Sternohyoideus Muscles Research Articles

Surgical description and outcome of ultrasound-guided minimally invasive parathyroidectomy in 50 dogs with primary hyperparathyroidism.

To describe the surgical technique and clinical outcome of minimally invasive parathyroidectomy for primary hyperparathyroidism (PHPT) in the dog. Fifty client-owned dogs with PHPT that underwent minimally invasive parathyroidectomy. Retrospective cohort study. An ultrasound-guided mini lateral approach was made via a plane established between the sternocephalicus muscle and sternohyoideus muscles to expose the thyroid gland and enlarged parathyroid gland. Abnormal parathyroid glands were removed en bloc via partial thyroidectomy. The technique for bilateral disease was similar, the skin incision was made on midline and moved laterally to develop the above-mentioned plane of dissection. Age, sex, breed, bodyweight, ultrasound findings, histopathological diagnosis, surgical time, preoperative clinical signs, and clinical outcome were extracted from the records for descriptive statistics. A total of 62 glands were surgically removed, including 17 hyperplastic glands (17/62, 27.4%), 34 adenomas (34/62, 54.8%), and two carcinomas (2/62, 3.2%). Hypercalcemia resolved shortly after surgery in 44 dogs (44/45, 97.8%). One dog had recurrent hypercalcemia (1/45, 2.2%), one dog had persistent hypercalcemia (1/45, 2.2%), two dogs had permanent hypocalcemia requiring life-long calcitriol supplementation (2/45, 4.4%), and one dog died from clinical hypocalcemia (1/45, 2.2%). Minimally invasive parathyroidectomy was associated with a low morbidity and led to favorable outcomes in 44/45 dogs in this series. The results of this study supports the use of minimally invasive parathyroidectomy to treat PHPT in dogs.

Bifunctional Role of the Sternohyoideus Muscle During Suction Feeding in Striped Surfperch, Embiotoca lateralis.

SynopsisIn ray-finned fishes, the sternohyoideus (SH) is among the largest muscles in the head region and, based on its size, can potentially contribute to the overall power required for suction feeding. However, the function of the SH varies interspecifically. In largemouth bass (Micropterus salmoides) and several clariid catfishes, the SH functions similarly to a stiff ligament. In these species, the SH remains isometric and transmitts power from the hypaxial musculature to the hyoid apparatus during suction feeding. Alternatively, the SH can shorten and contribute muscle power during suction feeding, a condition observed in the bluegill sunfish (Lepomis macrochirus) and one clariid catfish. An emerging hypothesis centers on SH muscle size as a predictor of function: in fishes with a large SH, the SH shortens during suction feeding, whereas in fish with a smaller SH, the muscle may remain isometric. Here, we studied striped surfperch (Embiotoca lateralis), a species in which the SH is relatively large at 8.8% of axial muscle mass compared with 4.0% for L. macrochirus and 1.7% for M. salmoides, to determine whether the SH shortens during suction feeding and is, therefore, bifunctional—both transmitting and generating power—or remains isometric and only transmits power. We measured skeletal kinematics of the neurocranium, urohyal, and cleithrum with Video Reconstruction of Moving Morphology, along with muscle strain and shortening velocity in the SH and epaxial muscles, using a new method of 3D external marker tracking. We found mean SH shortening during suction feeding strikes (n = 22 strikes from four individual E. lateralis) was 7.2 ± 0.55% (±SEM) of initial muscle length. Mean peak speed of shortening was 4.9 ± 0.65 lengths s−1, and maximum shortening speed occurred right around peak gape when peak power is generated in suction feeding. The cleithrum of E. lateralis retracts and depresses but the urohyal retracts and depresses even more, a strong indicator of a bifunctional SH capable of not only generating its own power but also transmitting hypaxial power to the hyoid. While power production in E. lateralis is still likely dominated by the axial musculature, since even the relatively large SH of E. lateralis is only 8.8% of axial muscle mass, the SH may contribute a meaningful amount of power given its continual shortening just prior to peak gape across all strikes. These results support the finding from other groups of fishes that a large SH muscle, relative to axial muscle mass, is likely to both generate and transmit power during suction feeding.

Anterior trunk muscle shows mix of axial and appendicular developmental patterns.

