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恩格列净和沙库巴曲缬沙坦通过抑制心脏胚胎 H9c2 心肌细胞中的氧化应激和缺氧逆转甲氨蝶呤的心脏毒性 - 电镜下观察到的线粒体形态的作用。

Empagliflozin and sacubitril/valsartan reverse methotrexate cardiotoxicity by repressing oxidative stress and hypoxia in heart embryonic H9c2 cardiomyocytes - the role of morphology of mitochondria observed on electron microscopy.

机构信息

Department of Cardiology, Faculty of Medicine, Istanbul Atlas University, Istanbul, Turkey.

出版信息

Eur Rev Med Pharmacol Sci. 2023 May;27(9):3979-3992. doi: 10.26355/eurrev_202305_32304.

Abstract

OBJECTIVE

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.

MATERIALS AND METHODS

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).

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

材料和方法

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

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。

结论

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。

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