线粒体生物发生
心肌保护
医学
粒体自噬
西妥因1
尼泊尔卢比1
锡尔图因
线粒体
再灌注损伤
TFAM公司
内科学
心功能曲线
肌酸激酶
褪黑素
缺血
内分泌学
心脏病学
生物
细胞凋亡
心力衰竭
细胞生物学
下调和上调
生物化学
自噬
乙酰化
基因
作者
Behnaz Mokhtari,Mitra Delkhah,Reza Badalzadeh,Samad Ghaffari
摘要
Abstract 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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