Masticatory muscles of the great‐gray kangaroo (Macropus giganteus)

The great‐gray kangaroo (Macropus giganteus) belongs to the Diprotodontia suborder (herbivorous marsupials of Australia) of the order of marsupials. We dissected the masticatory muscles in the great‐gray kangaroo and classified them based on their innervation. Three (two male and one female) adult great‐gray kangaroos (M. giganteus), fixed with 10% formalin, were examined. The masseter muscle of the great‐gray kangaroo was classified into four layers (superficial layers 1, 2, 3, and a deep layer), all innervated by masseteric nerves. Layer 1 of the masseter muscle was well developed and the deep layer inserted into the masseteric canal. The zygomaticomandibular muscle, which belongs to both the masseter and temporalis muscles, was innervated by both the masseteric nerve and posterior deep temporal nerve, and the temporalis muscle was innervated by the anterior and posterior deep temporal nerves. The medial pterygoid muscle, which was innervated by the medial pterygoid nerve, was divided into superficial and deep portions. The lateral pterygoid muscle was divided into superior and inferior heads by the buccal nerve. We propose that the relationship of the masticatory muscles in the kangaroo has evolved by passive anterior invasion of the deep layer of the masseter by the medial pterygoid muscle via the masseteric canal, associated with the development of an anteroposterior mode of mastication. Anat Rec 2007. © 2007 Wiley‐Liss, Inc.     

An anatomical study of the muscles innervated by the masseteric nerve

For an accurate assessment of jaw movement, it is critical to understand the comprehensive formation of the masseter. Detailed dissection was performed on fifteen head halves of eight Japanese cadavers in order to obtain precise anatomical information of the course and distribution of the masseteric nerve in the masseter, especially in the zygomaticomandibularis (ZM). Based on detailed innervation investigation, the main trunk of the masseteric nerve ran between ZM and the masseter, and the anterior region of ZM was closely related to the lateral layer of the masseter rather than the medial layer. Considering the positional relationships between the muscles and the innervating branches, it might be proposed that the muscle masses of ZM and the masseter migrate from the posterior side of the temporalis anterolateralward during development. This model is in agreement with the findings in that no nerve branch was observed between the temporalis and ZM.     

Masticatory Muscles and Branches of Mandibular Nerve: Positional Relationships Between Various Muscle Bundles and Their Innervating Branches

The masticatory muscles, which are composed of four main muscles, are innervated by branches of only one of the cranial nerves, the mandibular nerve. This muscle group has a variety of very complex functions. We have investigated the origins and insertions of the masticatory muscles and the adjacent bundles of the main muscles, and closely examined the positional relationships between the muscle bundles and innervating branches. According to the findings of the nerve branching patterns, the masticatory muscles can be classified into two groups: the inner group consisting of the lateral pterygoid muscle, and the outer group consisting of the other muscles and adjacent muscle bundles. Further, the outer muscle group is sub-divided into the three other main muscles (the masseter, the temporalis, and the medial pterygoid muscle) and the adjacent various transitional muscle bundles. Anat Rec, 302:609–619, 2019. © 2018 Wiley Periodicals, Inc.     

Lamination of the masticatory muscles in the kangaroo according to their innervation

An analysis of the laminations of the masseteric, zygomaticomandibular and temporalis muscles of the Red Kangaroo (Macropus Rufus) and all of the masticatory muscles of the Eastern Gray Kangaroo (Macropus Giganteus) was carried out based on their innervation. The masseteric muscle was divided into superficial and deep layers; the superficial layer was further subdivided into three laminae from the rostro-lateral portion to caudo-internal portion. The deep layer was divided into lateral, caudo-internal and rostro-internal laminae. The zygomaticomandibular muscle which was located between the masseteric and temporal muscles was divided into lateral, internal and rostral laminae, on the basis of its innervation. The lateral and internal laminae were innervated by the nerve which arises between the masseteric nerve and the posterior deep temporal nerve. A small rostral portion of the muscle was innervated by masseteric nerves, which passed through the internal lamina of the deep layer of the masseteric muscle. The temporalis muscle was innervated by an anterior deep temporal nerve and posterior deep temporal nerve. Only the most rostro-internal lamina of the temporalis muscle was innervated by the anterior deep temporal nerve. The anterior deep temporal nerve and lateral pterygoid nerve had a common trunk. We believe that the rostro-internal lamina was closely related to the lateral pterygoid muscle. The lateral pterygoid muscle displayed one lamina, whereas the medial pterygoid muscle was divided into internal and lateral laminae. The lateral lamina was further divided into rostro-internal and caudo-lateral laminae.     

