Zhou Yu, Lovell Daniel, Bethea Maigen, Wang Zhan, Christ George J, Soker Shay, Criswell Tracy
Wake Forest Institute for Regenerative Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Wake Forest Institute for Regenerative Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Am J Pathol. 2014 Aug;184(8):2225-36. doi: 10.1016/j.ajpath.2014.03.018. Epub 2014 Jun 6.
Declining skeletal muscle function, due to injury and aging (sarcopenia), results in a significantly decreased quality of life and is a major cause of disability in the United States. Studies examining recovery from muscle injury in models of older animals principally used insults that primarily affect only the myofibers without affecting the muscle tissue microenvironment. This type of injury does not adequately represent the full extent of tissue damage observed in older humans, which encompasses injury not only to the muscle fibers, but also to the surrounding tissue components, such as the vasculature and nerves. Previously, we described a novel rat model of compression-induced muscle injury that results in multicomponent injury to the muscle and adequately mimics compartment syndrome injuries seen in patients. Herein, we characterized tissue regeneration in young, adult, and aged rats after compartment syndrome injury. We observed significant differences between the regeneration process in the different aged rats that involved muscle function, tissue anatomical features, neovascularization, and innervation. Compared to young rats, adult rats had delayed functional recovery, whereas the aged rats were deficient in their regenerative capacity. Age-dependent changes in both the ability to restore the contractile apparatus and myogenesis are important, and must be taken into consideration when designing therapies for the treatment of muscle injury.
由于损伤和衰老(肌肉减少症)导致的骨骼肌功能衰退,会显著降低生活质量,并且是美国残疾的主要原因。在老年动物模型中研究肌肉损伤恢复情况的研究,主要使用的损伤方式主要仅影响肌纤维,而不影响肌肉组织微环境。这种损伤类型不能充分代表在老年人中观察到的组织损伤的全部程度,其中不仅包括肌肉纤维的损伤,还包括周围组织成分,如脉管系统和神经的损伤。此前,我们描述了一种新型的压迫性肌肉损伤大鼠模型,该模型会导致肌肉多成分损伤,并充分模拟患者中出现的骨筋膜室综合征损伤。在此,我们对骨筋膜室综合征损伤后年轻、成年和老年大鼠的组织再生进行了表征。我们观察到不同年龄大鼠的再生过程在肌肉功能、组织解剖特征、新生血管形成和神经支配方面存在显著差异。与年轻大鼠相比,成年大鼠的功能恢复延迟,而老年大鼠的再生能力不足。恢复收缩装置的能力和肌生成的年龄依赖性变化都很重要,在设计肌肉损伤治疗方案时必须予以考虑。