Skeletal muscle in the trunk derives from the somites, paired segments of paraxial mesoderm. Whereas axial musculature develops within the somite, appendicular muscle develops following migration of muscle precursors into lateral plate mesoderm. The development of muscles bridging axial and appendicular systems appears mixed. We examine development of three migratory muscle precursor-derived muscles in zebrafish: the sternohyoideus (SH), pectoral fin (PF), and posterior hypaxial (PHM) muscles. We show there is an anterior to posterior gradient to the developmental gene expression and maturation of these three muscles. SH muscle precursors exhibit a long delay between migration and differentiation, PF muscle precursors exhibit a moderate delay in differentiation, and PHM muscle precursors show virtually no delay between migration and differentiation. Using lineage tracing, we show that lateral plate contribution to the PHM muscle is minor, unlike its known extensive contribution to the PF muscle and absence in the ventral extension of axial musculature. We propose that PHM development is intermediate between a migratory muscle mode and an axial muscle mode of development, wherein the PHM differentiates after a very short migration of its precursors and becomes more anterior primarily by elongation of differentiated muscle fibers.

Loss of FHL1 induces an age-dependent skeletal muscle myopathy associated with myofibrillar and intermyofibrillar disorganization in mice

Recent human genetic studies have provided evidences that sporadic or inherited missense mutations in four-and-a-half LIM domain protein 1 (FHL1), resulting in alterations in FHL1 protein expression, are associated with rare congenital myopathies, including reducing body myopathy and Emery-Dreifuss muscular dystrophy. However, it remains to be clarified whether mutations in FHL1 cause skeletal muscle remodeling owing to gain- or loss of FHL1 function. In this study, we used FHL1-null mice lacking global FHL1 expression to evaluate loss-of-function effects on skeletal muscle homeostasis. Histological and functional analyses of soleus, tibialis anterior and sternohyoideus muscles demonstrated that FHL1-null mice develop an age-dependent myopathy associated with myofibrillar and intermyofibrillar (mitochondrial and sarcoplasmic reticulum) disorganization, impaired muscle oxidative capacity and increased autophagic activity. A longitudinal study established decreased survival rates in FHL1-null mice, associated with age-dependent impairment of muscle contractile function and a significantly lower exercise capacity. Analysis of primary myoblasts isolated from FHL1-null muscles demonstrated early muscle fiber differentiation and maturation defects, which could be rescued by re-expression of the FHL1A isoform, highlighting that FHL1A is necessary for proper muscle fiber differentiation and maturation in vitro. Overall, our data show that loss of FHL1 function leads to myopathy in vivo and suggest that loss of function of FHL1 may be one of the mechanisms underlying muscle dystrophy in patients with FHL1 mutations.

Jaw muscle fiber type distribution in Hawaiian gobioid stream fishes: histochemical correlations with feeding ecology and behavior

Differences in fiber type distribution in the axial muscles of Hawaiian gobioid stream fishes have previously been linked to differences in locomotor performance, behavior, and diet across species. Using ATPase assays, we examined fiber types of the jaw opening sternohyoideus muscle across five species, as well as fiber types of three jaw closing muscles (adductor mandibulae A1, A2, and A3). The jaw muscles of some species of Hawaiian stream gobies contained substantial red fiber components. Some jaw muscles always had greater proportions of white muscle fibers than other jaw muscles, independent of species. In addition, comparing across species, the dietary generalists ( Awaous guamensis and Stenogobius hawaiiensis) had a lower proportion of white muscle fibers in all jaw muscles than the dietary specialists ( Lentipes concolor, Sicyopterus stimpsoni, and Eleotris sandwicensis). Among Hawaiian stream gobies, generalist diets may favor a wider range of muscle performance, provided by a mix of white and red muscle fibers, than is typical of dietary specialists, which may have a higher proportion of fast-twitch white fibers in jaw muscles to help meet the demands of rapid predatory strikes or feeding in fast-flowing habitats.

