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Immunocytochemical analysis of the perinatal development of cat masseter muscle using anti-myosin antibodies.

The developmental changes in myosin gene expression in the masseter muscle of embryonic and juvenile kittens were examined immunocytochemically using anti-myosin heavy chain antibodies of various specificities. In the mature cat, this muscle contains only two phenotypes, the majority of fibres are superfast, the rest being slow fibres. In foetal tissues, the histological appearance of bundles of myotubes, comprising a large central myotube surrounded by a rosette of smaller myotubes, strongly suggest the existence in the jaw muscle of primary and secondary fibres during development. Immunocytochemical data are consistent with the hypothesis that there are four types of fibre; two types of primary fibre as well as two types of secondary fibre. (1) Slow primaries stain strongly with an anti-slow myosin antibody throughout the period under study. These fibres transiently express embryonic but not foetal myosin. (2) Superfast primaries stain for embryonic/foetal and slow myosins in the perinatal period but progressively replace these myosins with superfast myosin during postnatal development. (3) Superfast secondaries initially express embryonic/foetal myosins, but later, beginning around the time of birth progressively replace these myosins with superfast myosin. These fibres do not express slow myosin. (4) Slow secondaries, which initially also express embryonic/foetal myosins, but which postnatally express slow or slow and superfast myosins and express only slow myosin in the adult. These four types of fibres are homologous to the four isotypes of limb muscle fibres and may be derived from distinct lineages of myoblasts.

Animals↗

Characteristics of myofibres in the masseter muscle of mice during postnatal growth period.

Functional maturation of muscles is related to the constitutional proportion of muscle protein isoforms during development and growth. Although the mouse masseter muscle (MS) is classified as a fast limb muscle, its functions are different from those of a limb muscle. This study investigated the differentiation of myosin heavy chain (MHC) isoforms during the postnatal development periods in mouse MS and mouse tibialis anterior (TA), which is a fast limb muscle. Many anti-MHC slow-type-positive fibres were observed in neonatal MS and TA; these fibres decreased during development. Adult MS was composed of anti-MHC fast-type-positive fibres. MHC isoforms in MS were composed of MHC-2a and MHC-2d soon after birth. MHC-2b was expressed, but MHC-2a was not seen after 21 days. Expression of MHC-2b agreed with the weaning period, that is 2-3 weeks after birth. This fact suggested that the transformation from suckling to mastication changed the MHC isoforms during this period. In this study, the expressions of MHC-2b agree with the weaning period.

Aging↗

Patterns of masseter muscle activities during sleep in guinea pigs.

Basic neurophysiological mechanisms for sleep bruxism remain unknown. Analyses of masseter muscle activity during sleep in guinea pigs have shown that the duration and activity of masseter bursts differ between non-rapid eye movement (NREM) and rapid eye movement (REM) sleep and that some repetitive burst episodes do occur. Furthermore, masseter bursts occurred in association with a transient heart rate increase. These results suggest that various patterns of masseter bursts occur in association with transient arousal activity during sleep in guinea pigs.

Animals↗

Studies of biologic parameters for denture design. Part II: Comparison of masseter muscle activity, masticatory performance, and salivary secretion rates between denture and natural dentition groups.

Bilateral masseter muscle activities exerted during masticatory and salivary secretion rate tests of a group of 18 denture wearers were compared with a group of eight persons with 26 or more natural teeth. Denture wearers applied 22% to 39% of the muscle force applied by the ND group to chew peanuts or carrots and showed markedly lower masticatory performances. The average muscle activity was higher for chewing peanuts than carrots in the ND group but was similar for both test foods in the AD group. Motor discrimination seems to be intact in denture wearers, but their inability to tolerate high masticatory pressures may prevent them from exerting discriminatory forces comparable to those applied by persons with natural dentition when chewing relatively tough foods of varying hardness. The results indicate that the reduced muscle force applied by denture wearers is another important factor that contributes to their diminished chewing ability. Even though the denture wearers were older and applied less muscle activity during chewing, they produced slightly higher rates of stimulated parotid saliva than the ND group. This supports our previous findings and further indicates that the mucosal stimulation of dentures compensates for decreased muscle activity and absence of periodontal receptor stimulation for producing saliva in healthy denture wearers.

