Ying Z, Roy R R, Zhong H, Zdunowski S, Edgerton V R, Gomez-Pinilla F
Department of Physiological Science, University of California, Los Angeles, CA 90095-1527, USA.
Neuroscience. 2008 Sep 9;155(4):1070-8. doi: 10.1016/j.neuroscience.2008.06.057. Epub 2008 Jul 3.
Clinical evidence indicates that motor training facilitates functional recovery after a spinal cord injury (SCI). Brain-derived neurotrophic factor (BDNF) is a powerful synaptic facilitator and likely plays a key role in motor and sensory functions. Spinal cord hemisection decreases the levels of BDNF below the injury site, and exercise can counteract this decrease [Ying Z, Roy RR, Edgerton VR, Gomez-Pinilla F (2005) Exercise restores levels of neurotrophins and synaptic plasticity following spinal cord injury. Exp Neurol 193:411-419]. It is not clear, however, whether the exercise-induced increases in BDNF play a role in mediating the recovery of locomotion after a SCI. We performed a lateral cervical ( approximately C4) hemisection in adult rats. Seven days after hemisection, the BDNF inhibitor trkB IgG was injected into the cervical spinal cord below the lesion ( approximately C5-C6). Half of the rats were exposed to voluntary running wheels for 14 days. Locomotor ability was assessed by determining the symmetry between the contralateral (unaffected) vs. the ipsilateral (affected) forelimb at the most optimum treadmill speed for each rat. Sedentary and exercised rats with BDNF inhibition showed a higher level of asymmetry during the treadmill locomotion test than rats not treated with the BDNF inhibitor. In hemisected rats, exercise normalized the levels of molecules important for synaptic function, such as cyclic AMP response element binding protein (CREB) and synapsin I, in the ipsilateral cervical enlargement, whereas the BDNF blocker lessened these exercise-associated effects. The results indicate that BDNF levels play an important role in shaping the synaptic plasticity and in defining the level of recovery of locomotor performance after a SCI.
临床证据表明,运动训练有助于脊髓损伤(SCI)后的功能恢复。脑源性神经营养因子(BDNF)是一种强大的突触促进剂,可能在运动和感觉功能中起关键作用。脊髓半切会降低损伤部位以下的BDNF水平,而运动可以抵消这种降低[Ying Z,Roy RR,Edgerton VR,Gomez-Pinilla F(2005年)运动可恢复脊髓损伤后神经营养因子水平和突触可塑性。实验神经病学193:411 - 419]。然而,尚不清楚运动诱导的BDNF增加是否在介导SCI后运动恢复中起作用。我们对成年大鼠进行了颈外侧(约C4)半切。半切后7天,将BDNF抑制剂trkB IgG注入损伤部位以下的颈脊髓(约C5 - C6)。一半的大鼠暴露于自愿跑步轮14天。通过确定每只大鼠在最适宜跑步机速度下对侧(未受影响)与同侧(受影响)前肢之间的对称性来评估运动能力。与未用BDNF抑制剂治疗的大鼠相比,接受BDNF抑制的久坐不动和运动的大鼠在跑步机运动测试中表现出更高的不对称水平。在半切大鼠中,运动使同侧颈膨大处对突触功能重要的分子水平正常化,如环磷酸腺苷反应元件结合蛋白(CREB)和突触素I,而BDNF阻断剂减弱了这些与运动相关的作用。结果表明,BDNF水平在塑造突触可塑性和确定SCI后运动性能恢复水平方面起重要作用。