Ballak Sam B, Degens Hans, Busé-Pot Tinelies, de Haan Arnold, Jaspers Richard T
School of Healthcare Science, Cognitive Motor Function Research Group, Manchester Metropolitan University, Manchester, UK.
Age (Dordr). 2014;36(6):9726. doi: 10.1007/s11357-014-9726-0. Epub 2014 Nov 21.
The age-related decline in muscle function contributes to the movement limitations in daily life in old age. The age-related loss in muscle force is attributable to loss of myofibers, myofiber atrophy, and a reduction in specific force. The contribution of each of these determinants to muscle weakness in old age is, however, largely unknown. The objective of this study is to determine whether a loss in myofiber number, myofiber atrophy, and a reduction in specific muscle force contribute to the age-related loss of muscle force in 25-month-old mouse. Maximal isometric force of in situ m. plantaris of C57BL/6J male adult (9 months) and old (25 months) mice was determined and related to myofiber number, myofiber size, intramuscular connective tissue content, and proportion of denervated myofibers. Isometric maximal plantaris muscle force was 13 % lower in old than adult mice (0.97 ± 0.05 N vs. 0.84 ± 0.03 N; P < 0.05). M. plantaris mass of old mice was not significantly smaller than that of adult mice. There was also no significant myofiber atrophy or myofiber loss. Specific muscle force of old mice was 25 % lower than that of adult mice (0.55 ± 0.05 vs. 0.41 ± 0.03 N·mm(-2), P < 0.01). In addition, with age, the proportion of type IIB myofibers decreased (43.6 vs. 38.4 %, respectively), while the connective tissue content increased (11.6 vs. 16.4 %, respectively). The age-related reduction in maximal isometric plantaris muscle force in 25-month-old male C57BL/6J mice is mainly attributable to a reduction in specific force, which is for 5 % explicable by an age-related increase in connective tissue, rather than myofiber atrophy and myofiber loss.
与年龄相关的肌肉功能衰退导致老年人日常生活中的活动受限。与年龄相关的肌肉力量丧失归因于肌纤维的丢失、肌纤维萎缩以及比肌力的降低。然而,这些因素中每一个对老年人肌肉无力的影响在很大程度上尚不清楚。本研究的目的是确定肌纤维数量减少、肌纤维萎缩以及比肌力降低是否导致25月龄小鼠与年龄相关的肌肉力量丧失。测定了C57BL/6J雄性成年(9个月)和老年(25个月)小鼠原位跖肌的最大等长力,并将其与肌纤维数量、肌纤维大小、肌肉内结缔组织含量以及失神经支配肌纤维的比例相关联。老年小鼠的等长最大跖肌力量比成年小鼠低13%(0.97±0.05 N对0.84±0.03 N;P<0.05)。老年小鼠的跖肌质量并不显著小于成年小鼠。也没有明显的肌纤维萎缩或肌纤维丢失。老年小鼠的比肌力比成年小鼠低25%(0.55±0.05对0.41±0.03 N·mm(-2),P<0.01)。此外,随着年龄增长,IIB型肌纤维的比例下降(分别为43.6%和38.4%),而结缔组织含量增加(分别为11.6%和16.4%)。25月龄雄性C57BL/6J小鼠与年龄相关的最大等长跖肌力量降低主要归因于比肌力降低,其中5%可由结缔组织随年龄增长增加来解释,而非肌纤维萎缩和肌纤维丢失。