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Biochemical and structural basis of the passive mechanical properties of whole skeletal muscle

期刊

JOURNAL OF PHYSIOLOGY-LONDON
卷 599, 期 16, 页码 3809-3823

出版社

WILEY
DOI: 10.1113/JP280867

关键词

extracellular matrix; muscle fibre bundles; muscle mechanics; muscle scaling; perimysium; sarcomere length

资金

  1. National Institutes of Health [R01AR057393, R24HD050837, P30AR061303]
  2. Department of Veterans Affairs [101RX000670, I01RX002462]
  3. United States Department of Veterans Affairs Rehabilitation RD Service [IK6 RX003351]

向作者/读者索取更多资源

Passive mechanical properties of whole skeletal muscle are not as well understood as active mechanical properties, mainly due to uncertainties in load bearing structures and lack of established standards for mechanical measurements. Evidence suggests that titin bears most of the passive load within single muscle cells, while extracellular matrix bears the major part of the load at larger scales. Definitions of muscle passive properties such as stress, strain, modulus and stiffness can vary relative to different reference parameters, making it difficult to fully understand and model whole muscle passive mechanical properties.
Passive mechanical properties of whole skeletal muscle are not as well understood as active mechanical properties. Both the structural basis for passive mechanical properties and the properties themselves are challenging to determine because it is not clear which structures within skeletal muscle actually bear passive loads and there are not established standards by which to make mechanical measurements. Evidence suggests that titin bears the majority of the passive load within the single muscle cell. However, at larger scales, such as fascicles and muscles, there is emerging evidence that the extracellular matrix bears the major part of the load. Complicating the ability to quantify and compare across size scales, muscles and species, definitions of muscle passive properties such as stress, strain, modulus and stiffness can be made relative to many reference parameters. These uncertainties make a full understanding of whole muscle passive mechanical properties and modelling these properties very difficult. Future studies defining the specific load bearing structures and their composition and organization are required to fully understand passive mechanics of the whole muscle and develop therapies to treat disorders in which passive muscle properties are altered such as muscular dystrophy, traumatic laceration, and contracture due to upper motor neuron lesion as seen in spinal cord injury, stroke and cerebral palsy.

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