线粒体移植联合米托醌和褪黑素:老龄大鼠心肌再灌注损伤的生存策略。

IF 2.6 4区 医学 Q2 PHYSIOLOGY
Behnaz Mokhtari, Mitra Delkhah, Reza Badalzadeh, Samad Ghaffari
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引用次数: 0

摘要

心肌缺血-再灌注(IR)损伤对心脏健康构成严重威胁,特别是在老龄化人口中,由于线粒体功能与年龄相关的下降,对这种损伤的易感性显著增加,因此突出了线粒体作为创新疗法的关键靶点。本研究的目的是探讨线粒体移植和线粒体促进剂mitoquinone和褪黑素联合治疗老年大鼠心肌IR损伤的方法。选取22 ~ 24月龄雄性Wistar大鼠54只,随机分为IR损伤组和非IR损伤组,分别进行单独和联合治疗。暂时阻断和重开左冠状动脉前降支诱导心肌IR损伤。缺血前14天腹腔给予米托醌,再灌注开始时分别腹腔和心内给予褪黑素和分离的线粒体。最后,我们评估了血流动力学指标、肌酸激酶- mb水平、线粒体功能终点和线粒体生物发生基因表达的变化,包括sirtuin 1 (SIRT-1)、过氧化物酶体增殖体激活受体γ辅助激活因子1- α (PGC-1α)和核呼吸因子2 (NRF-2)。三联疗法增强老年IR大鼠心肌功能,降低肌酸激酶- mb水平,改善线粒体功能及线粒体生物发生基因表达。与单一或双重治疗相比,这种联合治疗方法具有显著的心脏保护作用。三联疗法通过增强SIRT-1/PGC-1α/NRF-2谱改善线粒体功能和生物发生,为老年大鼠心脏提供了实质性的心脏保护,这表明了减轻老年患者IR损伤的有希望的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitochondrial transplantation combined with mitoquinone and melatonin: A survival strategy against myocardial reperfusion injury in aged rats

Myocardial ischaemia–reperfusion (IR) injury poses a severe threat to cardiac health, particularly in the ageing population, where susceptibility to such damage is significantly heightened owing to age-related declines in mitochondrial function, thus highlighting mitochondria as crucial targets for innovative therapies. The aim of this study was to investigate the combined modality therapy involving mitochondrial transplantation and the mitochondrial boosters mitoquinone and melatonin to address myocardial IR injury in aged rats. A total of 54 male Wistar rats, aged 22–24 months, were randomly divided into groups that either received IR injury or not, and were subjected to various treatments, both individually and in combination. Myocardial IR injury was induced by temporarily blocking and reopening the left anterior descending coronary artery. Mitoquinone was given intraperitoneally for 14 days prior to ischaemia, while melatonin and isolated mitochondria were administered intraperitoneally and intramyocardially, respectively, at the onset of reperfusion. Finally, we evaluated changes in haemodynamic indices, creatine kinase-MB levels, mitochondrial function endpoints and the expression of mitochondrial biogenesis genes, including sirtuin 1 (SIRT-1), peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) and nuclear respiratory factor 2 (NRF-2). The triple therapy enhanced myocardial function, decreased creatine kinase-MB levels and improved mitochondrial function along with the expression of mitochondrial biogenesis genes in aged IR rats. This combined approach elicited significant cardioprotection in comparison to single or dual therapies. The triple therapy provided substantial cardioprotection in aged rat hearts by improving mitochondrial function and biogenesis through enhanced SIRT-1/PGC-1α/NRF-2 profiles, suggesting a promising strategy for mitigating IR injury in elderly patients.

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来源期刊
Experimental Physiology
Experimental Physiology 医学-生理学
CiteScore
5.10
自引率
3.70%
发文量
262
审稿时长
1 months
期刊介绍: Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged. Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.
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