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中文摘要
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描述(由申请人提供):骨骼肌停用是导致身体残疾的重要因素。废用在老年人中更常见,他们更容易受到其衰弱效应的影响,因为他们的生理储备减少。尽管有这些事实,但在这一人群中,停用促进骨骼肌收缩功能障碍的机制在很大程度上仍然不确定。因此,我们建议系统地测试作为收缩功能障碍基础的单一肌肉纤维结构和功能的改变。以慢性肌肉停用为特征的老年人将与活动水平正常的精心匹配的对照组进行比较。此后,患有慢性废用的老年人将接受运动干预,以补救肌肉废用。我们假设,肌肉停用损害收缩功能,部分是通过肌球蛋白动力学、肌丝蛋白含量和肌丝格子的机械性能的改变,运动康复可以抵消这些缺陷。目的1将在病例和对照中研究停用对单个肌肉纤维的机械、动力学和结构特性以及分子组成的影响。目的2将研究通过运动训练增加老年慢性停用患者的肌肉使用量如何影响肌肉纤维的力学、动力学和结构特性以及分子组成。我们实验室的创新首次使在人类肌球蛋白-肌动蛋白跨桥水平上评估肌肉功能成为可能。结合其他力学、生化和解剖学测量,这些翻译研究将首次全面评估肌肉停用改变老年人骨骼肌结构和收缩功能的细胞和分子机制。这些知识可以通过调整这些方法来解决特定的分子缺陷,从而帮助开发和完善残疾的预防和纠正疗法。 公共卫生相关性:骨骼肌停用是导致老年人残疾的一个重要因素。尽管老年人更有可能经历废用,并且缺乏生理储备来缓冲其有害影响,但废用相关肌肉收缩功能障碍背后的细胞和分子机制在很大程度上仍未得到研究。从拟议的研究中获得的知识将通过调整这些方法来解决特定的细胞和分子缺陷,从而帮助开发和完善针对残疾的预防性和纠正性临床疗法。
英文摘要
DESCRIPTION (provided by applicant): Skeletal muscle disuse is an important contributing factor to physical disability. Disuse is more frequent in the elderly and they are more susceptible to its debilitating effects because of their diminished physiological reserve. Despite these facts, the mechanisms whereby disuse promotes skeletal muscle contractile dysfunction in this population remain largely undetermined. Therefore, we propose to systematically test for modifications of single muscle fiber structure and function that underlie contractile dysfunction. Elderly individuals characterized by chronic muscle disuse will be compared to carefully-matched controls with normal activity levels. Thereafter, elderly with chronic disuse will undergo an exercise intervention to remediate muscle disuse. We hypothesize that muscle disuse impairs contractile function, in part, through alterations in myosin kinetics, myofilament protein content and the mechanical properties of the myofilament lattice and that exercise rehabilitation will counteract these deficits. Aim 1 will examine the effect of disuse on mechanical, kinetic and structural properties and molecular composition of single muscle fibers in cases and controls. Aim 2 will investigate how increasing muscle use in elderly with chronic disuse via exercise training affects muscle fiber mechanical, kinetic and structural properties and molecular composition. Innovations in our laboratories have enabled assessment of muscle function at the level of the myosin-actin cross-bridge in humans for the first time. In combination with other mechanical, biochemical and anatomical measurements, these translational studies will provide the first comprehensive evaluation of the cellular and molecular mechanisms through which muscle disuse alters skeletal muscle structure and contractile function in elderly humans. This knowledge can assist in the development and refinement of preventative and corrective therapies for disability by tailoring these approaches to address specific molecular defects. PUBLIC HEALTH RELEVANCE: Skeletal muscle disuse is an important contributing factor to disability in the elderly. Despite the fact that elderly are more likely to experience disuse and lack the physiological reserve to buffer its detrimental effects, the cellular and molecular mechanisms that underlie disuse-related muscle contractile dysfunction remain largely unstudied. Knowledge gained from the proposed studies will assist in the development and refinement of preventative and corrective clinical therapies for disability by tailoring these approaches to address specific cellular and molecular defects.
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Skeletal Muscle Atrophy and Dysfunction in Human Cancer
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Skeletal Muscle Atrophy and Dysfunction Following Total Knee Arthroplasty
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