Liu Hongqun, Hwang Sang-Youn, Lee Samuel S
Liver Unit, University of Calgary Cumming School of Medicine, Calgary, AB T2N 4N1, Canada.
Department of Internal Medicine, Dongnam Institute of Radiological & Medical Sciences, Busan 46033, Republic of Korea.
Pharmaceuticals (Basel). 2023 Jul 7;16(7):978. doi: 10.3390/ph16070978.
Abnormal cardiac function in the setting of cirrhosis and in the absence of a primary cardiac disease is known as cirrhotic cardiomyopathy. The pathogenesis of cirrhotic cardiomyopathy is multifactorial but broadly is comprised of two pathways. The first is due to cirrhosis and synthetic liver failure with abnormal structure and function of many substances, including proteins, lipids, hormones, and carbohydrates such as lectins. The second is due to portal hypertension which invariably accompanies cirrhosis. Portal hypertension leads to a leaky, congested gut with resultant endotoxemia and systemic inflammation. This inflammatory phenotype comprises oxidative stress, cellular apoptosis, and inflammatory cell infiltration. Galectins exert all these pro-inflammatory mechanisms across many different tissues and organs, including the heart. Effective therapies for improving cardiac function in patients with cirrhosis are not available. Conventional strategies for other noncirrhotic heart diseases, including vasodilators, are not feasible because of the significant baseline vasodilation in cirrhotic patients. Therefore, exploring new treatment modalities for cirrhotic cardiomyopathy is of great importance. Galectin-3 inhibitors such as modified citrus pectin, N-acetyllactosamine, TD139 and GB0139 exert anti-apoptotic, anti-oxidative and anti-inflammatory effects and thus have potential therapeutic interest. This review briefly summarizes the physiological and pathophysiological role of galectin and specifically examines its role in cardiac disease processes. We present a more detailed discussion of galectin in cardiovascular complications of cirrhosis, particularly cirrhotic cardiomyopathy. Finally, therapeutic studies of galectin-3 inhibitors in cirrhotic cardiomyopathy are reviewed.
在肝硬化背景下且无原发性心脏疾病时出现的心脏功能异常被称为肝硬化性心肌病。肝硬化性心肌病的发病机制是多因素的,但大致可分为两条途径。第一条途径是由于肝硬化和肝脏合成功能衰竭,导致包括蛋白质、脂质、激素以及如凝集素等碳水化合物在内的许多物质的结构和功能异常。第二条途径是由于门静脉高压,而门静脉高压总是伴随着肝硬化。门静脉高压导致肠道渗漏、充血,进而引发内毒素血症和全身炎症。这种炎症表型包括氧化应激、细胞凋亡和炎症细胞浸润。半乳凝素在包括心脏在内的许多不同组织和器官中发挥所有这些促炎机制。目前尚无改善肝硬化患者心脏功能的有效疗法。对于其他非肝硬化性心脏病的传统治疗策略,如血管扩张剂,由于肝硬化患者存在显著的基线血管扩张,因此不可行。因此,探索肝硬化性心肌病的新治疗方法非常重要。诸如改性柑橘果胶、N-乙酰乳糖胺、TD139和GB0139等半乳凝素-3抑制剂具有抗凋亡、抗氧化和抗炎作用,因此具有潜在的治疗价值。本综述简要总结了半乳凝素的生理和病理生理作用,并特别研究了其在心脏疾病过程中的作用。我们更详细地讨论了半乳凝素在肝硬化心血管并发症,特别是肝硬化性心肌病中的作用。最后,综述了半乳凝素-3抑制剂在肝硬化性心肌病中的治疗研究。