[线粒体功能障碍对冠状动脉疾病的影响-第二部分]。

IF 0.9 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Nazl Do An, Neslihan Oban
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引用次数: 0

摘要

除了分子过程外,其功能因分子过程而改变的细胞器还参与了动脉粥样硬化的发病机制,动脉粥样硬化是冠状动脉疾病的主要原因。近年来,线粒体在冠状动脉疾病发病机制中的作用引起了研究者的关注。线粒体是一种细胞器,具有自己的基因组,在有氧呼吸、能量产生和细胞代谢中起调节作用。细胞中线粒体的数量是动态变化的,每个组织和细胞中线粒体的数量都是不同的,这取决于它们的功能和能量需求。氧化应激通过导致线粒体基因组和线粒体生物发生的改变而引起线粒体功能障碍。心血管系统线粒体群功能失调与冠状动脉疾病的发生过程和细胞死亡机制密切相关。在动脉粥样硬化过程中,线粒体(dys)功能的改变伴随分子的改变,将在不久的将来成为冠状动脉疾病新的治疗靶点之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Effect of Mitochondrial Dysfunction on Coronary Artery Disease - Part 2].

Organelles whose functions change as a result of molecular processes are involved in the pathogenesis of atherosclerosis, which is the main cause of coronary artery disease, in addition to molecular processes. Recently, the role of mitochondria in the pathogenesis of coronary artery disease has attracted the attention of researchers. Mitochondria is a cell organelle with its own genome that plays a regulatory role in aerobic respiration, energy production, and cell metabolism. The number of mitochondria in cells changes dynamically, and there are di���erent numbers of mitochondria in every tissue and every cell, depending on their function and energy needs. Oxidative stress causes mitochondrial dysfunction by leading to alterations in the mitochondrial genome and mitochondrial biogenesis. The dysfunctional mitochondria population in the cardiovascular system is closely related to the coronary artery disease process and cell death mechanisms. It is thought that the altered mitochondria (dys)function accompanying the molecular changes in the atherosclerosis process will be among the new therapeutic targets of coronary artery disease in the near future.

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来源期刊
CiteScore
1.30
自引率
12.50%
发文量
124
审稿时长
32 weeks
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