Positional relationships between the masticatory muscles and their innervating nerves with special reference to the masseter and zygomaticomandibularis in Suncus murinus

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.     

Histochemical characteristics of the masseter and temporalis muscles of the rhesus monkey (Macaca mulatta)

The histochemical characteristics, cross-sectional area and capillary of the skeletal muscle fibers of the anterior and posterior regions of the superficial masseter and the temporalis muscles are described for juvnile and adult rhesus monkeys of both sexes. Slow twitch fatigue resistant (S), fast twitch fatigue resistant (FR) and fast twitch fatigable (FF) fibers were found in varying proportions throughout the muscles; however some fibers with an intermediate myofibrillar ATPase activity were observed in the anterior masseter. No significant differences for any of the variables were found between male and female juveniles for a specific muscle sample site. However, consideable variation was found between juvenile and adult and between adult male and female monkeys in the percentages of different fiber types and the cross-sectional area of fibers in specific regions of the superficial masseter and temporalis muscles. We conclude from these observations that significant differences in funtion exist both within and between the different masticatory muscles of rhesus monkeys. Functional differences may result from the pronounced sexual dimorphism evident in the dentofacial complex of rhesusmonkey.     

Positional relationships between the masticatory muscles and their innervating nerves with special reference to the lateral pterygoid and the midmedial and discotemporal muscle bundles of temporalis

For an accurate assessment of jaw movement, it is crucial to understand the comprehensive formation of the masticatory muscles with special reference to the relationship to the disc of the temporomandibular joint. Detailed dissection was performed on 26 head halves of 14 Japanese cadavers in order to obtain precise anatomical information of the positional relationships between the masticatory muscles and the branches of the mandibular nerve. After complete removal of the bony elements, the midmedial muscle bundle in all specimens and the discotemporal muscle bundle in 6 specimens, derivatives of the temporalis, which insert into the disc were observed. On the anterior area of the articular capsule and the disc of the temporomandibular joint, the upper head of the lateral pterygoid, the midmedial muscle bundle of temporalis and the discotemporal bundle of temporalis were attached mediolaterally, and in 3 specimens the posterosuperior margin of the zygomaticomandibularis was attached to the anterolateral area of the disc. It is suggested that these muscles and muscle bundles contribute to various mandibular movements. Although various patterns of the positional relationships between the muscles and muscle bundles and the their innervating nerves are observed in the present study, relative positional relationships of the muscles and muscle bundles and of nerves of the mandibular nerve are consistent. A possible scheme of the developmental formation of the masticatory muscles based on the findings of the positional relationships between the muscles and the nerves is presented.     

Functional morphology of the maxillo-mandibular apparatus in the miniature swine MINI-LEWE. 8. The development of the intramuscular nerve ramification pattern in the masticatory muscles

Postnatal changes in the intramuscular innervation pattern of the masticatory muscles of the miniature pig MINI-LEWE are only gradual. There are no definite relationships between the paths of nerves and the positions of the fasciae. The few anastomoses found were in the masseter muscle. The only other nerve found to be implicated in the motor innervation of the masticatory muscles was the motor root of the trigeminal nerve. Innervation studies are a good way of identifying the bounds of muscles: the masseter and zygomaticomandibularis muscles, for instance, are innervated jointly by the massetericus nerve, so that the zygomaticomandibularis muscle can be regarded as belonging to the masseter muscle.     

Histochemical characteristics of the masseter and temporalis muscles of the rhesus monkey (Macaca mulatta).

