Variation of the mineral density in cortical bone may serve to keep strain amplitudes within a physiological range.

Within-bone variation in mineral density could be functional. A heterogeneous mineral-density distribution might serve to maintain habitual amplitudes of bone strain within a non-harmful, i.e., physiological range. Regions of a bone that would be strained the most on the basis of architecture alone might have a higher mineral density to make them more stiff and resistant to strain. We hypothesised that the cortical bone of the rabbit mandible contains such a functional distribution of mineral density. We thereby expected similar mineral-density patterns in the mandibles of different individuals due to the shared masticatory function. Secondly, we hypothesised that the highest mineral densities occur in mandibular regions predicted to be exposed to the largest amplitudes of strain-when taking into account bone architecture only. Mineral-density maps of the cortical bone of rabbit mandibles were obtained using micro-computed tomography (µCT). The µCT scans of two rabbits were converted into finite-element models (FEMs). To predict mandibular deformation during biting, these models were loaded by muscle forces and reaction forces. The forces acted on the condyles and on either the incisal or molar bite point. The FEMs were assigned a homogeneous material stiffness to calculate the strain amplitudes that would occur when only the architecture of the mandibular bone would be of influence. We found the cortical bone-mineral density patterns to be similar in all six mandibles. The mineral density of the corpus was higher than that of the ramus. A second consistent feature of the mandibular mineral-density distribution was that the medial ridge of the temporal-muscle insertion groove contained more mineral than its surrounding regions. The strain amplitudes calculated with the FEMs were variable and did not feature clear corpo-ramal differences. However, specific mandibular bone sites calculated to be exposed to the largest amplitudes of strain, including the medial ridge of the temporal-muscle insertion groove, did correspond with high-mineral-density regions. We conclude that, in the rabbit mandible, the heterogeneous mineral-density distribution might serve to suppress bone-strain amplitudes in regions architecturally susceptible to the largest deformations during loading.

Changes in rabbit jaw-muscle activity parameters in response to reduced masticatory load.

Mechanical food properties influence the neuromuscular activity of jaw-closing muscles during mastication. It is, however, unknown how the activity profiles of the jaw muscles are influenced by long-term alterations in masticatory load. In order to elucidate the effect of reduced masticatory load on the daily habitual activity profiles of three functionally different jaw muscles, the electromyograms of the masseter, temporalis and digastric muscles were recorded telemetrically in 16 male rabbits between seven and 20 weeks of age. Starting at eight weeks of age the experimental animals were fed significantly softer pellets than the control animals. Daily muscle activity was quantified by the relative duration of muscle use (duty time), burst number and burst length in relation to multiple activity levels. The daily duty time and burst number of the masseter muscle were significantly lower in the experimental group than in the control group at 5% and 10% of the maximum activity during the two weeks following the change in food hardness. By contrast, altered food hardness did not significantly influence the activity characteristics of the temporalis and digastric muscles. The findings suggest that a reduction in masticatory load decreases the neuromuscular activity of the jaw-closing muscles that are primarily responsible for force generation during mastication. This decrease is most pronounced in the weeks immediately following the change in food hardness and is limited to the activity levels that reflect muscle contractions during chewing. These findings support the conclusion that the masticatory system manifests few diet-specific long-term changes in the activity profiles of jaw muscles.

Is fiber-type composition related to daily jaw muscle activity during postnatal development?

AIM: Muscles containing large numbers of slow-contracting fibers are generally more active than muscles largely composed of fast fibers. This relationship between muscle activity and phenotype suggests that (1) changes in fiber-type composition during postnatal development are accompanied by changes in daily activity and (2) individual variations in fiber-type composition are related to similar variations in daily muscle activity. METHODS: The masseter and digastric muscles of 23 New Zealand White rabbits (young, juvenile and adult) were examined for their phenotype (myosin heavy chain content) and their daily activity (total daily number of activity bursts). RESULTS: During development, the masseter showed a strong increase in the number of fast-type fibers compared to the number of slow-type fibers. During development, also the number of powerful bursts in the masseter increased. The digastric showed no significant changes in fiber types or burst numbers. Within each muscle, across individual animals, no significant correlations (R < 0.70) were found between any of the fiber types and daily burst numbers in any of the age groups. CONCLUSIONS: The results suggest that activity-related influences are of relatively minor importance during development and that other factors are dominant in determining fiber-type composition.

Daily activity of the rabbit jaw muscles during early postnatal development.