Organization of pERK-immunoreactive cells in trigeminal spinal nucleus caudalis, upper cervical cord, NTS and Pa5 following capsaicin injection into masticatory and swallowing-related muscles in rats

Many phosphorylated extracellular signal-regulated kinase (pERK)-immunoreactive (IR) cells are expressed in the trigeminal spinal subnucleus caudalis (Vc), upper cervical spinal cord (C1–C2), nucleus tractus solitarii (NTS) and paratrigeminal nucleus (Pa5) after capsaicin injection into the whisker pad (WP), masseter muscle (MM), digastric muscle (DM) or sternohyoideus muscle (SM). The pERK-IR cells also showed NeuN immunoreactivity, indicating that ERK phosphorylation occurs in neurons. The pERK-IR cells were significantly reduced after intrathecal injection of MEK 1/2 inhibitor PD98059. The pERK-IR cells expressed bilaterally in the Vc and C1–C2 after capsaicin injection into the unilateral DM or SM, whereas unilaterally in the Vc and C1–C2 after unilateral WP or MM injection. After capsaicin injection into the WP or MM, the pERK-IR cell expression in the Vc was restricted rostrocaudally within a narrow area. However, the distribution of pERK-IR cells was more wide spread without a clear peak in the Vc and C1–C2 after capsaicin injection into the DM or SM. In the NTS, the unimodal pERK-IR cell expression peaked at 0–720 μm rostral from the obex following capsaicin injection into WP, MM, DM or SM. In the ipsilateral Pa5, many pERK-IR cells were observed following capsaicin injection into the SM. The number of swallows elicited by distilled water administration was significantly smaller after capsaicin injection into the WP, MM or DM but not SM compared to that of vehicle-injected rats. Various noxious inputs due to the masticatory or swallowing-related muscle inflammation may be differentially involved in muscle pain and swallowing reflex activity.

Anomaly of the Sternothyroideus Muscle Insertion in a Dog

In this work, we describe an anatomic anomaly of the sternothyroideus muscle for the first time. The dissection of the left side of the neck of a young adult female dog showed a group of fibres of the sternothyroideus muscle diverging cranially and ventrally from the caudal region of the muscle onwards to be inserted at the thyrohyoideum bone, close to the insertion site of the sternohyoideus muscle. Dissection of the right aspect of the neck revealed a normal right sternothyroideus muscle. The consequence of the presence of this muscle strip was a link between the sternothyroideus muscle and the apparatus hyoideus, and it can be interpreted as a sign of the close phylogenetic relationship between the sternothyroideus and the sternohyoideus muscles.

Early osteological development of the fins in the hatchery-reared red porgy,Pagrus pagrus(L. 1758)

Summary The present study was undertaken to establish the normal, healthy features of morphological structures at various developmental stages as achieved under well-defined environmental culture conditions (temperature between 16 and 21°C, salinity 36 ppt, pH around 7.6, and oxygen saturation over 95%) common in aquaculture of the species. The pectoral fin supports began to develop at 2.90 mm total length (TL), followed by those of dorsal fins at 5.5 mm TL, caudal fins at 5.6 mm TL, pelvic fins at 5.9 mm TL and anal fins at 6.0 mm TL. The pelvic fins appeared fully at 7.4 mm TL. Development of dorsal lepidotrichia was first observed at 6.9 mm TL, attaining their final number at 7.6 mm TL. The dorsal spines first appeared at 6.5 mm TL and were complete at 7.4 mm TL. The anal lepidotrichia appeared during the development phase from 6.8 to 8.6 mm TL. At 5.6 mm TL, the upward flexion of the urostyle was initiated. The caudal lepidotrichia formed within the primordial fin at 5.6 mm TL and reached the final count at 7.4 mm TL. The caudal dermatotrichia first appeared at 7.3 mm TL and all forms were observed by 15.5 mm TL. The development pattern of fin supports found in Pagrus pagrus is quite similar to that described for other Sparid species.

