Movements of the cranial vibrissae in the Golden hamster (Mesocricetus auratus)

Vibrissae are highly refined vibrotactile receptors that are present on most mammals. The Golden hamster exhibits three different behaviours of its mystacial, supraorbital, and genal vibrissae. During rest, all the vibrissae are reclined and motionless. When hamsters are alert, the vibrissae are partly or fully erect and essentially motionless. During active investigation, the mystacial vibrissae "whisk" or "sweep" through antero–posterior excursions. The genal vibrissa moves only slightly in periodic erection. The supraorbital vibrissae carry through a wide erection arc and have limited excursions with movements of the upper eyelid. The mystacial vibrissae whisk quickly (about 16 sweepsls). Whisking is divisible into contact (relatively high amplitude, low frequency), non–contact (relatively low amplitude, high frequency), and double–pump (combination contact and non–contact) types, and can be either bilaterally symmetric or asymmetric. The dimensions of the mystacial territory around the snout change throughout whisking due to coordinated changes in the shape of the mystacial pad and the tilting of the vibrissae relative to the pad. Such differential movements have implications for sensory physiology as they point to an ability for fine sensory monitoring of the environment.     

Phenoxyethanol as a nontoxic preservative in the dissection laboratory

In an effort to rid the dissection room of irritating and potentially health-threatening toxic chemicals, we have modified the phenoxyethanol technique for long-term preservation of embalmed cadavers. The new methods employ faster, less toxic embalming and reduced or eliminated phenoxyethanol immersions. Our results are comparable with or improved over those previously described and demonstrate that phenoxyethanol is an excellent, easily manageable alternative preservative to standard formaldehyde/phenol-based embalming fluids.     

Beta-agonist-induced alterations in organ weights and protein content: comparison of racemic clenbuterol and its enantiomers

Clenbuterol is a relatively selective beta2-adrenergic partial agonist that has bronchodilator activity. This drug has been investigated as a potential countermeasure to microgravity- or disuse-induced skeletal muscle atrophy because of presumed anabolic effects. The purpose of this study was to: 1) analyze the anabolic effect of clenbuterol's (-)-R and (+)-S enantiomers (0.2 mg/kg) on muscles (cardiac and skeletal) and other organs; and 2) compare responses of enantiomers to the racemate (0.4 mg/kg and 1.0 mg/kg). Male Sprague Dawley rats were treated with: a) racemic clenbuterol (rac-clenbuterol, 0.4 or 1.0 mg/kg); b) enantiomers [clenbuterol (-)-R or (+)-S]; or c) vehicle (1.0 mL/kg buffered saline). Anabolic activity was determined by measuring tissue mass and protein content. HPLC teicoplanin chiral stationary phase was used to directly resolve racemic clenbuterol to its individual enantiomers. In skeletal muscle, both enantiomers had equal anabolic activity, and the effects were muscle- and anatomic region-specific in magnitude. Although the enantiomers did not affect the ventricular mass to body weight ratio, clenbuterol (+)-S induced a small but significant increase in ventricular mass. Both clenbuterol enantiomers produced significant increases in skeletal muscle mass, while being less active in producing cardiac ventricular muscle hypertrophy than the racemic mixture.     

Development of the masseter muscle and oral behavior in the pig

During mastication the adult pig masseter contracts with a complex pattern involving a wave of electromyographic (EMG) activity moving from the ventro-rostral corner to the dorso-caudal corner. The present study was undertaken to ascertain the ontogeny of that contraction pattern. Anatomical measurements were made on masseters from fetal, infant, and juvenile pigs. EMG activity from different parts of the masseter was recorded along with oral movements in infant and juvenile pigs as they suckled, drank, and chewed on food and non-food objects. The basic arrangement of muscle fibers and tendinous aponeuroses was found to be the same in all ages. The longest and most vertical fibers were found rostrally and ventrally, whereas the shortest and most horizontal fibers were found caudally and dorsally. The length of fasciculi decreased with age, relative to muscle weight. Variance in length among different parts of the muscle increased with age. Fetal masseters were oriented generally more horizontally than the masseters of older animals, except that the dorso-caudal corner, usually the most horizontal portion, is not developed in fetuses. The contraction patterns within the infant masseter were less complex than those of older animals; only the dorso-caudal corner was distinct. The further development of intramuscular differences in activity may be associated with the increasing anatomical complexity of the masseter, which augments its functional capabilities.     

