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急性和慢性替拉塞米治疗改善基于肌动蛋白的线状体肌病小鼠的体内和体外肌肉性能。

Acute and chronic tirasemtiv treatment improves in vivo and in vitro muscle performance in actin-based nemaline myopathy mice.

机构信息

Department of Physiology, Amsterdam UMC (location VUmc), Amsterdam 1081 HV, The Netherlands.

Aix-Marseille Univ, CNRS, CRMBM, UMR 7339, 13005 Marseille, France.

出版信息

Hum Mol Genet. 2021 Jun 26;30(14):1305-1320. doi: 10.1093/hmg/ddab112.

DOI:10.1093/hmg/ddab112
PMID:33909041
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8255131/
Abstract

Nemaline myopathy, a disease of the actin-based thin filament, is one of the most frequent congenital myopathies. To date, no specific therapy is available to treat muscle weakness in nemaline myopathy. We tested the ability of tirasemtiv, a fast skeletal troponin activator that targets the thin filament, to augment muscle force-both in vivo and in vitro-in a nemaline myopathy mouse model with a mutation (H40Y) in Acta1. In Acta1H40Y mice, treatment with tirasemtiv increased the force response of muscles to submaximal stimulation frequencies. This resulted in a reduced energetic cost of force generation, which increases the force production during a fatigue protocol. The inotropic effects of tirasemtiv were present in locomotor muscles and, albeit to a lesser extent, in respiratory muscles, and they persisted during chronic treatment, an important finding as respiratory failure is the main cause of death in patients with congenital myopathy. Finally, translational studies on permeabilized muscle fibers isolated from a biopsy of a patient with the ACTA1H40Y mutation revealed that at physiological Ca2+ concentrations, tirasemtiv increased force generation to values that were close to those generated in muscle fibers of healthy subjects. These findings indicate the therapeutic potential of fast skeletal muscle troponin activators to improve muscle function in nemaline myopathy due to the ACTA1H40Y mutation, and future studies should assess their merit for other forms of nemaline myopathy and for other congenital myopathies.

摘要

先天性肌营养不良症是一种以肌动蛋白为基础的细肌丝疾病,是最常见的先天性肌病之一。迄今为止,尚无针对先天性肌营养不良症肌肉无力的特定治疗方法。我们测试了靶向细肌丝的快速骨骼肌肌钙蛋白激活剂替拉塞米的能力,以增强 Actal 突变(H40Y)的先天性肌营养不良症小鼠模型中的肌肉力量-无论是在体内还是在体外。在 ActalH40Y 小鼠中,替拉塞米治疗可增加肌肉对亚最大刺激频率的力反应。这导致产生力的能量成本降低,从而增加疲劳协议期间的力产生。替拉塞米的变力效应存在于运动肌肉中,尽管程度较小,但在呼吸肌肉中也存在,并且在慢性治疗期间仍然存在,这是一个重要的发现,因为呼吸衰竭是先天性肌病患者死亡的主要原因。最后,对从患有 ACTA1H40Y 突变的患者活检中分离出的通透性肌纤维进行的转化研究表明,在生理 Ca2+浓度下,替拉塞米可增加力的产生,使其接近健康受试者肌纤维产生的力。这些发现表明,快速骨骼肌肌钙蛋白激活剂具有治疗先天性肌营养不良症的潜力,可改善由于 ActalH40Y 突变引起的肌肉功能,未来的研究应评估其在其他形式的先天性肌营养不良症和其他先天性肌病中的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8faa/8255131/860693448373/ddab112f7.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8faa/8255131/860693448373/ddab112f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8faa/8255131/c59814e28f95/ddab112f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8faa/8255131/6898df845c44/ddab112f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8faa/8255131/9e01c683a824/ddab112f3.jpg
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