de Dios Elena, Forteza Maria J, Perez-Sole Nerea, Molina-Garcia Tamara, Gavara Jose, Marcos-Garces Victor, Jimenez-Navarro Manuel, Ruiz-Sauri Amparo, Rios-Navarro Cesar, Bodi Vicente
Centro de Investigación Biomédica en Red-Cardiovascular, 28029 Madrid, Spain.
Cardiovascular Medicine Unit, Center of Molecular Medicine, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, 17176 Stockholm, Sweden.
Int J Mol Sci. 2025 Sep 10;26(18):8820. doi: 10.3390/ijms26188820.
Although cardiac metabolic adaptation has been observed in response to the ischemia-reperfusion, the specific temporal and spatial changes occurring in the main regulators of myocardial glucolipid metabolism in the infarcted heart have not been fully characterized. Myocardial infarction (MI) was induced in female swine by transient coronary occlusion. The study design consisted of one control and four MI groups (no reperfusion, 1 min, 1 week, and 1 month after reperfusion). Metabolites obtained from the coronary sinus were determined at baseline, during ischemia, and after coronary reperfusion. mRNA expression of genes related to beta-oxidation and glucose transport were quantified in the five experimental groups and in three myocardial regions (infarcted, adjacent, and remote). In the coronary sinus, reduced glucose and increased lactate levels were detected during ischemia and soon after reperfusion. However, non-esterified fatty acids increased during reperfusion. A general upregulation of genes implicated in glycolysis and beta-oxidation occurred during ischemia and few minutes after reperfusion. Contrarily, heightened mRNA expression of glucose transporters and decay in regulators of beta-oxidation were observed one week after coronary reperfusion. Glycolysis and beta-oxidation are activated during ischemia and few minutes after coronary reopening, while a shift from beta-oxidation to glycolysis is evidenced a few days afterwards.
尽管已观察到心脏代谢适应缺血再灌注的现象,但梗死心脏中心肌糖脂代谢主要调节因子发生的特定时空变化尚未完全明确。通过短暂冠状动脉闭塞在雌性猪中诱导心肌梗死(MI)。研究设计包括一个对照组和四个MI组(再灌注前、再灌注后1分钟、1周和1个月)。在基线、缺血期间和冠状动脉再灌注后测定从冠状窦获得的代谢物。在五个实验组和三个心肌区域(梗死区、相邻区和远隔区)对与β氧化和葡萄糖转运相关基因的mRNA表达进行定量。在冠状窦中,缺血期间和再灌注后不久检测到葡萄糖水平降低和乳酸水平升高。然而,再灌注期间非酯化脂肪酸增加。在缺血期间和再灌注后几分钟,参与糖酵解和β氧化的基因普遍上调。相反,冠状动脉再灌注一周后观察到葡萄糖转运体的mRNA表达升高以及β氧化调节因子的衰减。糖酵解和β氧化在缺血期间和冠状动脉再通后几分钟被激活,而几天后则出现从β氧化向糖酵解的转变。