. R. China.

出版信息

Am J Chin Med. 2023;51(4):929-951. doi: 10.1142/S0192415X2350043X. Epub 2023 Mar 27.

Abstract

Maslinic acid (MA) is a pentacyclic triterpene obtained from the peel of olives that exhibits anti-inflammatory and antioxidant properties in several conditions. Our previous study revealed that MA exerted a cardioprotective effect by repressing inflammation and apoptosis during myocardial ischemia-reperfusion injury (MIRI). However, data regarding the antioxidative effects of MA on MIRI remains limited. This study aims to elucidate the antioxidative roles and underlying mechanisms of MA on MIRI. The left anterior descending coronary artery of rats was subjected to ligate for the induction of the ischemia/reperfusion (I/R) model and the H9c2 cells were exposed to hydrogen peroxide (HO) to mimic oxidative stress. The results showed that MA reduced the I/R-induced myocardial injury and HO-induced cardiomyocyte death in a dose-dependent manner. Meanwhile, MA increased the activities of glutathione and superoxide dismutase both and while lowering the levels of reactive oxygen species and malondialdehyde. Mechanistically, MA could facilitate Nrf2 nuclear translocation, activate the Nrf2/HO-1 signaling pathway, and repress the NF-[Formula: see text]B signaling pathway both in I/R- and HO-induced oxidative stress. Besides, MA promoted the intranuclear Nrf2 and HO-1 expression, which could in part be improved by QNZ (NF-[Formula: see text]B inhibitor) in HO-insulted cells. Conversely, MA markedly reduced the intranuclear NF-[Formula: see text]B p65 and TNF-[Formula: see text] expression, which could be partially abolished by ML385 (Nrf2 inhibitor). Overall, our results indicate that MA, in a dose-dependent manner, mitigated I/R-induced myocardial injury and oxidative stress via activating the Nrf2/HO-1 pathway and inhibiting NF-[Formula: see text]B activation. Furthermore, MA exerts its cardioprotective effect through regulating the crosstalk between the Nrf2 and NF-[Formula: see text]B pathways.

摘要

马尿酸(MA)是一种五环三萜,从橄榄皮中提取,在多种情况下具有抗炎和抗氧化特性。我们之前的研究表明,马尿酸通过抑制心肌缺血再灌注损伤(MIRI)期间的炎症和细胞凋亡发挥心脏保护作用。然而,关于马尿酸对 MIRI 的抗氧化作用的数据仍然有限。本研究旨在阐明 MA 对 MIRI 的抗氧化作用及其潜在机制。结扎大鼠左前降支冠状动脉诱导缺血/再灌注(I/R)模型,用过氧化氢(HO)处理 H9c2 细胞模拟氧化应激。结果表明,马尿酸呈剂量依赖性地减轻 I/R 诱导的心肌损伤和 HO 诱导的心肌细胞死亡。同时,马尿酸增加了谷胱甘肽和超氧化物歧化酶的活性,同时降低了活性氧和丙二醛的水平。在机制上,马尿酸可以促进 Nrf2 核转位,激活 Nrf2/HO-1 信号通路,并抑制 NF-κB 信号通路,无论是在 I/R 诱导的氧化应激还是 HO 诱导的氧化应激中。此外,马尿酸促进了核内 Nrf2 和 HO-1 的表达,在 HO 损伤的细胞中,用 QNZ(NF-κB 抑制剂)部分改善了这种表达。相反,马尿酸显著降低了核内 NF-κB p65 和 TNF-α的表达,用 ML385(Nrf2 抑制剂)部分消除了这种表达。总的来说,我们的结果表明,马尿酸以剂量依赖的方式通过激活 Nrf2/HO-1 通路和抑制 NF-κB 激活来减轻 I/R 诱导的心肌损伤和氧化应激。此外,马尿酸通过调节 Nrf2 和 NF-κB 通路之间的串扰发挥其心脏保护作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验