Department of Neurological Surgery, Thomas Jefferson University, 909 Walnut Street, Philadelphia, PA 19107, USA.
Neuroscience. 2010 Oct 27;170(3):929-41. doi: 10.1016/j.neuroscience.2010.07.041. Epub 2010 Jul 29.
Epidemiological studies have demonstrated a relationship between advancing age and susceptibility to risk factors for median neuropathies and musculoskeletal disorders. In this study, we determined if performance of a voluntary reaching task by aged rats induced sensorimotor declines, median nerve dysfunction and increased inflammatory cytokines in peripheral nerves, muscle and spinal cord neurons. Aged (14 mon) rats were trained for 15 min/day for 4 weeks to learn a high repetition, low force (HRLF) task (19 reaches/min; 15% maximum pulling force). Aged task rats performed the task for 2 h/day, 3 days/wk, for 12 weeks (until they were 18 mon of age). No behavioral changes were detected in normal controls (NC) or food-restricted controls (FR C) as they aged. However, grip strength declined in HRLF rats in weeks 6-12 (P<0.01 each) and 12-week trained-only rats (TR; P<0.05), compared to NC. Mechanical hypersensitivity was present in weeks 9 and 12 HRLF reach limb forepaws (P<0.01 and P<0.05, respectively), and 12-week HRLF support limb forepaws (P<0.01) and hindpaws (P=0.03), compared to NC. By week 12, median nerve conduction velocity declined 23%, bilaterally, in HRLF (P<0.001 each), and 13% in TR (P<0.05), compared to NC. Tumor necrosis factor alpha (TNFα) increased in 12-week HRLF muscle (P=0.005), median nerve (P<0.01), and neurons in superficial lamina of HRLF cervical spinal cords (P<0.01), compared to NC. interleukin 1 beta (IL1β) also increased in superficial lamina neurons (P<0.01). Loss of grip strength was correlated with median nerve conduction slowing (r=0.70) as well as increased nerve and muscle TNFα (r=-0.38 and r=-0.41, respectively); decrease in forepaw withdrawal thresholds was correlated with median nerve conduction slowing (r=0.81), increased nerve TNFα (r=-0.59), and increased TNFα and IL1β in neurons in spinal cord dorsal horns (r=-0.52 and r=-0.47, respectively). Thus, aged rats performing a repetitive task exhibited sensorimotor declines that were associated with decreased median nerve conduction, and increased pro-inflammatory cytokines in the median nerve and cervical spinal cord neurons.
流行病学研究表明,年龄的增长与正中神经病变和肌肉骨骼疾病的危险因素易感性之间存在关系。在这项研究中,我们确定了老年大鼠进行自愿伸展任务是否会导致感觉运动能力下降、正中神经功能障碍以及外周神经、肌肉和脊髓神经元中炎症细胞因子的增加。老年(14 个月)大鼠接受了 4 周的 15 分钟/天的训练,以学习高重复、低力(HRLF)任务(19 次/分钟;15%最大拉力)。老年任务大鼠每天进行 2 小时/天,每周 3 天,共 12 周(直到它们 18 个月大)。正常对照组(NC)或限食对照组(FR C)随着年龄的增长没有检测到行为变化。然而,HRLF 大鼠在第 6-12 周(P<0.01)和仅训练 12 周的大鼠(TR;P<0.05)的握力下降,与 NC 相比。HRLF 伸展前爪的机械性超敏反应在第 9 周和第 12 周(分别为 P<0.01 和 P<0.05),以及第 12 周的 HRLF 支撑前爪(P<0.01)和后爪(P=0.03)存在,与 NC 相比。到第 12 周,HRLF 双侧正中神经传导速度下降 23%(P<0.001),TR 下降 13%(P<0.05),与 NC 相比。肿瘤坏死因子-α(TNFα)在 12 周的 HRLF 肌肉(P=0.005)、正中神经(P<0.01)和 HRLF 颈脊髓浅层神经元中增加(P<0.01),与 NC 相比。白细胞介素 1β(IL1β)也在浅层神经元中增加(P<0.01)。握力下降与正中神经传导速度减慢(r=0.70)以及神经和肌肉 TNFα 增加(r=-0.38 和 r=-0.41)相关;前爪撤回阈值的降低与正中神经传导速度减慢(r=0.81)、神经 TNFα 增加(r=-0.59)以及脊髓背角神经元中 TNFα 和 IL1β 的增加(r=-0.52 和 r=-0.47)相关。因此,进行重复性任务的老年大鼠表现出感觉运动能力下降,与正中神经传导降低以及正中神经和颈脊髓神经元中促炎细胞因子增加有关。