Adult↗

[Benefits and limits of sonography of the masseter muscle].

A sonographic method for diagnosis, follow-up and quantification of normal and hypertrophied masseter muscles is presented. This technique lends itself to diagnosis of macroscopic structural alterations of the muscle as well as tumors in the vicinity. Functional or microscopic tissue changes like trigger points in myofacial pain-dysfunction syndrome cannot be detected sonographically.

Adult↗

EMG activity of orbicularis oris superior, orbicularis oris inferior, and masseter muscles of mild and moderate articulatory disordered children.

The peak amplitude of EMG activity was measured from the orbicularis oris superior, orbicularis oris inferior, and masseter muscles for 3 mild and 3 moderately articulatory disordered and 3 normal children. The three groups showed similar levels of average peak EMG activity and variance across the three muscles, suggesting that the disordered children were free to vary their patterns of activity for these muscles when repeating a series of syllable tokens.

Articulation Disorders↗

EMG activity with the jaw fixed of orbicularis oris superior, orbicularis oris inferior and masseter muscles of mild and moderate articulatory disordered children.

The peak amplitude of EMG activity was measured from the orbicularis oris superior, orbicularis oris inferior, and masseter muscles of 3 mild and 3 moderately articulatory disordered and 3 normal boys repeating a series of /p ae/ syllable trains with the jaw fixed. Analysis showed similar levels of peak EMG amplitude and variability of performance for all subjects across the three muscles. These data were interpreted to suggest that speech-motor equivalence for simple articulatory acts requiring compensation is functioning within normal limits for the disordered subjects studied here.

Articulation Disorders↗

[Ectopic parotid gland in the mandible and masseter muscle].

An unusual case of double salivary ectopy of parotid gland is described into the masseter muscle and the mandibular ramus in a 45 year-old patient. He first was seen for a slow course tumefaction of the cheek. Imaging demonstrated the intramasseteric localization of the tumefaction and revealed a bone defect in the upper medial part of the mandibular ramus. The intramasseteric salivary ectopy has been confirmed by histologic examination.

Choristoma↗

Masseter muscle performance. Significance of structure and metabolism. A morphological and experimental study.

The aim of this thesis was to characterize structural factors in masticatory systems relevant to functional evaluations and to elucidate the effect on energy metabolism of electrically induced jaw muscle fatigue. An omnivorous masticatory system (the domestic pig) was compared morphologically with a carnivorous (the dog). Porcine masseter muscles were evaluated by ATP-ase histochemistry as well as with NADH-dehydrogenase and PAS-staining. Contractional characteristics were obtained from the porcine and canine masseters by electrical stimulation. The 133Xenon clearance technique and a flexible oxygen electrode were employed. A bite-force transducer was used. The porcine craniomandibular joint (CMJ) lacked a pronounced mandibular fossa and had anteriorly orientated cylindrical condyles. The dog CMJ comprised a cylindrical condyle orientated at right angles to the satittal plane and medially inclined. The pronounced mandibular fossa and marked tubercle, together with a well-developed retro-articular process, surrounded the condyle. The masticatory muscles were the same in the two species, except for the pig's zygomatico-mandibular muscle. The ATP-ase technique failed to reveal type II:B-fibres in the porcine masseter after acid and alkaline preincubation and it was not possible to separate fibre types by glycogen-staining and NADH-dehydrogenase histochemistry. These findings diverged from the pig soleus histochemical profile (type II:B-fibres 60%). The quantitative evaluation revealed 75% type II:A-fibres in the porcine masseter. No statistically significant difference was found between the various fibre-type diameters in the porcine masseter. The mean fibre Type diameter was larger in the porcine masseter than in the soleus muscle. Type II-fibres were more frequently found on the edge of the fascicles. The bite force recordings showed that the porcine masseter was capable of long endurance performance, in contrast to the easily fatigued canine masseter. Significant reductions of intramuscular substrates and a considerable lactate accumulation were observed. The NADH/NAD-shuttle was oppositely directed in the two species. The blood-flow recordings revealed a marked blood-flow impairment during contraction, followed by a prominent post-exercise hyperaemia. The pO2 recordings were closely related in time as well as in mangnitude to the blood flow. It is thus concluded, based on morphological observations, that the porcine masticatory system bears resemblance to the human situation. In the canine masseter muscle, a relationship was found between metabolism and mechanical bite-force output. This correlation was not so evident in the porcine masseter. Induced jaw muscle hyperactivity may lead to a reduced energy and redox state and, as a late consequence, to fatigue.

