4.6 Article

From fibre to function: are we accurately representing muscle architecture and performance?

期刊

BIOLOGICAL REVIEWS
卷 97, 期 4, 页码 1640-1676

出版社

WILEY
DOI: 10.1111/brv.12856

关键词

biomechanics; muscle; functional morphology; locomotion; modelling; physiology

类别

资金

  1. Leverhulme Trust [RPG-2017-296]
  2. BBSRC [BB/R016380/1, BB/R016917/1, BB/R017190/1]
  3. BBSRC [BB/R017190/1, BB/R016917/1, BB/R016380/1] Funding Source: UKRI

向作者/读者索取更多资源

The size and arrangement of muscle fibers play a crucial role in their kinetic and energetic performance. However, previous studies have relied on a small number of fiber measurements to quantify muscle architectural properties, leading to potentially large errors. This study addresses this issue by combining medical imaging, statistical analysis, and computer simulation, and demonstrates the significant impact of errors in fiber architecture characterization on the prediction of in-vivo dynamics and muscle function, as well as the assessment of muscle specialization across species. These findings have important implications for a wide range of research fields.
The size and arrangement of fibres play a determinate role in the kinetic and energetic performance of muscles. Extrapolations between fibre architecture and performance underpin our understanding of how muscles function and how they are adapted to power specific motions within and across species. Here we provide a synopsis of how this 'fibre to function' paradigm has been applied to understand muscle design, performance and adaptation in animals. Our review highlights the widespread application of the fibre to function paradigm across a diverse breadth of biological disciplines but also reveals a potential and highly prevalent limitation running through past studies. Specifically, we find that quantification of muscle architectural properties is almost universally based on an extremely small number of fibre measurements. Despite the volume of research into muscle properties, across a diverse breadth of research disciplines, the fundamental assumption that a small proportion of fibre measurements can accurately represent the architectural properties of a muscle has never been quantitatively tested. Subsequently, we use a combination of medical imaging, statistical analysis, and physics-based computer simulation to address this issue for the first time. By combining diffusion tensor imaging (DTI) and deterministic fibre tractography we generated a large number of fibre measurements (>3000) rapidly for individual human lower limb muscles. Through statistical subsampling simulations of these measurements, we demonstrate that analysing a small number of fibres (n < 25) typically used in previous studies may lead to extremely large errors in the characterisation of overall muscle architectural properties such as mean fibre length and physiological cross-sectional area. Through dynamic musculoskeletal simulations of human walking and jumping, we demonstrate that recovered errors in fibre architecture characterisation have significant implications for quantitative predictions of in-vivo dynamics and muscle fibre function within a species. Furthermore, by applying data-subsampling simulations to comparisons of muscle function in humans and chimpanzees, we demonstrate that error magnitudes significantly impact both qualitative and quantitative assessment of muscle specialisation, potentially generating highly erroneous conclusions about the absolute and relative adaption of muscles across species and evolutionary transitions. Our findings have profound implications for how a broad diversity of research fields quantify muscle architecture and interpret muscle function.

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