Brown R Dale, Ambler S Kelly, Mitchell M Darren, Long Carlin S
Division of Cardiology, University of Colorado Health Sciences Center, Denver, Colorado 80262, USA.
Annu Rev Pharmacol Toxicol. 2005;45:657-87. doi: 10.1146/annurev.pharmtox.45.120403.095802.
Cardiac fibroblasts play a central role in the maintenance of extracellular matrix in the normal heart and as mediators of inflammatory and fibrotic myocardial remodeling in the injured and failing heart. In this review, we evaluate the cardiac fibroblast as a therapeutic target in heart disease. Unique features of cardiac fibroblast cell biology are discussed in relation to normal and pathophysiological cardiac function. The contribution of cardiac fibrosis as an independent risk factor in the outcome of heart failure is considered. Candidate drug therapies that derive benefit from actions on cardiac fibroblasts are summarized, including inhibitors of angiotensin-aldosterone systems, endothelin receptor antagonists, statins, anticytokine therapies, matrix metalloproteinase inhibitors, and novel antifibrotic/anti-inflammatory agents. These findings point the way to future challenges in cardiac fibroblast biology and pharmacotherapy.
心脏成纤维细胞在正常心脏中维持细胞外基质起着核心作用,在受损和衰竭心脏中作为炎症和纤维化心肌重塑的介质。在本综述中,我们评估心脏成纤维细胞作为心脏病治疗靶点的情况。讨论了心脏成纤维细胞生物学的独特特征与正常和病理生理心脏功能的关系。考虑了心脏纤维化作为心力衰竭预后独立危险因素的作用。总结了从作用于心脏成纤维细胞中获益的候选药物疗法,包括血管紧张素 - 醛固酮系统抑制剂、内皮素受体拮抗剂、他汀类药物、抗细胞因子疗法、基质金属蛋白酶抑制剂和新型抗纤维化/抗炎药物。这些发现为心脏成纤维细胞生物学和药物治疗未来的挑战指明了方向。