在实验性心肌梗死模型中,L-精氨酸预干预可通过调节 OTULIN 水平和线粒体动力学发挥心脏保护作用。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2023-11-01 Epub Date: 2023-08-29 DOI:10.1007/s12192-023-01373-6
Sercan Kaya, Tuba Yalcın
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引用次数: 0

摘要

异丙肾上腺素(ISO)诱发的实验性心肌梗塞(MI)模型因其与人类心肌梗塞诱发的损伤相似而经常成为研究的首选。许多研究表明,L-精氨酸(L-Arg)这种半必需氨基酸对心血管疾病有益。本研究旨在确定 L-Arg 预先干预是否对实验性心肌梗死模型中的心脏组织具有保护作用。研究中使用的 28 只大鼠被随机分为 4 组:对照组、L-Arg 组、ISO 组和 L-Arg+ISO 组。在完成所有应用后,对血清中的心脏标记物和心脏组织进行生化、组织病理学和免疫组化检查。实验性心肌梗死模型的心脏标志物、组织病理学变化、氧化应激、炎症和细胞凋亡均有所增加。此外,服用 ISO 会降低心脏组织中的 OTULIN 水平和线粒体动力学。然而,在 ISO 诱导的心肌梗死中,L-Arg 的预先干预显示出显著的保护作用。补充具有心脏保护作用的 L-Arg 可降低心肌梗死中可能出现的病理生理过程的风险。
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In an experimental myocardial infarction model, L-arginine pre-intervention may exert cardioprotective effects by regulating OTULIN levels and mitochondrial dynamics.

The experimental myocardial infarction (MI) model originating from isoproterenol (ISO) is frequently preferred in research due to its similarity to MI-induced damage in humans. Beneficial effects of L-arginine (L-Arg), a semi-essential amino acid, in cardiovascular diseases have been shown in many studies. This study was carried out to determine whether L-Arg pre-intervention has protective effects on heart tissue in the experimental MI model. The 28 rats used in the study were randomly divided into 4 equal groups: control, L-Arg, ISO, and L-Arg+ISO. Upon completion of all applications, cardiac markers in serum and biochemical, histopathological, and immunohistochemical examinations in cardiac tissues were performed. Cardiac markers, histopathological changes, oxidative stress, inflammation, and apoptosis were increased in the experimental MI model. In addition, administration of ISO deregulated OTULIN levels and mitochondrial dynamics in heart tissue. However, L-Arg pre-intervention showed a significant protective effect against changes in ISO-induced MI. L-Arg supplementation with cardioprotective effect may reduce the risks of possible pathophysiological processes in MI.

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4.30%
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