Early postnatal development of the jaw muscles is characterized by the transition from suckling to chewing behavior. As chewing develops the jaw closing muscles become more powerful compared with the jaw openers. These changes are likely to affect the amount of daily muscle activity. Therefore, the purpose of this study was to characterize for a jaw opener (digastric) and jaw closer (masseter) the total duration of daily muscle activity (i.e. the duty time), and the daily burst numbers and lengths during early postnatal development. Using radiotelemetry the activity of these muscles was recorded in 10 young New Zealand White rabbits between three and eight weeks of age. Fiber-type composition was analyzed at eight weeks of age by determining the myosin heavy chain content of the fibers. During postnatal development both muscles showed no significant decrease or increase in their daily activity. However, the interindividual variation of the duty time and burst number significantly decreased. There were no significant differences between the digastric and masseter except for the most powerful activities at eight weeks of age, where the masseter showed a significantly higher duty time and burst number than the digastric. The masseter contained a higher number of slow-type fibers expressing myosin heavy chain-I and myosin heavy chain-cardiac alpha than the digastric. The present results suggest that the amount of jaw muscle activation is already established early during postnatal development, before the transition from suckling to chewing behavior. This amount of activation seems to be related to the number of slow-type fibers.

Fibre-type composition of rabbit jaw muscles is related to their daily activity.

Skeletal muscles contain a mixture of fibres with different contractile properties, such as maximum force, contraction velocity and fatigability. Muscles adapt to altered functional demands, for example, by changing their fibre-type composition. This fibre-type composition can be changed by the frequency, duration and presumably the intensity of activation. The aim of this study was to analyse the relationship between the spontaneous daily muscle activation and fibre-type composition in rabbit jaw muscles. Using radio-telemetry combined with electromyography, the daily activity of five jaw muscles was characterized in terms of the total duration of muscle activity (duty time) and the number of activity bursts. Fibre-type composition of the muscles was classified by analysing the myosin heavy chain content of the fibres. The amount of slow-type fibres was positively correlated to the duty time and the number of bursts only for activations exceeding 20-30% of the maximum activity per day. Furthermore, cross-sectional areas of the slow-type fibres were positively correlated to the duty time for activations exceeding 30% of the maximum activity. The present data indicate that the amount of activation above a threshold (> 30% peak activity) is important for determining the fibre-type composition and cross-sectional area of slow-type fibres of a muscle. Activation above this threshold occurred only around 2% of the time in the jaw muscles, suggesting that contractile properties of muscle fibres are maintained by a relatively small number of powerful contractions per day.

Burst characteristics of daily jaw muscle activity in juvenile rabbits.

Muscle activation varies with different behaviors and can be quantified by the level and duration of activity bursts. Jaw muscles undergo large anatomical changes during maturation, which are presumably associated with changes in daily muscle function. Our aim was to examine the daily burst number, burst length distribution and duty time (fraction of the day during which a muscle was active) of the jaw muscles of juvenile male rabbits (Oryctolagus cuniculus). A radio-telemetric device was implanted to record muscle activity continuously from the digastric, superficial and deep masseter, medial pterygoid and temporalis during maturation week 9-14. Daily burst characteristics and duty times were determined for activations, including both powerful and non-powerful motor behavior. All muscles showed constant burst numbers, mean burst lengths and duty times during the recording period. Including all behavior, the temporalis showed significantly larger daily burst numbers (205,000) and duty times (18.2%) than the superficial and deep masseter (90,000; 7.5%). Burst numbers and duty times were similar for the digastric (120,000; 11.1%) and medial pterygoid (115,000; 10.4%). The temporalis and deep masseter showed many short low activity bursts (0.05 s), the digastric showed many long bursts (0.09 s). For activations during powerful behaviors the superficial masseter and medial pterygoid had the largest burst numbers and duty times. Both muscles showed similar burst characteristics for all activation levels. It was concluded that activation of the jaw muscles is differently controlled during powerful and non-powerful motor behaviors and the functional organization of motor control patterns does not vary from 9 to 14 weeks of age.

Long-term registration of daily jaw muscle activity in juvenile rabbits.