Biting releases constraints on moray eel feeding kinematics

We present an analysis of prey capture functional morphology in eels by comparing two species of moray eels, Muraena retifera and Echidna nebulosa (Family Muraenidae), to the American eel Anguilla rostrata (Family Anguillidae). The skulls of both moray species exhibited extreme reductions of several prominent components of the suction-feeding mechanism, including the hyoid bar, the sternohyoideus muscle and the pectoral girdle. Associated with these anatomical modifications, morays showed no evidence of using suction during prey capture. From 59 video sequences of morays feeding on pieces of cut squid we saw no hyoid depression and no movement of prey toward the mouth aperture during the strike, a widely used indicator of suction-induced water flow. This was in contrast to A. rostrata, which exhibited a robust hyoid, sternohyoideus muscle and pectoral girdle, and used suction to draw prey into its mouth. Average prey capture time in morays, about 500 ms, was roughly 10 times longer than in A. rostrata, and morays frequently reversed the direction of jaw and head rotation in the midst of the strike. We tested whether the absence of suction feeding reduces temporal constraints on feeding kinematics, permitting greater variance in traits that characterize timing and the extent of motion in the neurocranium, by comparing moray eel species with A. rostrata, two Centrarchids and a cichlid. Kinematic variance was roughly 5 times higher in morays than the suction-feeding species. Prey capture by suction demands a rapid, highly coordinated series of cranial movements and the loss of this mechanism appears to have permitted slower, more variable prey capture kinematics in morays. The alternative prey capture strategy in morays, biting, may be tied to their success as predators in the confined spaces of reef crevices where they hunt for cephalopods, crustaceans and fish.

Interspecific variation in sternohyoideus muscle morphology in clariid catfishes: Functional implications for suction feeding

Depression of the hyoid apparatus plays a crucial role in generating suction, especially in fishes with a dorso-ventrally flattened head shape. It is generally assumed that shortening of the sternohyoideus muscle, which connects the hyoid to the pectoral girdle, contributes to hyoid depression. However, a recent study on the clariid catfish Clarias gariepinus has shown that this muscle does not shorten but elongates during this phase through retraction of the pectoral girdle. Here, we test whether this pattern is general among clariid catfish, or if variation in the morphology of the sternohyoideus may result in a different sternohyoideus behavior during hyoid depression. First, sternohyoideus mass, effective cross-sectional area, fiber length and fiber diameter were measured and compared for four clariid species. Next, velocity and magnitude of hyoid depression during prey capture (from high-speed videos), as well as patterns of sternohyoideus strain were analyzed (from high-speed X-ray videos) in these species. While morphology and hyoid depression performance varied considerably among these species, only the species with the most massive sternohyoideus, Gymnallabes typus, showed shortening of the sternohyoideus muscle during the initial part of the expansive phase. The data for Channallabes apus demonstrate that increasing the magnitude of hyoid depression does not necessarily require a shortening of the m. sternohyoideus, as it shows elongation of this muscle during hyoid depression.

In vitro estimates of power output by epaxial muscle during feeding in largemouth bass

Recent work has employed video and sonometric analysis combined with hydrodynamic modeling to estimate power output by the feeding musculature of largemouth bass in feeding trials. The result was an estimate of approximately 69 W kg(-1) of power by the epaxial muscle during maximal feeding strikes. The present study employed in vitro measurements of force, work and power output by fast-twitch epaxial muscle bundles stimulated under activation conditions measured in vivo to evaluate the power output results of the feeding experiments. Isolated muscle bundles from the epaxial muscle, the sternohyoideus and the lateral red or slow-twitch muscle were tied into a muscle mechanics apparatus, and contractile properties during tetanic contractions and maximum shortening velocity (Vmax) were determined. For the epaxial muscles, work and power output during feeding events was determined by employing mean stimulation conditions derived from a select set of maximal feeding trials: 17% muscle shortening at 3.6 muscle lengths/s, with activation occurring 5 ms before the onset of shortening. Epaxial and sternohyoideus muscle displayed similar contractile properties, and both were considerably faster (Vmax approximately 11-13 ML s(-1)) than red muscle (Vmax approximately 5 ML s(-1)). Epaxial muscle stimulated under in vivo activation conditions generated approximately 60 W kg(-1) with a 17% strain and approximately 86 W kg(-1) with a 12% strain. These values are close to those estimated by hydrodynamic modeling. The short lag time (5 ms) between muscle activation and muscle shortening is apparently a limiting parameter during feeding strikes, with maximum power found at an offset of 15-20 ms. Further, feeding strikes employing a faster shortening velocity generated significantly higher power output. Power production during feeding strikes appears to be limited by the need for fast onset of movement and the hydrodynamic resistance to buccal expansion.