Animals↗

Unilateral masseter muscle hypertrophy: a case report.

Masseteric hypertrophy is a benign increase in the size of the masseter muscle, secondary to muscle hypertrophy. It produces facial asymmetry and is important in the differential diagnosis of other entities. The aim of this article is to report a case of unilateral masseteric muscle hypertrophy. The characteristics and diagnostic features of such alterations and options for treatment will be presented.

Adolescent↗

Effects of diet consistency on the myosin heavy chain mRNAs of rat masseter muscle during postnatal development.

To study the effects of diet consistency on the fiber phenotypes of rat masseter (1-70 days of age), the mRNAs of myosin heavy chain isoforms (MHC embryonic, neonatal, I, IIa, IId/x and IIb) were measured in total RNA preparations from masseters of hard-diet group (HDG) and soft-diet group (SDG) by competitive reverse transcriptase-polymerase chain reaction (RT-PCR). With respect to the time course of the transition of each MHC mRNA expressed as a percentage relative to the maximum mean, the soft diet facilitated early (9 days after weaning) expression of IId/x and IIb isoforms, and also a decline in the expression of neonatal and IIa isoforms. The expression of neonatal, IIa and IId/x isoforms at 70 days of age was significantly (P<0.05, P<0.01, P<0.01, respectively) lower in SDG than in HDG, indicating a higher relative composition of the IIb isoform in the SDG. Embryonic MHC mRNA had disappeared by 14 days of age (i.e. before weaning at 19 days). No MHC I mRNA was observed in any masseter studied. These results suggest that in the rat a soft diet facilitates an even more MHC IIb-rich phenotype in the masseter muscle than a hard diet.

Animals↗

Effect of motor tasks on the cortical topography of the human masseter muscle.

Non-invasive magnetic stimulation of the brain was earlier used to reveal the corticomotor representation of the human masseter muscle but it is unclear how motor tasks affect this map. An experimental approach incorporating transcranial magnetic stimulation of verified locations on the scalp, surface electromyography, and controlled muscle facilitation was used to disclose the corticomotor output map of the masseter during three isometric tooth-contact tasks, viz., tooth clenching in the intercuspal position, biting on the left molar teeth, and biting on the incisors. Map area was significantly different for all tasks, and map height and volume were also different for biting on the incisor teeth (p<0.05). There was evidence of task-related modulation of corticobulbar activity that appeared to be mainly of corticomotoneuronal origin, although the role of differential, task-associated peripheral afferent input from orofacial receptors could not be discounted.

Adult↗

Assessing mechanical sensitivity of masseter muscle in lightly anesthetized rats: a model for craniofacial muscle hyperalgesia.

In this report, we present a simple and reliable way of assessing mechanical sensitivity of masseter muscle as a model for craniofacial muscle hyperalgesia. Mechanical thresholds that evoke nocifensive hindpaw responses following noxious masseter stimulation were assessed. Masseteric injections of widely used sensitizing agents significantly increased mechanical sensitivity of the muscle in a time dependent manner without affecting other muscles and overlying skin. This lightly anesthetized rodent paradigm allows us to provide calibrated and reliable mechanical stimulus, which is not possible in behaving animals. The technique can be applied to study mechanistic bases for craniofacial muscle tenderness.

