Effect of passive movement on hind limb motor function and skeletal muscle in rats with spinal cord injury
YANG Xuan, LI Xian, ZHANG Peng, LIN Sen, YU Hong-yu
Chinese Journal of Clinical Anatomy ›› 2018, Vol. 36 ›› Issue (3) : 299-303.
Effect of passive movement on hind limb motor function and skeletal muscle in rats with spinal cord injury
Objective To observe the effect of passive motion on the recovery of the motor function of the hind limbs and the improvement of the skeletal muscle atrophy in the rats with spinal cord injury(SCI), and to explore the effect of brain derived neurotrophic factor (BDNF) on the functional recovery of passive motion and the treatment of muscular atrophy. Methods 36 healthy adult female SD rats were randomly divided into a sham operation group, a control group (no exercise), and a passive exercise group (1 week after injury, passive motion, for 4 weeks). A modified Allen’s method was used to establish the spinal cord injury model. The rats' motor function was detected by the Basso-Beattie-Bresnahan (BBB) behavior score of rats at 1 d, 1, 2, 3, 4, 5 week after SCI. HE staining was used to compare the pathological changes of spinal cord tissue in each group, and the cross section area, diameter and morphology of the gastrocnemius muscle in the hind limbs of the rats were observed. The wet weight of gastrocnemius, weight, and muscle weight / weight were measured. The expression of BDNF in the gastrocnemius muscle was detected by Western blots. Results The motor function of passive movement group was significantly higher than the control group (P<0.05). After SCI 5 weeks, the spinal cord tissue of the control group and passive movement group lost normal morphology, the number of neurons were reduced, a large number of cysts were formed in lesion area, but passive movement group were better than the control group when it came to the above mentioned parameters. The gastrocnemius muscle weight, muscle weight / body weight, cross-sectional area and diameter were smaller in the control group. Therefore the passive movement group improved the situation of muscle atrophy (P<0.05). Compared with sham operation group, the expression of BDNF in control group and passive movement group gastrocnemius muscle were increased (P<0.05), and it was higher in gastrocnemius muscle of the passive movement group than that of the control group (P<0.05). Conclusion Passive motion might promote the recovery of motor function and improve the atrophy of denervated muscle by increasing BDNF in the gastrocnemius muscle after SCI.
Spinal cord injury; Passive motion; Muscular atrophy; Brain derived neurotrophic factor;  / Rat
[1] Mcdonald JW, Sadowsky C. Spinal-cord injury[J]. Lancet, 2002, 359(9304): 417-425.
[2] Herman PE, Papatheodorou A, Bryant SA, et al. Highly conserved molecular pathways, including Wnt signaling, promote functional recovery from spinal cord injury in lampreys[J]. Sci Rep, 2018, 8 (1): 742.
[3] 孙嘉利, 单守勤, 黄美贤,等. 现代战创伤致脊髓损伤患者的三维步态分析[J]. 中国临床解剖学杂志, 2015, 33(2): 209-212.
[4] 唐丹, 刘四文, 邓小倩,等. 重心移动式截瘫步行矫形器对胸腰段脊髓损伤患者的疗效分析[J]. 中国临床解剖学杂志, 2017, 35(2): 224-227.
[5] Wei ZJ, Zhou XH, Fan BY, et al. Proteomic and bioinformatic analyses of spinal cord injury-induced skeletal muscle atrophy in rats[J]. Mol Med Rep, 2016, 14(1): 165-174.
[6] Gorgey AS, Dudley GA. Skeletal muscle atrophy and increased intramuscular fat after incomplete spinal cord injury[J]. Spinal Cord, 2007, 45(4): 304-309.
[7] Apostolopoulos N, Metsios GS, Flouris AD, et al. The relevance of stretch intensity and position-a systematic review[J]. Fron Psychol, 2015, 6:1128.
[8] Katalinic OM, Harvey LA, Herbert RD, et al. Stretch for the treatment and prevention of contractures[J]. Cochrane Database Syst Rev, 2010, 8(9): CD007455.
[9] Williams PE. Use of intermittent stretch in the prevention of serial sarcomere loss in immobilised muscle[J]. Ann Rheum Dis, 1990, 49(5): 316-317.
[10]Kinney MC, Dayanidhi S, Dykstra PB, et al. Reduced skeletal muscle satellite cell number alters muscle morphology after chronic stretch but allows limited serial sarcomere addition[J]. Muscle Nerve, 2017, 55(3): 384-392.
[11]Garraway SM, Huie JR. Spinal plasticity and behavior: BDNF-induced neuromodulation in uninjured and injured spinal cord[J]. Neural Plast, 2016, 2016: 9857201.
[12]卢虎英, 徐基民, 刘兰群,等. 减重步行训练结合督脉电针对脊髓损伤大鼠运动功能和脑源性神经营养因子的影响[J]. 中国康复医学杂志, 2013, 28(6): 553-557.
[13]Ilha J,da Cunha NB,Jaeger M, et al. Treadmill step training-induced adaptive muscular plasticity in a chronic paraplegia model[J]. Neurosci Lett,2011, 492(3): 170-174.
[14]丁晓晶, 王瑾, 王红星, 等. 减重平板训练对脊髓损伤大鼠运动功能及远端脊髓形态学的影响[J]. 中国康复医学杂志, 2011, 26(3): 210-214
[15]Jung SY, Kim DY, Yune TY, et al. Treadmill exercise reduces spinal cord injury-induced apoptosis by activating the PI3K/Akt pathway in rats[J]. Exp Ther Md, 2014, 7(3): 587-593.
[16]王元元, 洪毅, 王雪飞. 脊髓损伤大鼠远端神经元及骨骼肌的变化[J]. 中国组织工程研究, 2014, 18(33): 5323-5328.
[17]Higashino K, Matsuura T, Suganuma K, et al. Early changes in muscle atrophy and muscle fiber type conversion after spinal cord transection and peripheral nerve transection in rats[J]. J NeuroEng and Rehabil, 2013, 10: 46.
[18]韩利军, 梁炳生, 王乐,等. 失神经骨骼肌萎缩中泛素蛋白连接酶Murf1和核转录因子NF-κB表达与被动运动干预[J]. 中国组织工程研究与临床康复, 2010, 14(24): 4435-4438.
[19]刘泽远, 张文苹, 黄强开,等. 被动运动干预对大鼠失神经萎缩骨骼肌中miRNA-1表达和成肌细胞分化的影响[J]. 中国修复重建外科杂志, 2016(5): 612-618.
[20]Houle JD, Cté MP. Axon regeneration and exercise-dependent plasticity after spinal cord injury[J]. Ann N Y Acad Sci, 2013, 1279: 154-163.
[21]阚世廉, 李桂石, 詹海华,等. 大鼠周围神经移植修复后脊髓前角运动神经元变化的动态观察[J]. 中国临床解剖学杂志, 2016, 34(5): 534-539.
[22]Dupont-Versteegden EE, Houlé JD, Dennis RA, et al. Exercise-induced gene expression in soleus muscle is dependent on time after spinal cord injury in rats[J]. Muscle Nerve, 2004, 29(1): 73-81.
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