The histochemical characteristics, cross-sectional area and capillary of the skeletal muscle fibers of the anterior and posterior regions of the superficial masseter and the temporalis muscles are described for juvenile and adult rhesus monkeys of both sexes. Slow twitch fatigue resistant (S), fast twitch fatigue resistant (FR) and fast twitch fatigable (FF) fibers were found in varying proportions throughout the muscles; however some fibers with an intermediate myofibrillar ATPase activity were observed in the anterior masseter. No significant differences for any of the variables were found between male and female juveniles for a specific muscle sample site. However, considerable variation was found between juvenile and adult and between adult male and female monkeys in the percentages of different fiber types and the cross-sectional area of fibers in specific regions of the superficial masseter and temporalis muscles. We conclude from these observations that significant differences in function exist both within and between the different masticatory muscles of rhesus monkeys. Functional differences may result from the pronounced sexual dimorphism evident in the dentofacial complex of the rhesus monkey.     

Reducing condylar compression in clenching patients

The two major muscle groups used during clenching activity are the masseter and temporalis muscles. EMG readings of the masseter and temporalis muscles rise significantly during times of macro-clenching. Clenching occurs when the masseter and temporalis muscles contract, pulling the mandible superiorly. The continued contraction of the masseter and temporalis muscles results in compression forces on the teeth and temporomandibular joints. Theoretical joint loading models are utilized to demonstrate the load on the TMJ due to forces generated by the masseter and temporalis muscles. This study measures the EMG readings during bilateral macro-contraction of the masseter and anterior temporalis muscles. An appliance is fabricated to disengage the posterior teeth and a second series of EMG readings are taken to record lowered EMG readings. The vector forces of the reduced EMG's recordings demonstrate reduced condylar compression during macro-clenching.     

H-reflexes in masseter and temporalis muscles in man

In contrast with limb muscles, studies on H-reflexes in the trigeminal system are scarce. The present report aimed at reevaluating the responses obtained in the masseter and temporalis muscles after electrical stimulation of their nerves. Twenty-four subjects participated in the experiments. The reflexes were elicited in the masseter and temporal muscles by monopolar stimulation and recorded using surface electrodes. Stimulation of the masseteric nerve evoked an M-response in the masseter and an H-reflex in both the masseter and the temporal muscles. In contrast with the masseter muscle, where the homonymous H-reflex disappeared at higher stimulation intensities, the heteronymous temporal H-reflex remained and reached a plateau. Simultaneous stimulation of the masseteric and deep temporal nerves resulted in an M-response and an H-reflex in both the masseter and temporal muscles. Increasing stimulus intensitites led to disappearance of the H-reflex in both muscles. The results were compared with those obtained by others on limb muscles. As in these muscles, the presence of heteronymous H-reflexes in the jaw muscles can be used in future studies of motoneuronal excitability.     

The function of the disco-muscular apparatus in the human temporomandibular joint.

The morphology and function of the disco-muscular apparatus of the human TMJ is a controversial subject. Connections between the muscles which move the mandible and the "disco-capsular complex" have been described in a contradictory way. The disco-muscular apparatus is also described as being more extensive than that of the M. pterygoideus alone to include to the Mm. temporalis and masseter. However, the involvement of the latter is considered to be a peripheral variation of the normal anatomy and of little, if any, functional significance. The existence of independent relationships between the deep portions of the masseter and temporal muscles and the disco-capsular apparatus of the human TMJ is rarely discussed or explained. The morphologic findings were derived from fixed and unfixed human temporomandibular joints (TMJ) of varying ages and both sexes, whereby the functional maturity of the masticatory apparatus was taken into consideration. The results of the study show that aside from fibers originating from the superior venter of the M. pterygoideus lateralis, additional muscle or connective tissue fibers from the perimysium of the M. masseter are inserted to varying extents into the disc. The same is true for the M. temporalis, which is also directly connected to the disc via muscular or fibrous elements, or indirectly via fibers from the M. masseter. The insertion of the M. pterygoideus lateralis is always in the medial portion of the Discus articularis and those of the Mm. temporalis and masseter in the middle and lateral portions of the disc respectively. It is highly probable that a direct force transfer through the Mm. temporalis and masseter to the articular disc takes place, and that these muscles contribute to the movement of the disc during jaw movement, whereas the size and form of the muscle insertions are subject to a great deal of individual variation.     

