Knight Walter E, Woulfe Kathleen C
Division of Cardiology, Department of Medicine, University of Colorado Anschutz Medical Campus, 12700 E 19 Ave, Aurora, CO 80045.
Curr Opin Physiol. 2022 Apr;26. doi: 10.1016/j.cophys.2022.100535. Epub 2022 Apr 1.
Since cardiac relaxation is commonly impaired in heart failure caused by many different etiologies, identifying druggable targets is a common goal. While many factors contribute to cardiac relaxation, this review focuses on sarcomeric relaxation and dysfunction. Any alteration in how sarcomeric proteins interact can lead to significant shifts in sarcomeric relaxation that may contribute to diastolic dysfunction. Considering examples of sarcomeric dysfunction that have been reported in 3 different pathologies, hypertrophic cardiomyopathy, restrictive cardiomyopathy, and heart failure with preserved ejection fraction, will provide insights into the role sarcomeric dysfunction plays in impaired cardiac relaxation. This will ultimately improve our understanding of sarcomeric physiology and uncover new therapeutic targets.
由于在由多种不同病因引起的心力衰竭中,心脏舒张功能通常会受损,因此确定可药物作用的靶点是一个共同目标。虽然有许多因素会影响心脏舒张,但本综述重点关注肌节舒张和功能障碍。肌节蛋白相互作用方式的任何改变都可能导致肌节舒张发生显著变化,这可能会导致舒张功能障碍。考虑到在肥厚型心肌病、限制型心肌病和射血分数保留的心力衰竭这三种不同病理中报道的肌节功能障碍实例,将有助于深入了解肌节功能障碍在心脏舒张受损中所起的作用。这最终将增进我们对肌节生理学的理解,并发现新的治疗靶点。