Ontogeny of suction feeding capacity in snook,Centropomus undecimalis

The ontogeny of suction feeding performance, as measured by peak suction generating capacity, was studied in the common snook, Centropomus undecimalis. Suction pressure inside the buccal cavity is a function of the total expansive force exerted on the buccal cavity distributed across the projected area of the buccal cavity. Thus, the scaling exponent of peak suction pressure with fish standard length was predicted to be equal to the scaling exponent of sternohyoideus muscle cross-sectional area, found to be 1.991, minus the scaling exponent for the projected buccal cavity area, found to be 2.009, equal to -0.018. No scaling was found in peak suction pressure generated by 12 snook ranging from 94 to 314 mm SL, supporting the prediction from morphology. C. undecimalis are able to generate similar suction pressures throughout ontogeny.

A test of mouth-opening and hyoid-depression mechanisms during prey capture in a catfish using high-speed cineradiography

Detailed morphological analyses have identified a number of different mechanical pathways by which the morphologically complex cranial system of fishes can achieve mouth opening and hyoid depression. However, many of these proposed mechanisms remain untested. Furthermore, very little is known about the precise timing of activity of each of these mechanisms, and about the magnitude of each mechanism's total contribution to its proposed function. In the present study, all mouth opening and hyoid depression mechanisms described for Clarias gariepinus, an air-breathing catfish, are analysed. High-speed X-ray videos were recorded during prey capture of three catfish implanted with small, radio-opaque markers in the cranial elements potentially involved. A kinematic analysis was performed from which data were used as input in planar four-bar models. This analysis shows that the opercular mouth-opening mechanism initiates mouth opening, but is not able to cause the complete mouth openings as observed on the X-ray videos. The latter is accomplished through the protractor hyoidei muscles, which couple hyoid depression to lower jaw depression in a four-bar system and also reinforce lower jaw depression by shortening during the final stage of mouth opening. Although the angulo-ceratohyal ligament was previously hypothesised to play a part in mouth opening, our results show that it probably does not, but rather functions as a hyoid-elevator during mouth closure. Finally, hyoid depression is exclusively achieved by the four-bar mechanism involving neurocranial elevation and pectoral girdle retraction, generally without any reinforcement by shortening of the sternohyoideus muscle. In contrast to the results from a recent analysis on sunfish, the catfish's sternohyoideus gradually elongates during hyoid depression.

A functional morphospace for the skull of labrid fishes: patterns of diversity in a complex biomechanical system

The Labridae (including wrasses, the Odacidae and the Scaridae) is a species-rich group of perciform fishes whose members are prominent inhabitants of warm-temperate and tropical reefs worldwide. We analyse functionally relevant morphometrics for the feeding apparatus of 130 labrid species found on the Great Barrier Reef and use these data to explore the morphological and mechanical basis of trophic diversity found in this assemblage. Morphological measurements were made that characterize the functional and mechanical properties of the oral jaws that are used in prey capture and handling, the hyoid apparatus that is used in expanding the buccal cavity during suction feeding, and the pharyngeal jaw apparatus that is used in breaking through the defences of shelled prey, winnowing edible matter from sand and other debris, and pulverizing the algae, detritus and rock mixture eaten by scarids (parrotfishes). A Principal Components Analysis on the correlation matrix of a reduced set of ten variables revealed complete separation of scarids from wrasses on the basis of the former having a small mouth with limited jaw protrusion, high mechanical advantage in jaw closing, and a small sternohyoideus muscle and high kinematic transmission in the hyoid four-bar linkage. Some scarids also exhibit a novel four-bar linkage conformation in the oral jaw apparatus. Within wrasses a striking lack of strong associations was found among the mechanical elements of the feeding apparatus. These weak associations resulted in a highly diverse system in which functional properties occur in many different combinations and reflect variation in feeding ecology. Among putatively monophyletic groups of labrids, the cheilines showed the highest functional diversity and scarids were moderately diverse, in spite of their reputation for being trophically monomorphic and specialized. We hypothesize that the functional and ecological diversity of labrids is due in part to a history of decoupled evolution of major components of the feeding system (i.e. oral jaws, hyoid and pharyngeal jaw apparatus) as well as among the muscular and skeletal elements of each component.

