Search PubMed⌕ Search

Biomedical subjects

E S Luschei

Publications and source records attributed to E S Luschei.

At least 55 records · Page 3Linked to original sources

Morphologic alterations in Macaca mulatta following destruction of the motor nucleus of the trigeminal nerve.

In two adolescent male Macaca mulatta monkeys, small unilateral electrolytic lesions were produced in the motor nucleus of the trigeminal nerve. The side contralateral to the muscle paralysis served as the control side. The animals were killed 130 and 300 days postoperatively. One animal (animal A) was prepared as a dry skull preparation. Alterations in craniofacial form were noted clinically in both animals and included paralysis and atrophy of the muscles of mastication on the lesion side and mandibular asymmetry. In animal A (300 days postoperative survival), alterations in form included dental and mandibular asymmetry, the appearance of an anterior open-bite on the affected side, and a decrease in the size of the intratemporal fossa on the affected side. Remodeling changes were evident in the condylar process, the zygomatic arch, the orbit, and the zygomaticotemporal and zygomaticofrontal sutures on the lesion side but were not apparent on the contralateral side.

Animals↗

Cerebellar ablation and mastication in the guinea pig (Cavia porcellus).

The jaw movements of 3 subadult guinea pigs were recorded before and after cerebellar ablation with the aid of an optoelectronic tracking system. Despite overall ataxia of the animals' body and limbs, masticatory patterns were essentially normal. The major effects of cerebellar ablation upon Cavia mastication were a statistically significant (P < 0.01) increase in chew cycle duration and a decrease in chew duration variability.

Animals↗

Alterations in the facial skeleton of the guinea pig following a lesion of the trigeminal motor nucleus.

In thirty-three of sixty-six guinea pigs of the Topeka strain small, unilateral, electrolytic lesions were produced in the motor nucleus of the trigeminal nerve. Unoperated animals and the side contralateral to the muscle paralysis served as controls. Lesions were created when animals were 15 days or 75 days of age, and the animals were killed 15, 30, 45, or 60 days postoperatively. Each animal was subjected to dry skull preparations or radiographic and histologic techniques. Alterations in craniofacial form were noted in both the growing animals and the animals with little growth remaining. Alterations in form and function included paralysis and atrophy of the muscles of mastication on the lesion side, hypereruption of teeth, and reduction in growth of facial bones on the lesion side. Remodeling changes were evident in the glenoid fossa, the condylar process, and the coronoid process on the operated side but were not apparent in the contralateral control or the unoperated control animal.

Animals↗

Evidence that the human jaw stretch reflex increases the resistance of the mandible to small displacements.

1. Small 'step' or sinusoidal displacements were imposed on the mandible while human subjects maintained an average biting force of 10 N. Phase-related changes in the force resisting sinusoidal displacement were used to determine the mechanical stiffness of the human mandibular system as a function of the frequency of stretching. 2. Jaw-muscle electromyographic (e.m.g.) responses to 'step' stretches were of 8 msec latency and generated a very substantial force response. Jaw-muscle e.m.g. responses having longer latency were not observed. 3. The mechanical stiffness of the human mandible was relatively constant as a function of the frequency of stretching, having a typical magnitude of about 15 N/mm (+/- 200 micrometers stretch) or 10 N/mm (+/- 1500 micrometers stretch) at mean biting forces of 10 N. The force resisting displacement was phase-advanced at all frequencies. 4. Modulation of jaw muscle electrical activity evoked by sinusoidal stretches increased in amplitude as a function of increasing stretch frequency. E.m.g. modulation was 60--100 degrees advanced at frequencies of 1--10 Hz, but the phase decreased at higher frequencies, becoming negative (lagging stretch) at frequencies of 30 Hz and above. These characteristics are consistent with the idea that the jaw stretch reflex is dependent on jaw muscle spindle afferent fibres exciting jaw-closing motoneurones by relatively direct (but not necessarily monosynaptic) connexions. 5. The relationship between jaw-muscle activity and voluntary fluctuations of isometric biting force suggests that human jaw muscles can be modelled as a second-order linear 'filter'. The corner frequency for human jaw muscle is about 3 Hz; thus it would appear to be considerably slower than jaw muscle of monkeys. 6. The reflex stiffness of the human mandible, estimated quantitatively on the assumption that human jaw muscle stiffness is similar to the intrinsic stiffness of the gastrocnemius of the cat, ranges between 5 and 9 N/mm at frequencies between 1 and 8 Hz. Since this reflex stiffness is about the same as muscle stiffness in this frequency range, we conclude that the stretch reflex of the human mandible contributes functionally to its postural stability. 7. Reflex stiffness appears to be greater in the monkey mandible relative to muscle stiffness than in the human mandible. The difference is argued to be a manifestation of the difference in jaw muscle contraction speed between the two species. 8. The fact that the mandibular stretch reflex appears to be stronger than the stretch reflex of the limbs of intact animals and humans is discussed in terms of the special anatomical and functional features of the mandible.

