University of Nicosia Medical School, 21 Ilia Papakyriakou, 2414 Engomi, P.O. Box 24005, CY-1700 Nicosia, Cyprus.
Eur J Pharmacol. 2018 Aug 15;833:314-319. doi: 10.1016/j.ejphar.2018.06.029. Epub 2018 Jun 20.
A few decades ago, cardiac muscle was discovered to possess signalling pathways that, when activated, protect the myocardium against the damage induced by ischaemia-reperfusion. The ability of cardiac muscle to protect itself against injury has been termed 'cardioprotection'. Many compounds and procedures can trigger cardioprotection including conditionings (exposure to brief episodes of ischaemia-reperfusion to protect against sustained ischaemia-reperfusion), hypoxia, adenosine, acetylcholine, adrenomedullin, angiotensin, bradykinin, catecholamines, endothelin, estrogens, phenylephrine, opioids, testosterone, and many more. These triggers activate many intracellular signalling factors including protein kinases, different enzymes, transcription factors and defined signalling pathways to target structures in mitochondria, sarcoplasmic reticulum, nucleus and sarcolemma to mediate cardioprotection. Although a lot of information about cardioprotection has been acquired, there are still two major outstanding issues to be addressed in the future 1) better understanding of spatio-temporal relationships between signalling elements, and; 2) devising therapeutic strategies against myocardial diseases based on cardioprotective signalling. Further research is required to paint integral picture of cardioprotective signalling and more clinical studies are required to properly test clinical efficacy and safety of potential cardioprotective strategies. Therapies against cardiac diseases based on cardioprotective strategies would be a perfect adjunct to current therapeutic strategies based on restitution of coronary blood flow and regulation of myocardial metabolic demands.
几十年前,人们发现心肌具有信号通路,这些信号通路被激活后,可以保护心肌免受缺血再灌注引起的损伤。心肌自身对抗损伤的能力被称为“心脏保护”。许多化合物和程序都可以触发心脏保护,包括预处理(短暂暴露于缺血再灌注以防止持续的缺血再灌注)、缺氧、腺苷、乙酰胆碱、肾上腺髓质素、血管紧张素、缓激肽、儿茶酚胺、内皮素、雌激素、苯肾上腺素、阿片类药物、睾丸激素等等。这些触发因素激活了许多细胞内信号因子,包括蛋白激酶、不同的酶、转录因子和特定的信号通路,以靶向线粒体、肌浆网、核和肌膜中的结构,介导心脏保护。尽管已经获得了大量关于心脏保护的信息,但未来仍有两个主要的未解决问题需要解决:1)更好地理解信号元件之间的时空关系;2)设计基于心脏保护信号的心肌疾病治疗策略。需要进一步的研究来描绘心脏保护信号的整体图景,并且需要更多的临床研究来正确测试潜在心脏保护策略的临床疗效和安全性。基于心脏保护策略的心脏疾病治疗将是当前基于恢复冠状动脉血流和调节心肌代谢需求的治疗策略的完美补充。