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联合 MRI 和 ³¹P-MRS 研究 ACTA1(H40Y) 基因突变肌病小鼠模型,显示肌肉功能受损和能量代谢改变。

Combined MRI and ³¹P-MRS investigations of the ACTA1(H40Y) mouse model of nemaline myopathy show impaired muscle function and altered energy metabolism.

机构信息

Aix-Marseille Université, Centre National de la Recherche Scientifique (CNRS), Centre de Résonance Magnétique Biologique et Médicale (CRMBM) Unité Mixte de Recherche (UMR), Marseille, France.

出版信息

PLoS One. 2013 Apr 16;8(4):e61517. doi: 10.1371/journal.pone.0061517. Print 2013.

Abstract

Nemaline myopathy (NM) is the most common disease entity among non-dystrophic skeletal muscle congenital diseases. Mutations in the skeletal muscle α-actin gene (ACTA1) account for ∼25% of all NM cases and are the most frequent cause of severe forms of NM. So far, the mechanisms underlying muscle weakness in NM patients remain unclear. Additionally, recent Magnetic Resonance Imaging (MRI) studies reported a progressive fatty infiltration of skeletal muscle with a specific muscle involvement in patients with ACTA1 mutations. We investigated strictly noninvasively the gastrocnemius muscle function of a mouse model carrying a mutation in the ACTA1 gene (H40Y). Skeletal muscle anatomy (hindlimb muscles and fat volumes) and energy metabolism were studied using MRI and (31)Phosphorus magnetic resonance spectroscopy. Skeletal muscle contractile performance was investigated while applying a force-frequency protocol (from 1-150 Hz) and a fatigue protocol (80 stimuli at 40 Hz). H40Y mice showed a reduction of both absolute (-40%) and specific (-25%) maximal force production as compared to controls. Interestingly, muscle weakness was associated with an improved resistance to fatigue (+40%) and an increased energy cost. On the contrary, the force frequency relationship was not modified in H40Y mice and the extent of fatty infiltration was minor and not different from the WT group. We concluded that the H40Y mouse model does not reproduce human MRI findings but shows a severe muscle weakness which might be related to an alteration of intrinsic muscular properties. The increased energy cost in H40Y mice might be related to either an impaired mitochondrial function or an alteration at the cross-bridges level. Overall, we provided a unique set of anatomic, metabolic and functional biomarkers that might be relevant for monitoring the progression of NM disease but also for assessing the efficacy of potential therapeutic interventions at a preclinical level.

摘要

先天性非营养不良性骨骼肌疾病中以杆状体肌病(nemaline myopathy,NM)最为常见。骨骼肌α-肌动蛋白基因(skeletal muscle α-actin gene,ACTA1)的突变占所有 NM 病例的约 25%,是 NM 严重型最常见的病因。目前,NM 患者肌肉无力的机制仍不清楚。此外,最近的磁共振成像(Magnetic Resonance Imaging,MRI)研究报道了携带 ACTA1 突变的患者骨骼肌进行性脂肪浸润和特定肌肉受累。我们使用 MRI 和(31)磷磁共振波谱(Phosphorus magnetic resonance spectroscopy),严格非侵入性地研究了携带 ACTA1 基因突变(H40Y)的小鼠模型的腓肠肌功能。研究了骨骼肌解剖结构(后肢肌肉和脂肪量)和能量代谢,同时应用力频率方案(1-150 Hz)和疲劳方案(40 Hz 时 80 次刺激)研究骨骼肌收缩性能。与对照组相比,H40Y 小鼠的绝对(-40%)和特定(-25%)最大力产生均减少。有趣的是,肌肉无力与抗疲劳能力提高(+40%)和能量消耗增加有关。相反,H40Y 小鼠的力频率关系没有改变,脂肪浸润程度较小,与 WT 组无差异。我们得出结论,H40Y 小鼠模型不能复制人类 MRI 发现,但表现出严重的肌肉无力,这可能与内在肌肉特性的改变有关。H40Y 小鼠的能量消耗增加可能与线粒体功能受损或横桥水平的改变有关。总之,我们提供了一组独特的解剖、代谢和功能生物标志物,这些标志物可能与 NM 疾病的进展监测有关,也可能与临床前水平评估潜在治疗干预的疗效有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/073f/3629063/339a0cd75ab9/pone.0061517.g001.jpg

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