在爆发性自主收缩过程中,力量发展速度与皮质脊髓兴奋性相关。

Federico Castelli, Omar S Mian, Adam Bruton, Ashika Chembila Valappil, Ricci Hannah, Neale Anthony Tillin
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引用次数: 0

摘要

研究目的研究在爆发性自主收缩过程中扭矩发展速度(RTD)与皮质脊髓兴奋性(用运动诱发电位表示,MEP)之间的关系。同时,评估爆发性自主收缩不同阶段和最大自主收缩(MVC)高原时 MEP 和沉默期持续时间的差异。研究方法在 14 名成人中,分别在膝关节伸肌等长爆发性收缩时从 EMG 开始的约 45 毫秒(早期)、约 115 毫秒(中期)和约 190 毫秒(晚期)处测量股四头肌 MEP 和静默期持续时间,并在最大自主收缩高原时使用叠加经颅磁刺激(TMS)。在相同的收缩过程中,紧接着早期阶段 MEP 之前测量 RTD,并通过重复测量相关性 (RmCorr) 将这两个变量在参与者内部的不同收缩过程中相关联。在没有 TMS 的情况下,还测量了爆发性收缩早期、中期和晚期阶段的 RTD,并通过皮尔逊 r 相关性将其与相应阶段和之前阶段的 MEP 平均值相关联,以评估不同参与者之间的关系。在不同阶段和 MVC 高原时,对 MEP 和静默期持续时间进行比较(方差分析)。结果MEP 和 RTD 在参与者内部的不同收缩期之间存在相关性(RmCorr r=0.43),在中间阶段则在不同参与者之间存在相关性(Pearson's r=0.56)。MEP 和 RTD 在其他阶段没有相关性(r≥0.09)。静默期持续时间在收缩的不同阶段和 MVC 高原期都有所增加(方差分析,p= 0.001),但 MEP 保持不变(方差分析,p= 0.42)。结论MEP 和 RTD 之间的相关性表明皮质脊髓兴奋性是 RTD 的重要决定因素。在力矩快速发展期间以及直至 MVC 高原,皮质脊髓抑制增加,但兴奋性保持不变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rate of force development is correlated with corticospinal excitability during explosive voluntary contractions.
Objective: To investigate the relationship between rate of torque development (RTD) and corticospinal excitability (denoted by motor-evoked potential; MEP) during explosive voluntary contractions. Also, to assess differences in MEP and silent period duration between different phases of explosive contraction and at maximum voluntary contraction (MVC) plateau. Methods: In 14 adults, quadriceps muscle MEP and silent period duration were measured at ~45 (early), ~115 (middle), and ~190 ms (late) from EMG onset during knee-extensor isometric explosive contractions, and at MVC plateau with superimposed transcranial magnetic stimulation (TMS). RTD was measured immediately prior to early-phase MEP during the same contractions, and these two variables were correlated across separate contractions, within participants, via repeated measures correlation (RmCorr). RTD was also measured in explosive contractions without TMS over early-, middle-, and late-phases and correlated to MEP averaged across the corresponding and preceding phases, via Pearson's r correlations, assessing relationships across participants. MEP and silent period duration were compared (ANOVA) between the different phases and at MVC plateau. Results: MEP and RTD were correlated across separate contractions within participants (RmCorr r=0.43), and in the middle phase across participants (Pearson's r=0.56). MEP and RTD were not correlated in other phases (r≥0.09). Silent period duration increased throughout the different phases of contraction and up to MVC plateau (ANOVA, p= 0.001) but MEP remained constant (ANOVA, p= 0.42). Conclusion: The correlations between MEP and RTD suggests corticospinal excitability is an important determinant of RTD. During rapid torque development and up to MVC plateau, corticospinal inhibition increases but excitability remains constant.
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