Understanding control of muscles during various tasks and their adaptive changes requires information on all motor behavior used throughout the day. The total duration of muscle activity depends on the magnitude of its activation and can change during maturation. Therefore, the purpose of this study was to examine the duration of muscle activity (i.e. duty time) exceeding various activity levels in maturing jaw muscles. A telemetric device was implanted into nine juvenile male New Zealand White rabbits to continuously record muscle activity during maturation weeks 9-14. Electrodes were inserted into digastric, superficial and deep masseter, medial pterygoid, and temporalis muscles. Duty times (expressed as a percentage of time) were calculated for activation exceeding different levels (5-90%) of EMG peak activity per 24-h period. At 10 weeks of age, for activation exceeding the 5% level, the duty time of the temporalis (20.0+/-5.2%) was statistically significantly higher than that of the medial pterygoid (11.2+/-1.5%), digastric (11.0+/-5.1%), superficial (12.6+/-5.6%), and deep masseter (8.6+/-5.5%). Duty times declined with increasing activity level. For activation exceeding the 40% level the duty times of the superficial masseter and medial pterygoid were significantly higher than those of the other muscles. During maturation none of the muscles showed a significant change in duty time. However, for activation exceeding the 5% level, the inter-individual variation in duty time decreased significantly for the digastric, and superficial and deep masseter.

Variation in daily masticatory muscle activity in the rabbit.

The daily use of masticatory muscles remains largely unclear, since continuous recordings were limited in space and time. This study's purpose was to use radio-telemetry to examine daily muscle use and its inter- and intra-individual variations. A telemetric device was implanted into the rabbit masseter, and the transmitted signals were digitally stored for 7 days. Muscle use was analyzed by calculation of the total time each muscle was activated above 5, 20, and 50% of the day's peak activity. Rabbits (n = 6) spent only 2% of the time chewing. Muscles were activated up to 20% of the total time at levels exceeding 5% of peak activity, and only about 0.5% of the time in forceful behaviors utilizing 50% of maximum contraction. It can be concluded that daily muscle use remained constant during succeeding days, but differed significantly among muscle regions and individuals.

Passive force characteristics of an architecturally complex muscle.

In architecturally complex muscles with large attachment areas, it can be expected that during movement different muscle regions undergo different amounts of length excursions. As a consequence, the amount of passive force produced by the regions will differ. Therefore, we tested the hypothesis that during movement the vector of the passive force of such a muscle, which defines the magnitude, position and orientation of the resultant force of the various regions, has no fixed position, between the muscle's center of origin and insertion. As a model for an architecturally complex muscle we used the masseter muscle. It was expected that during jaw opening anterior muscle regions are more stretched than posterior regions, leading to an anterior shift of the passive force vector. A three-component force transducer was used to measure both the position and magnitude of passive force in the masseter muscle of 9 rabbits. Forces were recorded during repeated cycles of stepwise opening and closure of the jaw. The muscle exhibited a clear hysteresis: passive force measured during jaw opening was larger than that during jaw closing. With an increase of the jaw gape there was an approximately exponential increase of the magnitude of the passive muscle force, while simultaneously the passive force vector shifted anteriorly. Moment arm length of passive force increased by about 100%. This anterior shift contributed substantially to the increase of the passive muscle moment generated during jaw opening. It can be concluded that in architecturally complex muscles the increase of the passive resistance moment which is associated with muscle lengthening might not only be due to an increase of the magnitude of passive muscle force but also to an increase of the moment arm of this force.

A longitudinal electromyographic study of the postnatal maturation of mastication in the rabbit.

At 2 weeks of age, infant rabbits show chewing movements that resemble those of the adult animal. Previous studies have shown that, at that stage, the accompanying masticatory motor pattern is clearly similar to the suckling motor pattern. As early as 4 weeks, chewing muscle activity is indistinguishable from the adult chewing motor pattern. These reports suggest that the adult chewing motor pattern is developed from the suckling motor pattern. In this study, the chewing motor pattern in the intermediate period (between 2 and 4 weeks of age) was investigated by means of fine-wire electromyography and jaw tracking. Maturation of masticatory movements was found to have two phases. Maximum gape increased in the first few days and was followed by strong development of transverse jaw excursions after the age of 17 days. The increase in jaw excursions was brought about by changes in motor behaviour and facilitated by the development of smooth occlusal surfaces. The changes in motor behaviour were: (1) the level of activity of the balancing-side muscles became more equal to that of the working side; (2) the timing of digastric muscle activity became asymmetrical at the age of 17 days; (3) the peak activity of masseter, temporalis, medial pterygoid and lateral pterygoid muscle portions was gradually shifted or prolonged into the power-stroke phase. It can be concluded that the masticatory contraction pattern shifts from one derived from the suckling contraction pattern at the age of 14 days to one almost similar to the adult chewing pattern at the age of 23 days.

