Kim John T, Kasukonis Benjamin M, Brown Lemuel A, Washington Tyrone A, Wolchok Jeffrey C
Department of Biomedical Engineering, University of Arkansas, Fayetteville, AR 72701, United States.
Department of Health, Human Performance, and Recreation, College of Education and Health Professions, University of Arkansas, Fayetteville, AR, Fayetteville, AR 72701, United States.
Exp Gerontol. 2016 Oct;83:37-46. doi: 10.1016/j.exger.2016.07.008. Epub 2016 Jul 17.
Termed volumetric muscle loss (VML), the bulk loss of skeletal muscle tissue either through trauma or surgery overwhelms the capacity for repair, leading to the formation of non-contractile scar tissue. The myogenic potential, along with other factors that influence wound repair are known to decline with age. In order to develop effective treatment strategies for VML injuries that are effective across a broad range of patient populations, it is necessary to understand how the response to VML injury is affected by aging. Towards this end, this study was conducted to compare the response of young and aged animal groups to a lower extremity VML injury. Young (3months, n=12) and aged (18months, n=8) male Fischer 344 rats underwent surgical VML injury of the tibialis anterior muscle. Three months after VML injury it was found that young TA muscle was on average 16% heavier than aged muscle when no VML injury was performed and 25% heavier when comparing VML treated young and aged animals (p<0.0001, p<0.0001). Peak contractile force for both the young and aged groups was found to decrease significantly following VML injury, producing 65% and 59% of the contralateral limbs' peak force, respectively (p<0.0001). However, there were no differences found for peak contractile force based on age, suggesting that VML affects muscle's ability to repair, regardless of age. In this study, we used the ratio of collagen I to MyoD expression as a metric for fibrosis vs. myogenesis. Decreasing fiber cross-sectional area with advancing age (p<0.005) coupled with the ratio of collagen I to MyoD expression, which increased with age, supports the thought that regeneration is impaired in the aged population in favor of fibrosis (p=0.0241). This impairment is also exacerbated by the contribution of VML injury, where a 77-fold increase in the ratio of collagen I to MyoD was observed in the aged group (p<0.0002). The aged animal model described in this study provides a tool for investigators exploring not only the development of VML injury strategies but also the effect of aging on muscle regeneration.
骨骼肌组织因创伤或手术而大量损失,被称为容积性肌肉损失(VML),这超出了修复能力,导致形成无收缩能力的瘢痕组织。已知随着年龄增长,肌源性潜能以及其他影响伤口修复的因素会下降。为了制定对广泛患者群体都有效的VML损伤有效治疗策略,有必要了解衰老如何影响对VML损伤的反应。为此,本研究进行了比较年轻和老年动物组对下肢VML损伤的反应。年轻(3个月,n = 12)和老年(18个月,n = 8)雄性Fischer 344大鼠接受了胫骨前肌的手术VML损伤。VML损伤三个月后发现,在未进行VML损伤时,年轻的胫骨前肌平均比老年肌肉重16%,在比较接受VML治疗的年轻和老年动物时重25%(p<0.0001,p<0.0001)。发现年轻组和老年组的峰值收缩力在VML损伤后均显著下降,分别产生对侧肢体峰值力的65%和59%(p<0.0001)。然而,基于年龄未发现峰值收缩力存在差异,这表明VML会影响肌肉的修复能力,与年龄无关。在本研究中,我们使用I型胶原蛋白与MyoD表达的比率作为纤维化与肌生成的指标。随着年龄增长纤维横截面积减小(p<0.005),同时I型胶原蛋白与MyoD表达的比率随年龄增加,这支持了老年人群再生受损而有利于纤维化的观点(p = 0.0241)。VML损伤的影响也加剧了这种损伤,在老年组中观察到I型胶原蛋白与MyoD的比率增加了77倍(p<0.0002)。本研究中描述的老年动物模型为研究人员提供了一个工具,不仅可用于探索VML损伤策略的发展,还可用于研究衰老对肌肉再生的影响。