Department of Cardiology, Faculty of Medicine, Istanbul Atlas University, Istanbul, Turkey.
Eur Rev Med Pharmacol Sci. 2023 May;27(9):3979-3992. doi: 10.26355/eurrev_202305_32304.
Oxidative stress and hypoxia play an important role in the pathogenesis of various cardiovascular diseases. We aimed to evaluate the effectiveness of sacubitril/valsartan (S/V) and Empagliflozin (EMPA) on hypoxia-inducible factor-1α (HIF-1α) and oxidative stress in H9c2 rat embryonic cardiomyocyte cells.
BH9c2 cardiomyocyte cells were treated with methotrexate (MTX) (10-0.156 μM), empagliflozin (EMPA; 10-0.153 µM) and sacubitril/valsartan (S/V; 100-1.062 µM) for 24, 48 and 72 h. The half maximum inhibitory concentration (IC50) and half maximum excitation concentration (EC50) values of MTX, EMPA and S/V were determined. The cells under investigation were exposed to 2.2 μM MTX before treatment with 2 μM EMPA and 25 μM S/V. The cell viability, lipid peroxidation, oxidation of proteins and antioxidant parameters were measured while morphological changes were also observed by transmission electron microscopy (TEM).
The results showed that treatment with 2 µM EMPA, 25 µM S/V or their combination produced a protective effect against the reduction in cell viability caused by 2.2 µM MTX. While HIF-1α levels plunged to their lowest with S/V treatment, oxidant parameters dipped, and antioxidant parameters soared to their highest level with S/V and EMPA combination treatment. A negative correlation was found between HIF-1α and total antioxidant capacity in the S/V treatment group.
A significant decrease in HIF-1α and oxidant molecules together with an enhancement in antioxidant molecules and normalization of the mitochondria morphology as observed on electron microscopy in S/V and EMPA-treated cells were detected. Although S/V and EMPA have both protective effects against cardiac ischemia and oxidative damage, this effect may be increased more with S/V treatment alone compared to combined treatment.
氧化应激和缺氧在各种心血管疾病的发病机制中起着重要作用。我们旨在评估沙库巴曲缬沙坦(S/V)和恩格列净(EMPA)对 H9c2 大鼠胚胎心肌细胞中缺氧诱导因子-1α(HIF-1α)和氧化应激的疗效。
用甲氨蝶呤(MTX)(10-0.156 μM)、恩格列净(EMPA;10-0.153 µM)和沙库巴曲缬沙坦(S/V;100-1.062 µM)处理 BH9c2 心肌细胞 24、48 和 72 小时。测定 MTX、EMPA 和 S/V 的半最大抑制浓度(IC50)和半最大激发浓度(EC50)值。在先用 2 μM EMPA 和 25 μM S/V 处理之前,将这些细胞暴露于 2.2 μM MTX 下。测量细胞活力、脂质过氧化、蛋白质氧化和抗氧化参数,同时通过透射电子显微镜(TEM)观察形态变化。
结果表明,用 2 μM EMPA、25 μM S/V 或它们的组合处理对 2.2 μM MTX 引起的细胞活力降低具有保护作用。S/V 处理时 HIF-1α 水平降至最低,氧化剂参数下降,S/V 和 EMPA 联合处理时抗氧化参数升至最高。S/V 治疗组中发现 HIF-1α 与总抗氧化能力呈负相关。
在 S/V 和 EMPA 处理的细胞中,观察到 HIF-1α 和氧化剂分子显著减少,抗氧化分子增加,线粒体形态正常化,这些变化在电镜下可见。尽管 S/V 和 EMPA 都对心脏缺血和氧化损伤具有保护作用,但与联合治疗相比,单独使用 S/V 治疗可能会增加这种作用。