Differences in myosin heavy-chain composition between human jaw-closing muscles and supra- and infrahyoid muscles.

Jaw-closing muscles have architectural features suited to force production; supra- and infrahyoid muscles are better adapted to produce velocity and displacement. It was hypothesized that this difference in function would be reflected in myosin heavy-chain (MyHC) composition (equivalent to contraction velocity) and fibre-type cross-sectional area (equivalent to force). MyHC composition was determined in muscles obtained from eight human cadavers, using monoclonal antibodies against MyHC isoforms. Jaw closers contained 4.2 times fewer type IIA fibres and 5.2 times more hybrid fibres than suprahyoid muscles, and 3.9 times fewer type IIA fibres and 3.2 times more hybrid fibres than the infrahyoid muscles. In the jaw closers, MyHC-I was expressed in approx. 70% of all fibres (pure+hybrid), in the suprahyoid muscles in approx. 40%, and in the infrahyoid muscles in approx. 46%. In the jaw closers, type I fibres were 40% larger in diameter than in the supra- and infrahyoid muscles. It can be concluded that the jaw closers have characteristics of slow muscles, and that the supra-/infrahyoid muscles have characteristics of fast muscles.

Intermuscular and intramuscular differences in myosin heavy chain composition of the human masticatory muscles.

Among and within the human masticatory muscles a large number of anatomical differences exists indicating that different muscles and muscle portions are specialized for certain functions. In the present study we investigated whether such a specialization is also reflected by intermuscular and intramuscular differences in fibre type composition and fibre cross-sectional area. Fibre type compositions and fibre cross-sectional areas of masticatory muscles were determined in eight cadavers using monoclonal antibodies against myosin heavy chain (MyHC). The temporalis, masseter and pterygoid muscles could be characterized by a relatively large number of fibres containing more than one MyHC isoform (hybrid fibres). In these muscles a large number of fibres expressed MyHC-I, MyHC-fetal and MyHC-cardiac alpha. Furthermore, in these muscles type I fibres had larger cross-sectional areas than type II fibres. In contrast, the mylohyoid, geniohyoid and digastric muscle were characterized by less hybrid fibres, and by less fibres expressing MyHC-I, MyHC-fetal, and MyHC-cardiac alpha, and by more fibres expressing MyHC-IIA; the cross-sectional areas of type I and type II fibres in these muscles did not differ significantly. Compared to the masseter and pterygoid muscles, the temporalis had significantly larger fibres and a notably different fibre type composition. The mylohyoid, geniohyoid, and digastric muscles did not differ significantly in their MyHC composition and fibre cross-sectional areas. Also intramuscular differences in fibre type composition were present, i.e., a regionally higher proportion of MyHC type I fibres was found in the anterior temporalis, the deep masseter, and the anterior medial pterygoid muscle portions; furthermore, significant differences were found between the bellies of the digastric.

Architecture of the human jaw-closing and jaw-opening muscles.

BACKGROUND: The human jaw-closing and jaw-opening muscles produce forces leading to the development of three-dimensional bite and chewing forces and to three-dimensional movements of the jaw. The length of the sarcomeres is a major determinant for both force and velocity, and the maximal work, force, and shortening range each muscle is capable of producing are proportional to the architectural parameter volume, physiological cross-sectional area, and fiber length, respectively. In addition, the mechanical role the muscles play is strongly related to their three-dimensional position and orientation in the muscle-bone-joint system. The objective of this study was to compare relevant architectural characteristics for the jaw-closing and jaw-opening muscles and to provide a set of data that can be used in biomechanical modeling of the masticatory system. METHODS: In eight cadavers, sarcomere lengths, muscle masses, fiber lengths, pennation angles, and physiological cross-sectional areas were determined for the following muscles: superficial and deep masseter, anterior and posterior temporalis, anterior and posterior medial pterygoid, inferior and superior lateral pterygoid, posterior and anterior digastric, geniohyoid, posterior and anterior mylohyoid, and stylohyoid. To determine the spatial position of their action lines, the three-dimensional coordinates of the attachment sites were registered. RESULTS: Compared with the jaw openers, the jaw closers were characterized by shorter sarcomere lengths at the closed jaw, larger masses of contractile and tendinous tissue, larger physiological cross-sectional areas, larger pennation angles, shorter fiber lengths, shorter moment arms, and lower fiber-length-to-muscle-length ratios. In addition, architectural features differed across the muscles of the same functional group. Sarcomere length did not differ significantly among the regions of the same muscle. In contrast, in some muscles, significant intramuscular differences were found with respect to, e.g., physiological cross-sectional area, fiber length, pennation angle, and moment arm length. CONCLUSIONS: The results suggest that the jaw-closing muscles have architectural features that suit them for force production. Conversely, the jaw-opening muscles are better designed to produce velocity and displacement.