Analgesics, Non-Narcotic↗

Length changes in the human masseter muscle after jaw movement.

The human masseter is a multilayered, complex muscle contributing to jaw motion. Because variations in stretch may cause muscle fibers to function over different portions of their length-tension curves, the aim of this study was to determine how parts of the masseter lengthen or shorten during voluntary jaw movements made by living subjects. Magnetic resonance (MR) imaging and optically-based jaw-tracking were used to measure muscle-insertion positions for four parts of the muscle with six degrees of freedom (DOF), before and after maximum-opening, jaw protrusion and laterotrusion in four adult males. Muscle part lengths and intramuscular tendon lengths were calculated, and these data, with fiber-tendon ratios published previously, were used to estimate putative changes in fiber-length. During maximum jaw-opening, the largest increases in muscle length (34-83%) occurred in the medial part of the deep masseter, whereas the smallest changes occurred in the posterior-most, superficial masseter (2-19%). Smaller changes were found during movement to the ipsilateral side, than during protrusion and movement to the contralateral side. On maximum opening, putative fibers in the deep masseter lengthened up to 83%, whereas those of the superficial masseter stretched up to 72%. The masseter muscle does not stretch uniformly for major jaw movement. Jaw motion to the ipsilateral side causes little length change in any part, and the effect of tendon-stretch on estimated fiber lengths is not substantial. The stretch that occurs infers there are task-related changes in the active and passive tensions produced by different muscle regions.

Adult↗

Reflex responses of motor units in human masseter muscle to electrical stimulation of the lip.

The reflex responses of single motor units in human masseter muscle to electrical stimulation of the lip were recorded. The subject maintained a content mean level of pre-stimulus excitation of the parent motor neurone by biting in such a way that the unit fired at either 10 or 15 Hz during each trial. When firing at 10 Hz, most units were reflexly inhibited for up to 90 ms by electrical stimuli at intensities that were perceived to be mildly uncomfortable. In many units, the inhibition consisted of 2 phases which were separated from each other by a few spikes occurring about 30 ms after the stimulus. It was occasionally possible to evoke only the latter phase (latency about 40 ms) with stimulus at intensities near the response threshold. In these instances, the inhibitory response became biphasic at higher stimulus intensities with the emergence of a shorter (10-15 ms) component. Still higher intensities caused the 2 phases of inhibition to merge, giving the appearance of a single, prolonged, inhibitory response. When the pre-stimulus firing frequency of the unit was changed from 10 Hz to 15 Hz, the inhibitory responses to the same stimuli were decreased, with the longer-latency component usually surviving beyond the shorter-latency phase. The pattern of reflex responses observed can be explained by a model based on information derived from intracellular recordings in animal experiments.

Action Potentials↗

Vestibular and somatosensory afferents modulate masseter muscle activity.

The aim of the research was to investigate whether somatosensory impulses starting from the forelimbs could modulate masseter muscle activity in anesthetized guinea pigs. The effect of interactions between radial nerve and vestibular stimulations on the masseter motor unit responses was also studied. Results show that electrical stimulation of both radial nerves induces responses in the masseter motor units most frequently characterized by excitation at latency ranging from 14 to 29 ms. The radial nerve responses were strongly reduced by conditioning electrical stimulation of the vestibular ampullar receptors. Similarly, the vestibular responses were reduced by conditioning radial nerve stimulation. The natural activation of the vestibular macular receptors can either decrease or increase the masseter motor unit responses evoked by electrical stimulation of the radial nerve. These complex inhibitory-excitatory interactions between the two sensory inputs could control the masseter postural tone in relation to the head and limb positions in space.

Animals↗