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首页> 外文期刊>Journal of Biomechanics >Effects of non-contractile inclusions on mechanical performance of skeletal muscle
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Effects of non-contractile inclusions on mechanical performance of skeletal muscle

机译:非收缩夹杂物对骨骼肌机械性能的影响

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摘要

Glycogen storage disease 11 is an inherited progressive muscular disease in which the lack of functional acid 1-4 alpha-glucosidase results in the accumulation of lysosomal glycogen. In the present study, we examine the effect of these non-contractile inclusions on the mechanical performance of skeletal muscle. To this end, force developed in an isometrically contracting slice of a muscle was calculated with a finite element model. Force was calculated at several inclusion densities and distributions and compared to muscle lacking inclusions. Furthermore, ankle dorsal flexor torque was measured in situ of alpha-glucosidase null mice of 6 months of age and unaffected litter mates as was inclusion density in the dorsal flexor muscles.The calculated force loss was shown to be almost exclusively dependent on the inclusion density and less on the type of inclusion distribution. The force loss predicted by the model (6%) on the basis of measured inclusion density (3.3%) corresponded to the loss in mass-normalized strength in these mice measured in situ (7%). Therefore, we conclude that the mechanical interaction between the non-contractile inclusions and the nearby myofibrils is a key factor in the loss of force per unit muscle mass during early stages of GSD II in mice. As glycogen accumulation reaches higher levels in humans, it is highly probable that the impact of this mechanical interaction is even more severe in human skeletal muscle. (c) 2004 Elsevier Ltd. All rights reserved.
机译:糖原储存疾病11是一种遗传性进行性肌肉疾病,其中缺乏功能性酸1-4α-葡萄糖苷酶会导致溶酶体糖原的积累。在本研究中,我们检查了这些非收缩性包裹体对骨骼肌机械性能的影响。为此,用有限元模型计算了在肌肉等距收缩的切片中产生的力。在几个夹杂物密度和分布处计算力,并与缺少夹杂物的肌肉进行比较。此外,对6个月大的α-葡萄糖苷酶无效小鼠和未患病的同伴进行了踝背屈扭矩的原位测量,以及背屈肌中的包裹物密度,计算得出的力损失几乎完全取决于包裹物密度而关于夹杂物分布的类型则更少。在测得的夹杂物​​密度(3.3%)的基础上,模型预测的力损失(6%)对应于这些在原位测量的小鼠的质量归一化强度损失(7%)。因此,我们得出结论,非收缩性包涵体和附近的肌原纤维之间的机械相互作用是小鼠GSD II早期每单位肌肉质量力量损失的关键因素。随着人体中糖原积累达到更高的水平,这种机械相互作用的影响很有可能在人体骨骼肌中更为严重。 (c)2004 Elsevier Ltd.保留所有权利。

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