[On the relations between the change in masticatory muscle thickness, performance force and index of firmness].
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In the present study, we investigated the structure and nerve innervation of the masseter, temporalis and zygomaticomandibularis of Suncus murinus which has no zygomatic arch. Detailed dissection of eight head halves of four S. murinus was performed. In S. murinus, small muscle bundle was observed to be adjoined with the lateral surface of the temporalis. This muscle bundle was completely separated from the masseter. Based on the positional relationships between the muscle bundle and supplying nerves, we conducted that the bundle corresponded to the zygomaticomandibularis of human described in our previous study (Shimokawa et al., 1999). In addition, some differences in the nerve distribution to the masticatory muscles were observed in S. murinus as compared with humans with respect to the following points: 1) The additional supplying branch to the masseter originated from the auriculo-temporal nerve: 2) The common trunk of the masseteric nerve and the nerve to the posterior part of the temporalis penetrated the superior head of the lateral pterygoid. A possible model to account for these differences based on the positional relationships among the muscles and supplying nerves is presented.
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Our work on a finite element model of the skull of Macaca aims to investigate the functional significance of specific features of primate skulls and to determine to which of the input variables (elastic properties, muscle forces) the model behavior is most sensitive. Estimates of muscle forces acting on the model are derived from estimates of physiological cross-sectional areas (PCSAs) of the jaw muscles scaled by relative electromyographic (EMG) amplitudes recorded in vivo. In this study, the behavior of the model was measured under different assumptions regarding the PCSAs of the jaw muscles and the latency between EMG activity in those muscles and the resulting force production. Thirty-six different loading regimes were applied to the model using four different PCSA sets and nine different PCSA scaling parameters. The four PCSA sets were derived from three different macaque species and one genus average, and the scaling parameters were either EMGs from 10, 20, 30, 40, 50 and 60 msec prior to peak bite force, or simply 100%, 50%, or 25% of peak muscle force. Principal coordinates analysis was used to compare the deformations of the model produced by the 36 loading regimes. Strain data from selected sites on the model were also compared with in vivo bone strain data. The results revealed that when varying the external muscle forces within these boundaries, the majority of the variation in model behavior is attributable to variation in the overall magnitude rather than the relative amount of muscle force generated by each muscle. Once this magnitude-related variation in model deformation was accounted for, significant variation was attributable to differences in relative muscle recruitment between working and balancing sides. Strain orientations at selected sites showed little variation across loading experiments compared with variation documented in vivo. These data suggest that in order to create an accurate and valid finite element model of the behavior of the primate skull at a particular instant during feeding, it is important to include estimates of the relative recruitment levels of the masticatory muscles. However, a lot can be learned about patterns of skull deformation, in fossil species for example, by applying external forces proportional to the estimated relative PCSAs of the jaw adductors.
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The EMG signals from left and right masseter and anterior temporal muscles of 40 healthy subjects were sampled at rest position and through gradually increased clench level to maximum voluntary contraction (MVC) at intercuspal position. A visual sense feedback of masseter muscle potential value was used for the subject to control clench level. The relationship between mean power frequency (MPF) and potential of EMG was investigated by a curvilinear regression of the second order. It was found that the relationship was of the second order logarithmic curve with maximum value of MPF. With the raising of the potential levels of EMG, the MPF increased at the lower clench levels and decreased at higher clench levels. The results indicate that controlling an identical clench level is necessary for using MPF to describe the functional state of masticatory muscles in the clinical situation.
Histologic examination of muscle biopsies and functional examination comprising electromyography and force measurements in a 19-yr-old boy with muscular dystrophy showed different wasting patterns of mandibular elevator and depressor muscles. Pronounced histopathologic changes were present in the masseter muscle, whereas pathologic findings in the anterior digastric muscle were limited to increased number of cells in slightly enlarged interfiber connective tissue. The masticatory pattern was distorted, and strength of mandibular elevator muscles was less than one third of the norm, whereas depressor strength corresponded more to reference values. This difference of muscular wasting might be caused by protective enzymes in the digastric muscle and/or functionally induced damage of the masseter. As affection from muscular dystrophy may vary greatly between the masticatory muscles, structural and functional examination should be used routinely to clarify prognosis before initiation of treatment procedures.
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