Porcari Paola, Hall Matt G, Clark Chris A, Greally Elizabeth, Straub Volker, Blamire Andrew M
Institute of Genetic Medicine and Centre for In Vivo Imaging, Newcastle University, Newcastle-upon-Tyne, UK.
Developmental Imaging and Biophysics Section, UCL GOS Institute of Child Health, University College London, London, UK.
NMR Biomed. 2018 Mar;31(3). doi: 10.1002/nbm.3881. Epub 2018 Jan 9.
The investigation of age-related changes in muscle microstructure between developmental and healthy adult mice may help us to understand the clinical features of early-onset muscle diseases, such as Duchenne muscular dystrophy. We investigated the evolution of mouse hind-limb muscle microstructure using diffusion imaging of in vivo and in vitro samples from both actively growing and mature mice. Mean apparent diffusion coefficients (ADCs) of the gastrocnemius and tibialis anterior muscles were determined as a function of diffusion time (Δ), age (7.5, 22 and 44 weeks) and diffusion gradient direction, applied parallel or transverse to the principal axis of the muscle fibres. We investigated a wide range of diffusion times with the goal of probing a range of diffusion lengths characteristic of muscle microstructure. We compared the diffusion time-dependent ADC of hind-limb muscles with histology. ADC was found to vary as a function of diffusion time in muscles at all stages of maturation. Muscle water diffusivity was higher in younger (7.5 weeks) than in adult (22 and 44 weeks) mice, whereas no differences were observed between the older ages. In vitro data showed the same diffusivity pattern as in vivo data. The highlighted differences in diffusion properties between young and mature muscles suggested differences in underlying muscle microstructure, which were confirmed by histological assessment. In particular, although diffusion was more restricted in older muscle, muscle fibre size increased significantly from young to adult age. The extracellular space decreased with age by only ~1%. This suggests that the observed diffusivity differences between young and adult muscles may be caused by increased membrane permeability in younger muscle associated with properties of the sarcolemma.
研究发育中的小鼠与健康成年小鼠肌肉微观结构的年龄相关变化,可能有助于我们了解早发性肌肉疾病(如杜兴氏肌营养不良症)的临床特征。我们使用来自活跃生长和成熟小鼠的体内和体外样本的扩散成像,研究了小鼠后肢肌肉微观结构的演变。测定了腓肠肌和胫骨前肌的平均表观扩散系数(ADC),作为扩散时间(Δ)、年龄(7.5、22和44周)以及与肌纤维主轴平行或垂直施加的扩散梯度方向的函数。我们研究了广泛的扩散时间,目的是探测一系列肌肉微观结构特征性的扩散长度。我们将后肢肌肉的扩散时间依赖性ADC与组织学进行了比较。发现在所有成熟阶段,肌肉中的ADC均随扩散时间而变化。年轻(7.5周)小鼠的肌肉水扩散率高于成年(22和44周)小鼠,而老年小鼠之间未观察到差异。体外数据显示出与体内数据相同的扩散模式。年轻和成熟肌肉在扩散特性上的显著差异表明其潜在肌肉微观结构存在差异,这一点通过组织学评估得到了证实。特别是,尽管老年肌肉中的扩散受到更多限制,但从幼年到成年,肌纤维大小显著增加。细胞外空间随年龄仅减少约1%。这表明,观察到的年轻和成年肌肉之间的扩散率差异可能是由于年轻肌肉中与肌膜特性相关的膜通透性增加所致。