Weijs W A, Korfage J A, Langenbach G J
Department of Anatomy and Embryology, Academic Centre for Dentistry Amsterdam (ACTA), The Netherlands.
J Anat. 1989 Feb;162:133-48.
In the rabbit, jaw opening and closing occurs in combination with condylar protrusion and retraction. Consequently the centre of rotation (CR) for the movement lies in the inferior portion of the ascending ramus of the mandible, far below the condyle. This location is stable and independent of the type of food being chewed and the age of the animal. The topography of the soft tissues at the posterior border of the ramus is adapted to the movement pattern. The facial nerve crosses the space between skull and mandible at the level of the CR. The parotid gland lies behind the ramus between condyle and CR; below the CR, the gland is replaced by loose adipose tissue. A computer model was used to demonstrate that the location of the CR determines the amount of stretch of the large masseter and medial pterygoid muscles. Using parameters for passive elastic behaviour of muscle, obtained by postmortem measurements, it can be shown that the normal CR position minimises muscle stretch and passive elastic forces. Even a small upward displacement of the CR causes a significant amount of resistance in the jaw-closers at gapes comparable to those reached in natural mastication. A second, less dramatic effect of increased muscle stretch is a sharper decline of maximum possible active closing force, due to the interrelationship of fibre length and isometric tension. In young animals, the muscle fibres are relatively long but stiff; in adults they are shorter, but more compliant. In both ages the CR is located in such a way that masseter and medial pterygoid stretching is minimised. The high position of the temporomandibular joint ensures a maximal leverage for the muscles mentioned above. By separating the point where the reaction forces apply (the joint) from the location of the rotational axis, maximum leverage and minimal length changes of the jaw-closing muscles are achieved simultaneously. It is further suggested that elastic muscular forces play a role in determining the position of the CR.
在兔子中,张口和闭口动作与髁突的前伸和后缩相结合。因此,该运动的旋转中心(CR)位于下颌升支的下部,远在髁突下方。这个位置是稳定的,与所咀嚼食物的类型和动物的年龄无关。下颌升支后缘的软组织形态适应这种运动模式。面神经在CR水平穿过颅骨和下颌骨之间的间隙。腮腺位于髁突和CR之间的下颌升支后方;在CR下方,腮腺被疏松的脂肪组织取代。使用计算机模型证明,CR的位置决定了咬肌和翼内肌的拉伸程度。利用死后测量获得的肌肉被动弹性行为参数,可以表明正常的CR位置可使肌肉拉伸和被动弹力最小化。即使CR有很小的向上位移,在与自然咀嚼时达到的张口度相当的情况下,也会在闭口肌中产生显著的阻力。肌肉拉伸增加的第二个不太显著的影响是,由于纤维长度和等长张力的相互关系,最大可能的主动闭口力会急剧下降。在幼年动物中,肌肉纤维相对较长但僵硬;在成年动物中,它们较短,但更具柔韧性。在这两个年龄段,CR的位置都能使咬肌和翼内肌的拉伸最小化。颞下颌关节的高位确保了上述肌肉的最大杠杆作用。通过将反作用力施加的点(关节)与旋转轴的位置分开,可同时实现闭口肌的最大杠杆作用和最小长度变化。进一步表明,弹性肌肉力在确定CR的位置中起作用。