Mechanisms leading to restoration of muscle size with exercise and transplantation after spinal cord injury
- 1 December 2000
- journal article
- research article
- Published by American Physiological Society in American Journal of Physiology-Cell Physiology
- Vol. 279 (6) , C1677-C1684
- https://doi.org/10.1152/ajpcell.2000.279.6.c1677
Abstract
We have shown that cycling exercise combined with fetal spinal cord transplantation restored muscle mass reduced as a result of complete transection of the spinal cord. In this study, mechanisms whereby this combined intervention increased the size of atrophied soleus and plantaris muscles were investigated. Rats were divided into five groups (n = 4, per group): control, nontransected; spinal cord transected at T10 for 8 wk (Tx); spinal cord transected for 8 wk and exercised for the last 4 wk (TxEx); spinal cord transected for 8 wk with transplantation of fetal spinal cord tissue into the lesion site 4 wk prior to death (TxTp); and spinal cord transected for 8 wk, exercised for the last 4 wk combined with transplantation 4 wk prior to death (TxExTp). Tx soleus and plantaris muscles were decreased in size compared with control. Exercise and transplantation alone did not restore muscle size in soleus, but exercise alone minimized atrophy in plantaris. However, the combination of exercise and transplantation resulted in a significant increase in muscle size in soleus and plantaris compared with transection alone. Furthermore, myofiber nuclear number of soleus was decreased by 40% in Tx and was not affected in TxEx or TxTp but was restored in TxExTp. A strong correlation (r = 0.85) between myofiber cross-sectional area and myofiber nuclear number was observed in soleus, but not in plantaris muscle, in which myonuclear number did not change with any of the experimental manipulations. 5′-Bromo-2′-deoxyuridine-positive nuclei inside the myofiber membrane were observed in TxExTp soleus muscles, indicating that satellite cells had divided and subsequently fused into myofibers, contributing to the increase in myonuclear number. The increase in satellite cell activity did not appear to be controlled by the insulin-like growth factors (IGF), as IGF-I and IGF-II mRNA abundance was decreased in Tx soleus and plantaris, and was not restored with the interventions. These results indicate that, following a relatively long postinjury interval, exercise and transplantation combined restore muscle size. Satellite cell fusion and restoration of myofiber nuclear number contributed to increased muscle size in the soleus, but not in plantaris, suggesting that cellular mechanisms regulating muscle size differ between muscles with different fiber type composition.Keywords
This publication has 50 references indexed in Scilit:
- Two Experimental Strategies to Restore Muscle Mass in Adult Rats Following Spinal Cord InjuryNeurorehabilitation and Neural Repair, 1999
- Angiogenic and inflammatory responses following skeletal muscle injury are altered by immune neutralization of endogenous basic fibroblast growth factor, insulin-like growth factor-1 and transforming growth factor-β1Journal of Neuroimmunology, 1996
- Spinal Cord Repair in Adult Paraplegic Rats: Partial Restoration of Hind Limb FunctionScience, 1996
- Insulinlike growth factor gene expression in rat muscle during reinnervationMuscle & Nerve, 1995
- A quantitative study of satellite cells and myonuclei in stretched avian slow tonic muscleThe Anatomical Record, 1992
- Transplantation of fetal spinal cord tissue into the chronically injured adult rat spinal cordJournal of Comparative Neurology, 1988
- Fiber type and fiber size changes in selected thigh muscles six months after low thoracic spinal cord transection in adult cats: Exercise effectsExperimental Neurology, 1986
- Morphometric analyses on the muscles of exercise trained and untrained dogsJournal of Anatomy, 1983
- The distribution of satellite cells and their relationship to specific fiber types in soleus and extensor digitorum longus musclesThe Anatomical Record, 1982
- Structure and variation of human ribosomal DNA: molecular analysis of cloned fragmentsGene, 1981