The morphology of the mouse masticatory musculature

The mouse has been the dominant model organism in studies on the development, genetics and evolution of the mammalian skull and associated soft-tissue for decades. There is the potential to take advantage of this well studied model and the range of mutant, knockin and knockout organisms with diverse craniofacial phenotypes to investigate the functional significance of variation and the role of mechanical forces on the development of the integrated craniofacial skeleton and musculature by using computational mechanical modelling methods (e.g. finite element and multibody dynamic modelling). Currently, there are no detailed published data of the mouse masticatory musculature available. Here, using a combination of micro-dissection and non-invasive segmentation of iodine-enhanced micro-computed tomography, we document the anatomy, architecture and proportions of the mouse masticatory muscles. We report on the superficial masseter (muscle, tendon and pars reflecta), deep masseter, zygomaticomandibularis (anterior, posterior, infraorbital and tendinous parts), temporalis (lateral and medial parts), external and internal pterygoid muscles. Additionally, we report a lateral expansion of the attachment of the temporalis onto the zygomatic arch, which may play a role in stabilising this bone during downwards loading. The data presented in this paper now provide a detailed reference for phenotypic comparison in mouse models and allow the mouse to be used as a model organism in biomechanical and functional modelling and simulation studies of the craniofacial skeleton and particularly the masticatory system.     

Intramuscular nerve distribution pattern of the oblique and transverse heads of the adductor hallucis muscles in the human foot

To understand which layer of the intrinsic muscles of the foot the adductor hallucis muscle belongs to, it is essential to investigate the innervation patterns of this muscle. In the present study, we examined the innervation patterns of the adductor hallucis muscles in 17 feet of 15 Japanese cadavers. We investigated the intramuscular nerve supplies of the adductor hallucis muscles in six feet and performed nerve fiber analysis in three feet. The results indicate that: (i) the oblique head of the adductor hallucis muscle is divided into three compartments (i.e. lateral, dorsal and medial parts) or two compartments (i.e. dorsal and medial parts) based on its intramuscular nerve supplies, but we could not classify the transverse head into any parts; (ii) the communicating twig between the lateral and medial plantar nerves penetrated the oblique head of the adductor hallucis muscle in 13 of 17 feet (76.5%); (iii) the penetrating twig entered between the lateral and dorsal parts of the oblique head, passed between the lateral and medial parts of this muscle and then connected with the medial plantar nerve; and (iv) the majority of the nerve fibers of the penetrating twig derived from the lateral plantar nerve. The present study demonstrated that only the lateral part of the oblique head of the adductor hallucis muscle had a unique innervating pattern different from other parts of this muscle, suggesting that the lateral part of the oblique head has a different origin from other parts of this muscle.     

Innervation of human soft palate muscles

Our objective was to determine the branching and distribution of the motor nerves supplying the human soft palate muscles. Six adult specimens of the soft palate in continuity with the pharynx, larynx, and tongue were processed with Sihler's stain, a technique that can render large specimens transparent while counterstaining their nerves. The cranial nerves were identified and dissection followed their branches as they divided into smaller divisions toward their terminations in individual muscles. The results showed that both the glossopharyngeal (IX) and vagus (X) nerves have three distinct branches, superior, middle, and inferior. Only the middle branches of each nerve contributed to the pharyngeal plexus to which the facial nerve also contributed. The pharyngeal plexus was divided into two parts, a superior innervating the palatal and neighboring muscles and an inferior innervating pharyngeal constrictors. The superior branches of the IX and X nerves contributed innervation to the palatoglossus, whereas their middle branches innervated the palatopharyngeus. The palatoglossus and palatopharyngeus muscles appeared to be composed of at least two neuromuscular compartments. The lesser palatine nerve not only supplied the palatal mucosa and palatine glandular tissue but also innervated the musculus uvulae, palatopharyngeus, and levator veli palatine. The latter muscle also received its innervation from the superior branch of X nerve. The findings would be useful for better understanding the neural control of the soft palate and for developing novel neuromodulation therapies to treat certain upper airway disorders such as obstructive sleep apnea.     

