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Exercise Training Preserves Ischemic Preconditioning in Aged Rat Hearts by Restoring the Myocardial Polyamine Pool

机译:运动训练可通过恢复心肌多胺池来维持老年大鼠心脏的缺血预处理

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Background. Ischemic preconditioning (IPC) strongly protects against myocardial ischemia reperfusion (IR) injury. However, IPC protection is ineffective in aged hearts. Exercise training reduces the incidence of age-related cardiovascular disease and upregulates the ornithine decarboxylase (ODC)/polyamine pathway. The aim of this study was to investigate whether exercise can reestablish IPC protection in aged hearts and whether IPC protection is linked to restoration of the cardiac polyamine pool.Methods. Rats aging 3 or 18 months perform treadmill exercises with or without gradient respectively for 6 weeks. Isolated hearts and isolated cardiomyocytes were exposed to an IR and IPC protocol.Results. IPC induced an increase in myocardial polyamines by regulating ODC and spermidine/spermine acetyltransferase (SSAT) in young rat hearts, but IPC did not affect polyamine metabolism in aged hearts. Exercise training inhibited the loss of preconditioning protection and restored the polyamine pool by activating ODC and inhibiting SSAT in aged hearts. An ODC inhibitor,α-difluoromethylornithine, abolished the recovery of preconditioning protection mediated by exercise. Moreover, polyamines improved age-associated mitochondrial dysfunctionin vitro.Conclusion. Exercise appears to restore preconditioning protection in aged rat hearts, possibly due to an increase in intracellular polyamines and an improvement in mitochondrial function in response to a preconditioning stimulus.
机译:背景。缺血预处理(IPC)可以强烈防止心肌缺血再灌注(IR)损伤。但是,IPC保护对老年心脏无效。运动训练可降低与年龄有关的心血管疾病的发生率,并上调鸟氨酸脱羧酶(ODC)/多胺途径。这项研究的目的是调查运动是否可以在老年心脏中重新建立IPC保护,以及IPC保护是否与心脏多胺库的恢复有关。 3个月或18个月大的大鼠分别在有或没有梯度的情况下进行跑步机运动,持续6周。将离体心脏和离体心肌细胞暴露于IR和IPC方案中。结果。 IPC通过调节年轻大鼠心脏中的ODC和亚精胺/亚精胺乙酰转移酶(SSAT)诱导心肌多胺增加,但IPC不会影响老年心脏中的多胺代谢。运动训练通过激活ODC和抑制老年心脏中的SSAT抑制了预处理保护的丧失,并恢复了多胺库。 ODC抑制剂α-二氟甲基鸟氨酸消除了运动介导的预处理保护的恢复。此外,多胺在体外改善了年龄相关的线粒体功能障碍。运动似乎可以恢复老年大鼠心脏的预处理保护,这可能是由于细胞内多胺的增加以及响应预处理刺激而线粒体功能的改善所致。

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