Rutkove Seward B, Chen Zsu-Zsu, Pandeya Sarbesh, Callegari Santiago, Mourey Tyler, Nagy Janice A, Nath Anjali K
Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Department of Endocrinology, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Biomedicines. 2023 Jul 7;11(7):1938. doi: 10.3390/biomedicines11071938.
Throughout a vertebrate organism's lifespan, skeletal muscle mass and function progressively decline. This age-related condition is termed sarcopenia. In humans, sarcopenia is associated with risk of falling, cardiovascular disease, and all-cause mortality. As the world population ages, projected to reach 2 billion older adults worldwide in 2050, the economic burden on the healthcare system is also projected to increase considerably. Currently, there are no pharmacological treatments for sarcopenia, and given the long-term nature of aging studies, high-throughput chemical screens are impractical in mammalian models. Zebrafish is a promising, up-and-coming vertebrate model in the field of sarcopenia that could fill this gap. Here, we developed a surface electrical impedance myography (sEIM) platform to assess skeletal muscle health, quantitatively and noninvasively, in adult zebrafish (young, aged, and genetic mutant animals). In aged zebrafish (85% lifespan) as compared to young zebrafish (20% lifespan), sEIM parameters (2 kHz phase angle, 2 kHz reactance, and 2 kHz resistance) robustly detected muscle atrophy ( < 0.000001, q = 0.000002; = 0.000004, q = 0.000006; = 0.000867, q = 0.000683, respectively). Moreover, these same measurements exhibited strong correlations with an established morphometric parameter of muscle atrophy (myofiber cross-sectional area), as determined by histological-based morphometric analysis (r = 0.831, = 2 × 10; r = 0.6959, = 2 × 10; and r = 0.7220; = 4 × 10, respectively). Finally, the genetic deletion of , an orphan G-protein coupled receptor (GPCR), exacerbated the atrophy of skeletal muscle in aged animals, as evidenced by both sEIM and histology. In conclusion, the data here show that surface EIM techniques can effectively discriminate between healthy young and sarcopenic aged muscle as well as the advanced atrophied muscle in the KO animals. Moreover, these studies show how EIM values correlate with cell size across the animals, making it potentially possible to utilize sEIM as a "virtual biopsy" in zebrafish to noninvasively assess myofiber atrophy, a valuable measure for muscle and gerontology research.
在整个脊椎动物的生命周期中,骨骼肌质量和功能会逐渐下降。这种与年龄相关的状况被称为肌肉减少症。在人类中,肌肉减少症与跌倒风险、心血管疾病以及全因死亡率相关。随着世界人口老龄化,预计到2050年全球老年人口将达到20亿,医疗保健系统的经济负担也预计会大幅增加。目前,尚无针对肌肉减少症的药物治疗方法,而且鉴于衰老研究的长期性,高通量化学筛选在哺乳动物模型中并不实用。斑马鱼是肌肉减少症领域一种有前景且崭露头角的脊椎动物模型,有望填补这一空白。在此,我们开发了一种表面电阻抗肌电图(sEIM)平台,用于定量和非侵入性地评估成年斑马鱼(年轻、年老和基因敲除动物)的骨骼肌健康状况。与年轻斑马鱼(约20%生命周期)相比,年老斑马鱼(约85%生命周期)的sEIM参数(2kHz相角、2kHz电抗和2kHz电阻)能有力地检测到肌肉萎缩(分别为<0.000001,q = 0.000002; = 0.000004,q = 0.000006; = 0.000867,q = 0.000683)。此外,这些测量结果与通过基于组织学的形态计量分析确定的肌肉萎缩既定形态计量参数(肌纤维横截面积)呈现出强相关性(分别为r = 0.831, = 2×10;r = 0.6959, = 2×10;以及r = 0.7220; = 4×10)。最后,孤儿G蛋白偶联受体(GPCR) 的基因缺失加剧了年老动物骨骼肌的萎缩,这在sEIM和组织学研究中均得到证实。总之,此处的数据表明表面EIM技术能够有效区分健康的年轻肌肉和患有肌肉减少症的年老肌肉,以及 基因敲除动物中晚期萎缩的肌肉。此外,这些研究还展示了EIM值如何与不同动物的细胞大小相关联,这使得利用sEIM作为斑马鱼的“虚拟活检”来非侵入性地评估肌纤维萎缩成为可能,这对肌肉和老年医学研究是一项有价值的测量方法。