Hylander W L, Johnson K R
Duke University Medical Center, Department of Biological Anthropology and Anatomy, Durham, North Carolina 27710.
Am J Phys Anthropol. 1994 Aug;94(4):523-47. doi: 10.1002/ajpa.1330940407.
An analysis of in vivo bone strain indicates that the mandibular symphysis of macaques experiences lateral transverse bending or "wishboning" during the power stroke of mastication, and this loading regime results in relatively intense concentrations of stress along the lingual aspect of the symphysis (Hylander 1984, 1985). It has been hypothesized that peak wishboning of the macaque mandible, which probably occurs at the very end of the power stroke, that is, after the initial occurrence of maximum intercuspation, is associated with the late peak activity of the balancing-side deep masseter muscle coupled with the rapid decline in the activity of the balancing-side medial pterygoid and superficial masseter muscles (Hylander et al., 1987). The main purpose of this study is to do a detailed analysis of the electromyographic (EMG) activity of the deep and superficial masseter and medial pterygoid muscles so as to provide a better understanding of the external forces associated with wishboning. This was done by recording and analyzing EMG activity from the superficial masseter, deep masseter, and medial pterygoid muscles in macaques and baboons. EMG activity was recorded from bipolar fine-wire electrodes, and the data were quantified and analyzed using digital techniques. The EMG data clearly support our original observation that the balancing-side posterior deep masseter exhibits peak EMG activity relatively late in the power stroke at a time when activity is rapidly decreasing in the balancing-side medial pterygoid and superficial masseter muscles. Moreover, peak activity of the balancing-side deep masseter occurs at a time when the activity of the working-side deep and superficial masseter and medial pterygoid muscles are also decreasing. Thus, these data are consistent with the hypothesis that wishboning of the mandible is influenced significantly by the late occurrence of force from the balancing-side deep masseter. The EMG data also indicate that residual force from the relaxing superficial masseter may contribute significantly to wishboning. Finally, patterns of wishboning are not fully accounted for by our EMG analysis of the deep and superficial masseter and medial pterygoid muscles. This is probably because the lateral ptergyoids, which can either counter increased wishboning or actually cause reverse wishboning, were not included in our EMG analysis. The EMG data demonstrate that jaw-closing muscle recruitment patterns for macaques and baboons differ from those of humans. Nevertheless, in spite of these differences, it appears, based on previously published EMG data, that the human symphysis may also experience wishboning.(ABSTRACT TRUNCATED AT 400 WORDS)
一项对体内骨应变的分析表明,猕猴的下颌联合在咀嚼的动力冲程期间会经历横向弯曲或“叉骨状弯曲”,这种加载方式会导致联合舌侧出现相对强烈的应力集中(海兰德,1984年,1985年)。据推测,猕猴下颌骨的峰值叉骨状弯曲可能发生在动力冲程的末期,即在最大牙尖交错首次出现之后,这与平衡侧深层咬肌的晚期峰值活动以及平衡侧翼内肌和浅层咬肌活动的快速下降有关(海兰德等人,1987年)。本研究的主要目的是对深层和浅层咬肌以及翼内肌的肌电图(EMG)活动进行详细分析,以便更好地理解与叉骨状弯曲相关的外力。这是通过记录和分析猕猴和狒狒的浅层咬肌、深层咬肌和翼内肌的EMG活动来完成的。EMG活动通过双极细线电极进行记录,并使用数字技术对数据进行量化和分析。EMG数据清楚地支持了我们最初的观察结果,即平衡侧后部深层咬肌在动力冲程相对较晚的时候表现出EMG峰值活动,此时平衡侧翼内肌和浅层咬肌的活动正在迅速下降。此外,平衡侧深层咬肌的峰值活动发生在工作侧深层和浅层咬肌以及翼内肌的活动也在下降的时候。因此,这些数据与下颌骨叉骨状弯曲受平衡侧深层咬肌晚期发力显著影响的假设一致。EMG数据还表明,放松的浅层咬肌产生的残余力可能对叉骨状弯曲有显著贡献。最后,我们对深层和浅层咬肌以及翼内肌的EMG分析并未完全解释叉骨状弯曲的模式。这可能是因为在我们的EMG分析中没有包括翼外肌,翼外肌既可以对抗增加的叉骨状弯曲,也可以实际导致反向叉骨状弯曲。EMG数据表明,猕猴和狒狒的闭颌肌肉募集模式与人类不同。然而,尽管存在这些差异,但根据先前发表的EMG数据,人类的下颌联合似乎也可能经历叉骨状弯曲。(摘要截断于400字)