Facial morphology and vibrissal movement in the golden hamster

The major cranial vibrissae in the golden hamster can be moved in complex ways that suggest they are served by a finely controlled motor system. Movements are hypothesized to be the products of differential blood flow and pressure regulation in the sinus surrounding each vibrissal follicle, contractions of the striated facial muscles, and elastic rebound in the connective tissues. The vasculature contributes hydrostatic forces that erect the vibrissae slightly and distort their connective tissue bedding, rigidify the vibrissal capsules, thus forming firm bases of attachment for certain facial muscles, and theoretically provide a pressure plate around the follicle, important in lowering the firing thresholds of receptor endings. The facial muscles supply the major forces in erection and protraction of the vibrissae by acting on both the capsules and the connective tissue bedding. The connective tissues are organized into capsular and extracapsular systems that serve to stabilize the vibrissae and return them to initial rest positions. The slight movements of the genal vibrissa are the effects of vascular and connective tissue dynamics, the musculature being uninvolved. Wide angle movements of the supraorbital vibrissae are products of the vasculature and connective tissues, plus contractions of the Mm. orbicularis oculi and frontalis. Mystacial vibrissal movement is quite complex. The vasculature supplies a small degree of capsular erection and mystacial pad distortion, but primarily rigidifies the capsules. The bulk of erection and protraction is produced by the M. nasolabialis profundus (NLP) and the vibrissal capsular muscles (VCM). The NLP distorts the mystacial pad; the VCM tilt the capsules relative to the pad. Retraction is mainly accomplished by elastic rebound in the pad, this being aided in its extreme degrees by the Mm. nasolabialis and maxillolabialis. The Mm. nasolabialis superficialis and buccinator pars orbicularis oris help to spread the vibrissae into a dorsoventral fan and stabilize the mystacial pad during whisking.     

Changes in muscle proteins and spermidine content in response to unloading and clenbuterol treatment

Anabolic agents such clenbuterol (Cb) are useful tools for probing the mechanisms by which muscles respond to disuse. Cb was examined under different loading conditions with respect to its effects on muscle mass, protein (myofibrillar and cytosolic), and spermidine content in mature male rats. Compared with control treatment, Cb significantly increased loaded and unloaded soleus, plantaris, and extensor digitorum longus (EDL) mass. Likewise, Cb significantly increased loaded and unloaded soleus (24.8 and 21.6%, respectively), plantaris (12.1 and 22.9%, respectively), and EDL (22.4 and 13.3%, respectively) myofibrillar protein content. After unloading, cytosolic proteins significantly increased in the EDL but decreased in the soleus and plantaris. Cb significantly increased cytosolic protein levels in all loaded muscles, while only causing increases in unloaded soleus. When compared with controls, unloading caused significant reductions in spermidine levels in the soleus (40.4%) and plantaris (35.9%) but caused increases in the EDL (54.8%). In contrast, Cb increased spermidine levels in unloaded soleus (42.9%), plantaris (102.8%), and EDL (287%). In loaded muscles, Cb increased spermidine levels in all three muscles, but to a lesser degree than under unloading conditions. Nonlinear regression analyses indicated that the plantaris behaves like a slow-twitch muscle under unloading conditions and like a fast-twitch muscle when loaded. This suggests that the responses of these muscles to unloading and (or) Cb treatment might be influenced by factors beyond fiber type alone.