Deschenes M R, Maresh C M, Crivello J F, Armstrong L E, Kraemer W J, Covault J
Department of Physiology and Neurobiology, University of Connecticut, Storrs 06269-3042.
J Neurocytol. 1993 Aug;22(8):603-15. doi: 10.1007/BF01181487.
Little is known about the effects of exercise training on neuromuscular junction morphology in skeletal muscle. The objectives of this investigation were: 1) to determine if exercise training would elicit changes in neuromuscular junction morphology, 2) to determine if exercise training of different intensities would evoke specific changes in neuromuscular junction morphology, and 3) to determine whether changes in neuromuscular junction structure occur independently of changes in muscle fibre type and size. Twenty-four age and size matched male Sprague-Dawley rats were randomly assigned to three groups: high-intensity trained (HIT), low-intensity trained (LIT), or untrained. Neuromuscular junction morphology of the soleus muscle was determined via immunofluorescent staining. Presynaptic acetylcholine vesicles were visualized with SV-2 antibody in conjunction with fluorescein isothiocyanate labelled secondary secondary antibody. Postsynaptic acetylcholine receptors were identified with rhodamine labelled alpha-bungarotoxin. Laser scanning microscopy was used to produce images of synapses, which were used to quantitate the following: total area of SV-2 and alpha-bungarotoxin staining, density of acetylcholine vesicles and receptors, structural complexity, and synaptic coupling. To visualize nerve terminal branching, a smaller number of neuromuscular junctions were stained with C-2 antibody, which reacts with a neurofilament epitope, in conjunction with fluorescein isothiocyanate labelled secondary antibody. Total length of branching, number of branches, average length of branches, and ratio of secondary to primary branches per neuromuscular junction were determined. Citrate synthase activity, fibre type composition and fibre cross-sectional areas of the soleus muscle were assessed to determine the presence of a training effect in that muscle. Results indicate that training did induce hypertrophy of the neuromuscular junction that was independent of muscle hypertrophy. Although the HIT and LIT groups exhibited similar hypertrophic responses of the neuromuscular junction, the HIT group displayed more dispersed synapses than the LIT group. Neither exercise training program, however, resulted in altered densities of acetylcholine vesicles or receptors, nor did training significantly change synaptic coupling. Nerve terminal branching was also affected by exercise training. Neuromuscular junctions from the HIT group demonstrated a greater total length of branching, average length per branch, and number of finer, or secondary, branches than those of the LIT group.
关于运动训练对骨骼肌神经肌肉接头形态的影响,人们了解甚少。本研究的目的是:1)确定运动训练是否会引起神经肌肉接头形态的变化;2)确定不同强度的运动训练是否会引发神经肌肉接头形态的特定变化;3)确定神经肌肉接头结构的变化是否独立于肌纤维类型和大小的变化。将24只年龄和体型匹配的雄性Sprague-Dawley大鼠随机分为三组:高强度训练组(HIT)、低强度训练组(LIT)或未训练组。通过免疫荧光染色确定比目鱼肌的神经肌肉接头形态。用SV-2抗体结合异硫氰酸荧光素标记的二抗来观察突触前乙酰胆碱囊泡。用罗丹明标记的α-银环蛇毒素来识别突触后乙酰胆碱受体。使用激光扫描显微镜生成突触图像,用于量化以下指标:SV-2和α-银环蛇毒素染色的总面积、乙酰胆碱囊泡和受体的密度、结构复杂性以及突触耦合。为了观察神经末梢分支,用与神经丝表位反应的C-2抗体结合异硫氰酸荧光素标记的二抗对少量神经肌肉接头进行染色。确定每个神经肌肉接头的分支总长度、分支数量、平均分支长度以及二级分支与一级分支的比例。评估比目鱼肌的柠檬酸合酶活性、纤维类型组成和纤维横截面积,以确定该肌肉中是否存在训练效果。结果表明,训练确实诱导了神经肌肉接头的肥大,且这种肥大与肌肉肥大无关。尽管HIT组和LIT组在神经肌肉接头肥大反应方面相似,但HIT组的突触比LIT组更分散。然而,两个运动训练方案均未导致乙酰胆碱囊泡或受体密度的改变,训练也未显著改变突触耦合。运动训练也影响神经末梢分支。HIT组的神经肌肉接头比LIT组表现出更长的分支总长度、平均每个分支的长度以及更多更细的或二级分支数量。