Three-dimensional structure of the human temporalis muscle.

BACKGROUND: The maximal force a muscle is capable of producing is proportional to its physiological cross-sectional area and its excursion range to the length of the muscle fibers. The length of the sarcomeres is a major determinant for both force and excursion range. The human temporalis muscle is an architecturally complex muscle, and little is known regarding the possible heterogeneous distribution of these parameters throughout the muscle. The objective of this study was to determine this distribution for different muscle portions and to examine the functional consequences. METHODS: In eight cadavers, sarcomere lengths, fiber lengths, and physiological cross-sectional areas were measured for the closed mouth position in six different anteroposterior portions of the temporalis muscle. To determine the spatial position of the muscle portions, the three-dimensional coordinates of attachment sites of a number of fiber bundles were registered. These parameters were used as input for a mathematical model with which sarcomere length changes and the consequences for the production of active force at different open positions of the jaw were estimated. RESULTS: At the closed-jaw position, average sarcomere length ranged between 2.26 and 2.34 microns and did not differ significantly among the muscle portions. Average fiber bundle length ranged between 21.7 and 28.9 mm and differed significantly among the muscle portions. The physiological cross-sectional area ranged between 1.82 and 2.93 cm2; the smallest values were found posteriorly, and the largest values anteriorly. The line of pull of the anteriormost muscle portion was slightly inclined anteriorly and medially, whereas the posteriormost portion was relatively strongly inclined backwardly and laterally. The model predicted that during jaw open-close movements a nonuniform change in length of the sarcomeres would occur; sarcomere excursions were smaller posteriorly than anteriorly. Different muscle portions seemed to function along different parts of the active length-force relationship. CONCLUSIONS: The temporalis muscle is an architecturally heterogeneous muscle. Different muscle portions are capable of producing different maximum force and excursion range, and the portions have the capability of performing different mechanical actions.

Architecture of the human pterygoid muscles.

Muscle force is proportional to the physiological cross-sectional area (PCSA), and muscle velocity and excursion are proportional to the fiber length. The length of the sarcomeres is a major determinant of both force and velocity. The goal of this study was to characterize the architecture of the human pterygoid muscles and to evaluate possible functional consequences for muscle force and muscle velocity. For the heads of the lateral and medial pterygoid, the length of sarcomeres and of fiber bundles, the PCSA, and the three-dimensional coordinates of origin and insertion points were determined. Measurements were taken from eight cadavers, and the data were used as input for a model predicting sarcomere length and active muscle force as a function of mandibular position. At the closed-jaw position, sarcomeres in the lateral pterygoid (inferior head, 2.83 +/- 0.1 microns; superior head, 2.72 +/- 0.11 microns) were significantly longer than those in the medial pterygoid (anterior head, 2.48 +/- 0.36 microns; posterior head, 2.54 +/- 0.38 microns). With these initial lengths, the jaw angle at which the muscles were capable of producing maximum active force was estimated to be between 5 degrees and 10 degrees. The lateral pterygoid was characterized by relatively long fibers (inferior, 23 +/- 2.7 mm; superior, 21.4 +/- 2.2 mm) and a small PCSA (inferior, 2.82 +/- 0.66 cm2; superior, 0.95 +/- 0.35 cm2), whereas the medial pterygoid had relatively short fibers (anterior, 13.5 +/- 1.9 mm; posterior, 12.4 +/- 1.5 mm) and a large PCSA (anterior, 2.47 +/- 0.57 cm2; posterior, 3.53 +/- 0.97 cm2).(ABSTRACT TRUNCATED AT 250 WORDS)

Amplitude and timing of EMG activity in the human masseter muscle during selected motor tasks.