Muscle fibre composition and electromyographic features of cervical muscles following prolonged head extension in growing rats.

Soft tissue stretching has been proposed as one of the control factors in craniofacial morphogenesis. However, its mechanism remains unclear. The present study investigated electromyographic (EMG) activity and muscle fibre composition of cervical muscles following prolonged head extension in growing rats. Thirty-six male Wistar rats were divided into two experimental (E1, E2) and one control (C) group at 25 days of age. To induce head extension, the experimental rats were raised in cylindrical cages, which were positioned horizontally for group E1 and tilted upward at 45 degrees for group E2. At 55 days of age, EMG activity was recorded from the anterior digastricus (AD), sternohyoideus (SH), sternomastoideus (SM), longus capitis (LC), and biventer cervicis (BC) muscles in the rest position and passive head extension. EMG activity was analysed on its integrated values (IEMG), and composition of muscle fibres was evaluated by myosin ATPase reaction and fibre cross-sectional areas were calculated. Group E1 showed a higher percentage of type I fibres and lower IEMG during passive head extension in AD. In group E2 there was a higher percentage of type I fibres, a higher IEMG at rest, and a lower IEMG during passive head extension in BC. The experimental groups demonstrated altered proportions of type IIA and IIB fibres in SM and LC. They also showed higher percentages of subtype fibres and reduced cross-section areas of type II fibres in most of the muscles investigated. These findings suggest that head extension affects fibre transition, distribution, cross-section area, and recruitment pattern in cervical muscles.

Tongue Bite Apparatus of Osteoglossomorph Fishes: Variation of a Character Complex

Osteoglossomorpha were first defined on the basis of two characters: (1) the parasphenoid-tongue bite apparatus (TBA); and (2) the presence of processes associated with the second hypobranchial and/or basibranchial element of the ventral gill arches. These two characters have continued to be cited as unambiguous support of the monophyly of this group of basal teleostean fishes. The TBA has been vaguely defined as a ‘‘bite’’ of gill arch dentition against that of the parasphenoid and palatoquadrate bones. Historical definitions include both plesiomorphic (e.g., enlarged teeth on palatoquadrate bones and gill arches) and apomorphic (e.g., enlarged teeth on the parasphenoid and a direct connection between the sternohyoideus muscle and the ventral gill arch skeleton) character states. Also, the processes associated with the second gill arches are likely components of the osteoglossomorph TBA by providing an additional attachment surface for the sternohyoideus (i.e., in addition to the sternohyoideus-urohyal connection). There is variation both of presence and form of these processes within osteoglossomorphs. To use both the presence or absence of a TBA as well as its component characters in systematic analyses artificially weights the value of this character complex. This character complex should not be used in place of, and especially not in addition to, its component characters.

Motor Patterns of Herbivorous Feeding: Electromyographic Analysis of Biting in the Parrotfishes Cetoscarus bicolor and Scarus iseri

The motor patterns of the herbivorous feeding bite were investigated in two species of parrotfish (Cetoscarus bicolor and Scarus iseri) with functionally distinct biting modes using electromyographic recordings. Behavioral data revealed that S. iseri utilized faster bites, took more bites per feeding bout, and bit at a higher frequency than did C. bicolor. EMGs recorded from the epaxialis (EP), levator operculi (LOP), 3 subdivisions of the adductor mandibulae (A1–A3), and the sternohyoideus (SH) muscles displayed a high degree of within-individual variance. Duration of muscle activity and onset time relative to LOP were shorter in S. iseri than in C. bicolor and S. iseri displayed a greater EMG amplitude in the LOP and SH muscles than did C. bicolor. We calculated the duty factors of the muscles as the relative timing of EMG variables divided by the total feeding cycle time. Patterns of duty factors of the feeding muscles were similar in both species, though muscles were active for a longer portion of the total bite cycle in S. iseri. In addition to its typical bite, S. iseri employed additional motor patterns when taking particularly hard bites. A multivariate comparison of EMGs from biting and suction feeding taxa revealed that the biting motor pattern was significantly different from suction feeding, although there was a high degree of overlap among all feeding strikes. The activity of the sternohyoideus muscle was significantly different between suction feeders and biters. Despite strong similarities of the general motor pattern in a wide range of teleost fishes, components of this pattern are shown to be evolutionarily plastic.

