揭示活化蛋白C(APC)在减轻再灌注损伤和心脏缺血中的分子机制:新的治疗干预措施的前景。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2024-04-01 Epub Date: 2023-10-18 DOI:10.1007/s12265-023-10445-y
Nishant Johri, Prithpal S Matreja, Shalabh Agarwal, Priya Nagar, Deepanshu Kumar, Aditya Maurya
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引用次数: 0

摘要

缺血性心脏病是由冠状动脉斑块形成引起的,它阻碍了含氧血液流向心脏,导致局部缺血。再灌注损伤仍然是研究人员面临的重大挑战,心肌缺血再灌注损伤(MIRI)的潜在机制尚不完全清楚。该综述基于我们目前对MIRI病理生理机制的理解,指导未来临床治疗中潜在靶点的研究。该研究为MIRI的潜在机制提供了见解,并为该领域的未来研究提供了方向。靶向治疗的使用可能有望改善老年人的心脏功能,并最大限度地减少血运重建治疗的不良影响。这篇综述的目的是分析活化蛋白C(APC)在缺血性心脏病、心力衰竭和心肌缺血再灌注损伤的发病机制中的作用,并讨论基于APC的治疗方法的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Unraveling the Molecular Mechanisms of Activated Protein C (APC) in Mitigating Reperfusion Injury and Cardiac Ischemia: a Promising Avenue for Novel Therapeutic Interventions.

Unraveling the Molecular Mechanisms of Activated Protein C (APC) in Mitigating Reperfusion Injury and Cardiac Ischemia: a Promising Avenue for Novel Therapeutic Interventions.

Ischemic heart disease, which results from plaque formation in the coronary arteries, hinders the flow of oxygenated blood to the heart, leading to ischemia. Reperfusion injury remains a significant challenge for researchers, and the mechanisms underlying myocardial ischemia-reperfusion injury (MIRI) are not entirely understood. The review directs future research into potential targets in clinical treatment based on our present understanding of the pathophysiological mechanisms of MIRI. The study provides insights into the mechanisms underlying MIRI and offers direction for future research in this area. The use of targeted therapies may hold promise in improving cardiac function in the elderly and minimizing the adverse effects of revascularization therapies. The purpose of this review is to analyze the role of activated protein C (APC) in the pathogenesis of ischemic heart disease, heart failure, and myocardial ischemia-reperfusion injury, and discuss the potential of APC-based therapeutics.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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