Adaptation of the masseter and temporalis muscles following alteration in length, with or without surgical detachment

Histochemical properties, muscle fiber cross-sectional area, muscle fiber length, and the oxidative capacity of masticatory muscles of female rhesus monkeys were assessed following alteration in functional length by an intraoral appliance or by detachment of the muscle. Experimental groups received the appliance only (A); the appliance and subsequent detachment of the masseter (AD); the appliance and detached masseter, but with surgical reattachment of the masseter to the pterygomasseteric sling (ADR); no appliance, but detachment and reattachment of masseter (DR); or an appliance which was removed after 24 weeks to study posttreatment responses (PT). Animals were sacrificed and the muscles were studied at intervals from 4 to 48 weeks after initiation of the experimental period. The results of these studies led to the following conclusions: (1) Stretching the masseter and temporalis muscles within physiological limits did not significantly alter the proportion of fiber types, although oxidative capacity of the fibers was reduced. (2) Fibers with "intermediate" myofibrillar ATPase activity were no more prevalent in experimental than control muscles. (3) The cross-sectional area of Type I fibers of masseter muscles decreased following some experimental procedures, indicating that recruitment of these fibers is the most sensitive to altered jaw function. (4) Minimal alteration of muscle capillarity was induced by any of the experimental procedures. (5) The lengths of masseter muscle fibers in Group PT and of temporalis muscle fibers in groups AD and ADR were greater than in control animals.     

Innervation analysis of the small muscle bundles attached to the temporalis: truly new muscles or merely derivatives of the temporalis?

Detailed examinations were performed in ten temporal muscles from five cadavers to identify the muscle bundle arrangements of the temporalis and their innervation. Three additional muscle bundles were clearly observed in the main part of the fan-shaped temporalis: the anteromedial, anterolateral, and mid-lateral muscle bundles. Based on the origins, insertions and detailed innervation patterns, these bundles were considered as parts of the temporalis rather than independent muscles, although the anteromedial and anterolateral bundles had been recently reported as newly described muscles. A possible schematic model of the origins of these muscle bundles is proposed. We also report a branch from the posterior deep temporal nerve which was distributed to the temporal fascia and to the skin of the temporal region.     

Innervation analysis of the small muscle bundles attached to the temporalis: truly new muscles or merely derivatives of the temporalis?

Detailed examinations were performed in ten temporal muscles from five cadavers to identify the muscle bundle arrangements of the temporalis and their innervation. Three additional muscle bundles were clearly observed in the main part of the fan-shaped temporalis: the anteromedial, anterolateral, and mid-lateral muscle bundles. Based on the origins, insertions and detailed innervation patterns, these bundles were considered as parts of the temporalis rather than independent muscles, although the anteromedial and anterolateral bundles had been recently reported as newly described muscles. A possible schematic model of the origins of these muscle bundles is proposed. We also report a branch from the posterior deep temporal nerve which was distributed to the temporal fascia and to the skin of the temporal region.     

Location of the motoneurons innervating the transverse mandibular muscle in the guinea pig.

Motoneurons supplying the transverse mandibular muscle (TMM) in the guinea pig have been traced by injecting wheat germ agglutinin-horseradish peroxidase (WGA-HRP) in the TMM, and after applying HRP to the mylohyoid nerve. The TMM is bilaterally innervated by 22-36 motoneurons in each trigeminal motor nucleus, forming a column located ventrolaterally along the entire length of the superficial masseter motoneuron group. The axons are incorporated to the mylohyoid nerve. The location, the axon pathways in the brainstem and the pattern of the dentritic tree suggest that in the guinea pig the TMM motoneurons are involved in the masticatory movements in coordination with other jaw-closing muscles.