Scaling the feeding mechanism of the largemouth bass (Micropterus salmoides): motor pattern

We present the first analysis of scaling effects on the motor pattern of a feeding vertebrate. Data are presented for the effects of body size on the pattern of activity in four head muscles during prey capture in the largemouth bass, Micropterus salmoides. Electromyographic (EMG) recordings were made from three expansive-phase muscles (the epaxialis, the sternohyoideus and the levator arcus palatini) and one compressive-phase muscle (the adductor mandibulae), during the capture of small fish prey. Recordings were made of 181 prey-capture events from 19 bass that ranged in size from 83 to 289 mm standard length. We measured seven variables from the myogram of each capture to quantify the temporal pattern of muscle activation, including the duration of activity in each muscle and the onset time of each muscle, relative to the onset of the sternohyoideus muscle. Regressions of the mean value of each variable for the 19 individuals on standard length revealed that only the onset time of the adductor mandibulae changed with fish body size. The increase in onset time of the adductor muscle appears to reflect the longer time taken to open the mouth fully in larger fish. Other research shows that the kinematics of the strike in this species slows significantly with increasing body size. The combined results indicate that the duration of the EMG signal is not directly correlated with the duration of force production in muscles when compared between fish of different sizes. The lack of scaling of burst duration variables suggests that the reduced speeds of prey-capture motion are explained not by changes in the envelope of muscle activity, but rather by the effects of scale on muscle contractile kinetics. These scaling effects may include changes in the relative resistance of the jaw and head structures to movement through water and changes in the intrinsic contractile properties of the muscles of the feeding apparatus.

Effect of sternothyrohyoid myectomy on upper airway mechanics in normal horses.

The effect of transection of the sternothyroideus and sternohyoideus muscles on upper airway mechanics was investigated in exercising horses. Upper airway mechanics of six Standardbred horses were measured at rest and during exercise before and 24 h and 2 wk after sternothyrohyoid myectomy. Transnasal tracheal and pharyngeal catheters connected to differential pressure transducers were used to measure tracheal and pharyngeal pressures. A pneumotachograph mounted on the rostral end of an airtight face mask was used to measure airflow. Horses ran at 50, 75, and 100% of maximal O2 consumption on a treadmill. Twenty-four hours after sternothyrohyoid myectomy, no significant difference was detected in tracheal, pharyngeal, or translaryngeal inspiratory and expiratory pressures and impedances, inspiratory and expiratory flows, and respiratory frequency. Two weeks after sternothyrohyoid myectomy, there was a statistically significant increase in translaryngeal inspiratory pressure (P = 0.035) and tracheal inspiratory pressure (P = 0.032) compared with preoperative measurements. Two weeks after sternothyrohyoid myectomy, there was a statistically significant increase in translaryngeal inspiratory resistance (P = 0.017) and tracheal inspiratory resistance (P = 0.023) compared with preoperative values. Increased translaryngeal and tracheal inspiratory pressures and resistances after sternothyrohyoid myectomy suggest that the sternothyroideus and sternohyoideus muscles act to increase or maintain upper airway patency and stability in normal horses.

Ontogeny of feeding motor patterns in infant rats: an electromyographic analysis of suckling and chewing.

During mammalian ontogeny, there is a transition from suckling to the chewing of food. The question was asked: Is suckling a neuromuscular precursor to chewing, or are suckling and chewing independent systems? Electromyograms (EMGs) were recorded in rat pups of ages 6, 9, 12, 15, 18, and 21 days from the superficial masseter, anterior digastric, sternohyoideus, and genioglossus muscles during suckling and chewing. The EMG patterns of the 3 components of suckling behavior (nipple attachment, rhythmic sucking and the stretch response) are distinctive from one another and reflect the musculoskeletal biomechanics of suckling. Chewing EMGs are present by 12 days of age and attain the adult pattern by 18-21 days of age. During nipple attachment, pups exhibit a motor pattern that is similar to that of adult chewing, but other aspects of suckling differ from chewing in some EMG features. Comparison of EMGs between behaviors and between ages allowed interpretation of the degree of contunity of muscular activity across the suckling-to-chewing transition.