Department of Pharmacology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Department of Pharmacology, Faculty of Pharmacy, Mahidol University, Bangkok 10400, Thailand.
Int J Mol Sci. 2024 May 25;25(11):5763. doi: 10.3390/ijms25115763.
Cardiovascular diseases (CVDs), particularly heart failure, are major contributors to early mortality globally. Heart failure poses a significant public health problem, with persistently poor long-term outcomes and an overall unsatisfactory prognosis for patients. Conventionally, treatments for heart failure have focused on lowering blood pressure; however, the development of more potent therapies targeting hemodynamic parameters presents challenges, including tolerability and safety risks, which could potentially restrict their clinical effectiveness. Adenosine has emerged as a key mediator in CVDs, acting as a retaliatory metabolite produced during cellular stress via ATP metabolism, and works as a signaling molecule regulating various physiological processes. Adenosine functions by interacting with different adenosine receptor (AR) subtypes expressed in cardiac cells, including AAR, AAR, AAR, and AAR. In addition to AAR, AAR has a multifaceted role in the cardiovascular system, since its activation contributes to reducing the damage to the heart in various pathological states, particularly ischemic heart disease, heart failure, and hypertension, although its role is not as well documented compared to other AR subtypes. Research on AAR signaling has focused on identifying the intricate molecular mechanisms involved in CVDs through various pathways, including G or G protein-dependent signaling, ATP-sensitive potassium channels, MAPKs, and G protein-independent signaling. Several AAR-specific agonists, such as piclidenoson and namodenoson, exert cardioprotective impacts during ischemia in the diverse animal models of heart disease. Thus, modulating AARs serves as a potential therapeutic approach, fueling considerable interest in developing compounds that target AARs as potential treatments for heart diseases.
心血管疾病(CVDs),尤其是心力衰竭,是全球早逝的主要原因。心力衰竭是一个重大的公共卫生问题,长期预后一直不佳,患者总体预后不理想。传统上,心力衰竭的治疗侧重于降低血压;然而,针对血流动力学参数的更有效的治疗方法的发展存在挑战,包括耐受性和安全性风险,这可能限制其临床效果。腺苷已成为 CVDs 的主要介质,作为细胞应激通过 ATP 代谢产生的报复性代谢物,作为调节各种生理过程的信号分子发挥作用。腺苷通过与心脏细胞中表达的不同腺苷受体(AR)亚型相互作用发挥作用,包括 AAR、AAR、AAR 和 AAR。除了 AAR,AAR 在心血管系统中具有多方面的作用,因为其激活有助于减少各种病理状态下对心脏的损伤,特别是缺血性心脏病、心力衰竭和高血压,尽管与其他 AR 亚型相比,其作用尚未得到充分记录。AAR 信号转导的研究侧重于通过各种途径(包括 G 或 G 蛋白依赖性信号转导、ATP 敏感性钾通道、MAPK 和 G 蛋白非依赖性信号转导)确定与 CVDs 相关的复杂分子机制。几种 AAR 特异性激动剂,如 piclidenoson 和 namodenoson,在各种心脏病动物模型的缺血中发挥心脏保护作用。因此,调节 AAR 可能是一种潜在的治疗方法,这激发了人们对开发靶向 AAR 的化合物作为潜在心脏病治疗方法的极大兴趣。