内皮功能受损导致心脏功能障碍--线粒体动力学的作用。

IF 4.1 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Cristhian A Gutierrez-Huerta, Giovanni Quiroz-Delfi, Fathima Dhilhani Mohammed Faleel, Andreas Beyer
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引用次数: 0

摘要

内皮微血管对调节血管舒张和血管收缩至关重要,内皮功能的改善与冠状动脉疾病(CAD)患者的预后改善有关。内皮功能障碍患者会丧失由 NO 介导的血管舒张功能,转而通过线粒体产生的 H2O2 实现血管舒张。线粒体动力学是一种重要的自动调节机制,有助于线粒体和内皮的平衡,并在活性氧(ROS)(包括 H2O2)的形成中发挥作用。线粒体动力学失调会导致 ROS 生成增加、ATP 生成减少、新陈代谢受损、病理信号转导激活、钙感应受损和炎症。我们推测,内皮线粒体动力学失调在 CAD 患者的内皮微血管功能障碍中起着至关重要的作用。因此,适当调节内皮线粒体动力学可能是治疗内皮微血管功能障碍患者的一种合适方法,而且我们进一步推测,改善这种微血管功能障碍将直接改善 CAD 患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impaired endothelial function contributes to cardiac dysfunction - role of mitochondrial dynamics.

The endothelial microvasculature is essential for the regulation of vasodilation and vasoconstriction, and improved functioning of the endothelium is linked to improved outcomes for individuals with coronary artery disease (CAD). People with endothelial dysfunction exhibit a loss of NO-mediated vasodilation, achieving vasodilation instead through mitochondria-derived H2O2. Mitochondrial dynamics is an important autoregulatory mechanism that contributes to mitochondrial and endothelial homeostasis and plays a role in formation of reactive oxygen species (ROS), including H2O2. Dysregulation of mitochondrial dynamics leads to increased ROS production, decreased ATP production, impaired metabolism, activation of pathological signal transduction, impaired calcium sensing, and inflammation. We hypothesize that dysregulation of endothelial mitochondrial dynamics plays a crucial role in the endothelial microvascular dysfunction seen in individuals with CAD. Therefore, proper regulation of endothelial mitochondrial dynamics may be a suitable treatment for individuals with endothelial microvascular dysfunction and we furthermore postulate that improving this microvascular dysfunction will directly improve outcomes for those with CAD.

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来源期刊
CiteScore
9.60
自引率
10.40%
发文量
202
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.
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