muscular activation

肌肉激活
  • 文章类型: Journal Article
    背景:据报道,帕金森病患者的姿势控制不佳,这可以通过与反重力肌肉相关的肌肉激活模式的变化来解释。这项研究旨在测量在个人平衡任务期间反重力肌肉的肌肉激活,有和没有帕金森氏症。
    方法:十六(16)名参与者(9名帕金森氏症患者),年龄≥65岁。,在力平台(压力测量中心)上进行了4次平衡任务(双足和半串联睁眼和闭眼)的2×30-s试验;而在L5,股二头肌和腓肠肌上获得了双侧表面肌电图测量。肌电图振幅分析通过均方根(250ms窗口期)进行处理,并通过平衡任务期间的激活峰值进行归一化。来确定每个肌肉的活动水平。
    结果:帕金森氏症组报告说,在不同任务中,肌肉激活低于对照组(多裂的平均值=8%,股二头肌=16%,腓肠肌=7%),虽然没有统计学意义。帕金森氏症报告的姿势控制明显比对照组差,主要为中心摇摆椭圆区域(p=0.016)的压力来自半串联等挑战平衡任务。
    结论:在帕金森组中证实姿势控制不佳,但与躯干和下肢肌肉激活的变化无关,在平衡性能期间。
    BACKGROUND: Poor postural control has been reported in people with Parkinson\'s disease, which could be explained by the changes in muscular activation patterns related to antigravitational muscles. This study aims to measure the muscle activation of antigravitational muscles during balance tasks in individuals, with and without Parkinson\'s.
    METHODS: Sixteen (16) participants (9 with Parkinson\'s), aged ≥65 yrs., performed 2 × 30-s trials of 4 balance tasks (bipodal and semi-tandem opened eyes and closed eyes) on a force platform (center of pressure measurement); while surface electromyography measurements were obtained bilaterally on the multifidus at L5, biceps femoris and medialis gastrocnemius. Electromyography amplitude analysis was processed by the Root Mean Square (250 ms window epochs) and normalized by the peak of activation during the balance task, to determine each muscle\'s activity level.
    RESULTS: The Parkinson\'s group reported lower muscle activation than control across tasks (in mean for multifidus = 8%, biceps femoris = 16%, gastrocnemius = 7%), although not statistically significant. Parkinson\'s reported significantly poorer postural control than control, mainly for the center of pressure sway ellipse area (p = 0.016) from challenge balance tasks such as semi-tandem.
    CONCLUSIONS: Poor postural control was confirmed in the Parkinson\'s group, but not significantly associated by the changes from muscle activation of trunk and lower limbs, during balance performance.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    患有迟发性庞贝氏病(aLOPD)的成年人的特征是肌肉收缩组织恶化。然而,他们的神经肌肉表现鲜为人知。我们的目的是比较最大肌肉力量,激活,aLOPD和对照组之间的爆发力和神经肌肉疲劳。我们研究了20个aLOPD和20个匹配的对照。获得了髋部的等距最大自主收缩(MVC)扭矩,膝盖和脚踝肌肉。使用插值抽搐技术评估膝关节伸肌MVC期间的自愿激活水平(VAL)。通过快速收缩期间的扭矩发展速率(RTD)评估膝盖和脚踝肌肉的爆炸强度。在膝关节屈肌和伸肌收缩30秒期间测量神经肌肉疲劳。aLOPD中所有肌肉MVC扭矩均显著低于对照组(p<0.05)。最弱的肌肉是髋关节伸肌,其次是髋关节绑架者和绑架者。大多数肌肉的aLOPD中RTD的原始值较低(p<0.05)。没有报告标准化RTD的组间差异,VAL和神经肌肉疲劳(p值>0.05)。我们的研究表明,最大强度是具有近端-远端强度梯度的aLOPD中唯一受影响的神经肌肉特征。这表明aLOPD的存活肌肉组织在功能上与对照个体一样有效。
    Adults with late-onset Pompe disease (aLOPD) are characterized by muscular contractile tissue deterioration. However, their neuromuscular performances are poorly known. We aimed to compare maximal muscle strength, activation, explosive strength and neuromuscular fatigue between aLOPD and controls. We studied 20 aLOPD and 20 matched controls. Isometric maximum voluntary contraction (MVC) torque was obtained for the hip, knee and ankle muscles. The voluntary activation level (VAL) during knee extensor MVC was assessed using interpolated twitch technique. Explosive strength was evaluated for knee and ankle muscles through the rate of torque development (RTD) during fast contractions. Neuromuscular fatigue was measured during a 30-second contraction of knee flexors and extensors. All muscle MVC torques were significantly lower in aLOPD than controls (p <0.05). The weakest muscles were the hip extensors followed by hip abductors and abductors. Raw value of RTD was lower in aLOPD for the majority of muscles (p <0.05). No intergroup differences were reported for normalized RTD, VAL and neuromuscular fatigue (p-values> 0.05). Our study shows that maximal strength was the only neuromuscular characteristic affected in aLOPD with a proximal-distal intensity gradient. This suggests that the surviving muscle tissue of aLOPD is as functionally efficient as that of control individuals.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    暂无摘要。
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Sci-hub)

公众号