Electromyographic (EMG) activity in the human masseter muscle was registered from six different sites, in the anterior, middle, and posterior regions of the superficial and deep layers of the muscle, during static clenching tasks (intercuspal and incisal), selected jaw movements (alternating protrusion/retrusion, right/left latero-deviation, and open/close excursions), and unilateral chewing on right and left sides. Peak-EMG amplitudes and the timing of the peaks were compared. Activity in the regions of the deep masseter was either higher (in mastication and intercuspal open/close excursions) or lower (incisal clenching) than the activities in the superficial masseter. Superficial and deep masseter also differed in their timing of peak EMG: During chewing, peak activity passed from superficial to deep in the balancing-side muscle, and from deep to superficial on the chewing side. During free latero-deviations, peak activity started in the deep masseter, when the jaw moved to the right side (i.e., the side of the muscle), and then passed to the superficial regions, after the jaw movement was reversed to the left side. In addition, within the deep masseter there existed clear anteroposterior differences in activation level (during incisal clenching and open/close excursions) and in timing (during latero-deviation). Such a differentiation of activity was not found in the superficial masseter.

Preweaning feeding mechanisms in the rabbit.

Muscle contraction patterns and mandibular movements of infant rabbits during suckling and chewing were compared. Oral muscle activity was recorded by fine-wire electromyography, while jaw movements and milk bottle pressure were registered. Suckling and mastication have a comparable cycle duration and share a common pattern of oral muscle activity which consists of a succession of a jaw closer burst, during which the jaw closes and undergoes a power stroke (in mastication), a suprahyoid burst with a stationary or slightly opening jaw and a digastric burst with fast jaw opening (the power stroke of suckling). Compared to suckling, mastication shows decreased jaw opener activity, increased jaw closer activity, development of jaw closing activity in the lateral pterygoid, and increased asymmetry in the masseter by development of a new differentiated motor pattern on the working side. The study shows that the suckling motor pattern enables the infant rabbits to change to chewing with just a few modifications.

Myosin heavy chain expression in rabbit masseter muscle during postnatal development.

The expression of isoforms of myosin heavy chain (MHC) during postnatal development was studied in the masseter muscle of the rabbit. Evidence is presented that in addition to adult fast and slow myosin, the rabbit masseter contains neonatal and 'cardiac' alpha-MHC. During postnatal growth myosin transitions take place from neonatal and fast (IIA, IIA/IIB--referring to a fibre containing both IIA and IIB MHCs) MHC to adult 'cardiac' alpha-MHC and I/alpha-MHC. Since there is a temporary population of fibres containing IIA/alpha-MHC during the first 4 wk of development with a peak in the 3rd to 4th wk, the transition from IIA-MHC to alpha-MHC may occur in these IIA/alpha-MHC-containing fibres. The appearance of 'cardiac' alpha-MHC coincides with the timing of weaning, suggesting that the changes in MHC content, that probably result in a transition to a lower speed of contraction, have functional significance related to weaning. The finding of neonatal MHC in adult rabbits indicates that the masseter develops at a rate and in a way that is distinct from most other skeletal muscles. A spatiotemporal variation in expression of myosin isozymes within the masseter was observed, with many fibres containing more than one myosin type, indicating developmentally regulated spatial differences in function.

Relationships between spindle density, muscle architecture and fibre type composition in different parts of the rabbit masseter.

The occurrence of muscle spindles was studied in the masseter muscle of rabbits by light-microscopy of whole muscle sections. The distribution of the spindles appeared to be heterogeneous. Most spindles lay in the anterior/deep and mid-parts of the masseter. The lateral/superficial part contained only a few muscle spindles. The distribution of the spindles is correlated to the distribution of slow twitch (type I) extrafusal fibres. This means that spindles, like type I fibres might be involved in the control of fine movements and posture. Spindle density and type I fibre density increase with distance from the temporomandibular joint. This could mean that spindles are involved in controlling bite force.

Histochemical and functional fibre typing of the rabbit masseter muscle.

The fibre-type distribution of the masseter muscle of the rabbit was studied by means of the myosin-ATPase and succinate dehydrogenase reactions. Six different fibre types were found and these were unequally distributed between and within the anatomical compartments of the muscle. Most of the masseter consists of slow- and fast-twitch oxidative fibres. The slow fibres increase in numbers in the deeper and more anterior regions of the muscle. Fast-twitch glycolytic fibres were almost exclusively found in the most posterior portions of the superficial and deep masseter. The fibre composition within the sagittally orientated anatomical compartments was found to be correlated with maximal contraction speeds during natural mastication as estimated from a mechanical model. However, the differences in fibre composition between the anatomical compartments (and hence between superficial and deep layers) appeared not to be correlated with contraction speed. The regional and compartmental specialisation within the masseter permits the muscle to perform many different functional roles in the generation and control of the jaw movements, jaw position and bite forces.