Yeo Hyo-Seong, Lim Jae-Young, Ahn Na-Young
Department of Rehabilitation Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Department of Physical Education, College of Physical Education, Keimyung University, Daegu, Korea.
Ann Geriatr Med Res. 2020 Dec;24(4):305-312. doi: 10.4235/agmr.20.0077. Epub 2020 Dec 29.
This study explored the effects of aging on the expression of angiogenic and muscle protein synthesis factors, as well as the number of satellite cells affecting sarcopenia in naturally aged rat skeletal muscles.
We divided 16 Sprague-Dawley rats into young (12 weeks old, n=8) and old (24 months old, n=8) groups and compared muscle and body weight (BW) between them. We also analyzed the expression levels of angiogenic and muscle growth proteins in soleus (slow-twitch) and extensor digitorum longus (EDL; fast-twitch) muscles by western blotting and assessed the number of skeletal muscle satellite cells and myonuclei and mean fiber cross-sectional area (CSA) using by immunofluorescence staining.
EDL/BW was significantly lower in old rats than in young rats (p=0.002). The vascular endothelial growth factor level in soleus muscles was significantly lower in old rats than in young rats (p=0.001). Hypoxia-inducible factor 1-alpha and fetal liver kinase 1 levels in EDL muscles were lower in old rats than in young rats (p=0.001). The mammalian target of rapamycin (mTOR), p70S6K, and 4E-BP1 levels were significantly lower in the soleus muscles of old rats than in those of young rats (p<0.01). Similarly, insulin growth factor-1, Akt, mTOR, and p70S6K levels were significantly lower in EDL muscles of old rats than in those of young rats (p<0.01). Additionally, myonuclei/fiber, Pax7/fiber, and mean fiber CSAs in both muscle types were significantly lower in old rats than in young rats (p<0.01).
Conclusion These data suggest different regulation of indices of angiogenic and muscle growth with aging in different muscle types.
本研究探讨衰老对血管生成和肌肉蛋白合成因子表达的影响,以及对自然衰老大鼠骨骼肌中影响肌肉减少症的卫星细胞数量的影响。
我们将16只Sprague-Dawley大鼠分为年轻组(12周龄,n = 8)和老年组(24月龄,n = 8),并比较两组之间的肌肉和体重(BW)。我们还通过蛋白质印迹法分析比目鱼肌(慢肌)和趾长伸肌(EDL;快肌)中血管生成和肌肉生长蛋白的表达水平,并使用免疫荧光染色评估骨骼肌卫星细胞和肌核的数量以及平均纤维横截面积(CSA)。
老年大鼠的EDL/BW显著低于年轻大鼠(p = 0.002)。老年大鼠比目鱼肌中的血管内皮生长因子水平显著低于年轻大鼠(p = 0.001)。老年大鼠EDL肌肉中的缺氧诱导因子1-α和胎儿肝激酶1水平低于年轻大鼠(p = 0.001)。老年大鼠比目鱼肌中雷帕霉素靶蛋白(mTOR)、p70S6K和4E-BP1水平显著低于年轻大鼠(p<0.01)。同样,老年大鼠EDL肌肉中的胰岛素生长因子-1、Akt、mTOR和p70S6K水平显著低于年轻大鼠(p<0.01)。此外,老年大鼠两种肌肉类型中的肌核/纤维、Pax7/纤维和平均纤维CSA均显著低于年轻大鼠(p<0.01)。
这些数据表明不同肌肉类型中血管生成和肌肉生长指标随衰老的调节方式不同。