Rice Kevin M, Linderman Jon K, Kinnard Randy S, Blough Eric R
Department of Biological Sciences, Marshall University, Huntington, WV 25755-1090, USA.
Biogerontology. 2005;6(5):335-43. doi: 10.1007/s10522-005-4808-0.
Sarcopenia, characterized by profound muscle atrophy and the loss of contractile function, contributes significantly to the development of frailty and functional impairment in older age. Although present in aging humans, rat models have failed to clearly demonstrate a similar degree of this age-associated loss of muscle mass and function. This investigation compared two models of rats raised specifically for aging studies, the Fischer 344/NNiaHSd (F344/N) and the Fischer 344/NNiaHSd X Brown Norway/BiNia (F344/NXBN), and sought to determine which model provides the most accurate representation of human sarcopenia. We found that aging had no effect on F344/N muscle mass or contractile function in the extensor digitorum longus (EDL) and soleus (SOL). Conversely, in the F344/NXBN model, aging was found to decrease EDL and SOL mass and contractile function. These changes were sufficient to satisfy the proposed criteria for the diagnosis of human sarcopenia based upon muscle mass and contractile function. Results indicate that the F344/NXBN provides a better model of the alterations seen in aging human muscle than the F344/N rat model.
肌肉减少症,其特征为严重的肌肉萎缩和收缩功能丧失,在老年人衰弱和功能障碍的发展中起重要作用。虽然在老年人类中存在,但大鼠模型未能清楚地证明这种与年龄相关的肌肉质量和功能丧失的相似程度。本研究比较了两种专门为衰老研究培育的大鼠模型,即Fischer 344/NNiaHSd(F344/N)和Fischer 344/NNiaHSd×Brown Norway/BiNia(F344/NXBN),并试图确定哪种模型能最准确地反映人类肌肉减少症。我们发现衰老对F344/N大鼠的趾长伸肌(EDL)和比目鱼肌(SOL)的肌肉质量或收缩功能没有影响。相反,在F344/NXBN模型中,衰老导致EDL和SOL的质量及收缩功能下降。这些变化足以满足基于肌肉质量和收缩功能诊断人类肌肉减少症的提议标准。结果表明,与F344/N大鼠模型相比,F344/NXBN能更好地模拟衰老人类肌肉中出现的变化。