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线粒体功能障碍作为介导帕金森病心脏合并症的潜在机制。

Mitochondrial Dysfunction as a Potential Mechanism Mediating Cardiac Comorbidities in Parkinson's Disease.

机构信息

The Roslin Institute and R(D)SVS, University of Edinburgh, Easter Bush, Midlothian EH25 9RH, UK.

EaStCHEM School of Chemistry, University of Edinburgh, Edinburgh EH9 3FJ, UK.

出版信息

Int J Mol Sci. 2024 Oct 12;25(20):10973. doi: 10.3390/ijms252010973.

Abstract

Individuals diagnosed with Parkinson's disease (PD) often exhibit heightened susceptibility to cardiac dysfunction, reflecting a complex interaction between these conditions. The involvement of mitochondrial dysfunction in the development and progression of cardiac dysfunction and PD suggests a plausible commonality in some aspects of their molecular pathogenesis, potentially contributing to the prevalence of cardiac issues in PD. Mitochondria, crucial organelles responsible for energy production and cellular regulation, play important roles in tissues with high energetic demands, such as neurons and cardiac cells. Mitochondrial dysfunction can occur in different and non-mutually exclusive ways; however, some mechanisms include alterations in mitochondrial dynamics, compromised bioenergetics, biogenesis deficits, oxidative stress, impaired mitophagy, and disrupted calcium balance. It is plausible that these factors contribute to the increased prevalence of cardiac dysfunction in PD, suggesting mitochondrial health as a potential target for therapeutic intervention. This review provides an overview of the physiological mechanisms underlying mitochondrial quality control systems. It summarises the diverse roles of mitochondria in brain and heart function, highlighting shared pathways potentially exhibiting dysfunction and driving cardiac comorbidities in PD. By highlighting strategies to mitigate dysfunction associated with mitochondrial impairment in cardiac and neural tissues, our review aims to provide new perspectives on therapeutic approaches.

摘要

个体患有帕金森病(PD)时往往表现出对心脏功能障碍的高度易感性,反映了这些疾病之间的复杂相互作用。线粒体功能障碍在心脏功能障碍和 PD 的发生和发展中的参与表明,它们在分子发病机制的某些方面具有一定的共同性,这可能导致 PD 中心脏问题的高发。线粒体是负责能量产生和细胞调节的关键细胞器,在需要高能量的组织中发挥着重要作用,如神经元和心肌细胞。线粒体功能障碍可能以不同的、非相互排斥的方式发生;然而,一些机制包括线粒体动力学的改变、生物能量学受损、生物发生缺陷、氧化应激、受损的自噬和钙平衡破坏。这些因素可能导致 PD 中心脏功能障碍的高发,表明线粒体健康是治疗干预的潜在靶点。这篇综述概述了线粒体质量控制系统的生理机制。它总结了线粒体在大脑和心脏功能中的多种作用,强调了可能表现出功能障碍并导致 PD 中心律失常的共享途径。通过强调减轻与心脏和神经组织中线粒体损伤相关的功能障碍的策略,我们的综述旨在为治疗方法提供新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebbd/11507255/38a36403ff1b/ijms-25-10973-g001.jpg

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