Adult↗

Temporomandibular joint meniscectomy--effects on joint structure and masticatory function in macaca fascicularis.

The postoperative effects of unilateral temporomandibular joint meniscectomy on joint structure and masticatory function were evaluated in four mature Macaca fascicularis and compared with one control. Mandibular movement during mastication was monitored objectively with an optoelectronic tracking system within four months and again within twelve months postmeniscectomy in each animal. Temporomandibular joint structure was documented radiographically and histologically. Results showed that degenerative joint disease was produced in the postsurgical joint, and that the morphological changes were location-dependent. Fibrous ankylosis was observed histologically in three animals. The contralateral joints were not affected morphologically, except for bony resorption of the articular eminence noted microscopically in one animal. Radiographically, however, the joint appeared normal. Variable alterations in masticatory patterns were observed following unilateral meniscectomy. While there appeared to be an association between temporomandibular joint structure and masticatory function, radiographic and microscopic observation of morphological alterations in the joint did not result in predictable functional limitations in chewing pattern.

Animals↗

The strength of the reflex response to sinusoidal stretch of monkey jaw closing muscles during voluntary contraction.

1. Rhesus monkeys were trained to exert steady biting forces of 3--60 N for 1--2 sec. This behaviour was well maintained while sinusoidal or step opening and closing movements were imposed on the jaw. 2. The amplitude of the force modulation during sinusoidal stretching was divided by the amplitude of movement to obtain the magnitude of stiffness. This estimate was made at frequencies from 2 to 50 Hz at amplitudes of 100 and 500 micrometer (half the peak-to-peak movement at the incisors). 3. Peak magnitudes of stiffness were seen with frequencies of 8--15 Hz when the amplitude of movement was small; there was a great deal of variation between individual animals. This variation was most striking with mean forces of 25--35 N. The stiffness was greatest in animals that showed considerable spontaneous tremor, and the highest levels of stiffness were often recorded with frequencies near which tremor amplitude was large. A marked phase lag in the force response was often seen during small amplitude stretching at 8--30 Hz. 4. Estimates of stiffness for larger amplitude (500 micrometer) stretching showed less variation; the magnitude of stiffness showed maximum values below 10 Hz and a minimum at 15--30 Hz. Force always showed a phase lead on position although this lead became small in the frequency range where with smaller movement there had been phase lags. The magnitude of stiffness increased with increasing mean force. 5. Bilateral electrolytic lesions were made in the brain stems of three animals; they reduced by over 95% the expected number of cells in the mesencephalic nucleus of the fifth cranial nerve on either side. These lesions interrupted the afferent pathway for the stretch reflex and so abolished excitatory electromyogram (e.m.g.) responses to step stretches of the jaw closing muscles. 6. Such reflex responses as persisted after the lesions were small and inhibitory. E.m.g. silences followed both step stretch and release; the response to release was a 'load compensation' that could not be attributed to spindle afferents. 7. After the lesions the responses to movements of 100 micrometer showed neither negative values for the phase nor marked peaks in the stiffness magnitude at low frequencies; these features therefore take origin in the action of the stretch reflex. The stiffness that was measured after the lesions may be attributed to the non-reflex components resisting stretch, particularly to the properties of the contracting muscles. Thus, the phase of the force response was markedly advanced at all frequencies and the stiffness seen for 100 micrometer was similar to that for 500 micrometer. Stiffness increased with increasing mean force, as before surgery. 8. Vector subtraction of the stiffness seen at each frequency after interrupting the stretch reflex from that seen before doing so gave a quantitative estimate of the strength of the stretch reflex. The reflex activity calculated in this way showed attenuation and progressive phase lag as the frequency increased above 10 Hz...

Afferent Pathways↗

Role of monkey precentral cortex in control of voluntary jaw movements.

Monkeys were trained to produce a low, steady biting force for 0.5-2.5 s, and then a rapid forceful bite in response to a visual stimulus. After large bilateral lesions of the precentral face area, monkeys emitted repetitive forceful bites on the apparatus, but could not perform the force-holding task. They eventually relearned the task, but the force exerted was never as steady as it was prelesion, and often oscillated at about 2 and/or 5-6 Hz. After retraining, two animals with large bilateral lesions of the face area produced median RT responses equal to or only slightly longer than their prelesion performance, indicating that neural pathways not involving the precentral cortex can mediate quick visual RT responses. The variability of RTs was permanently increased, probably as a result of the persistent unsteadiness of the force-holding response. Incomplete bilateral lesions of the precentral face area, a complete unilateral lesion of that area, and bilateral lesions adjacent regions of cortex produced either mild, transient difficulties with the biting taks, or no problems at all. The results indicate that the precentral cortex has a role in the control of voluntary jaw movements. Lesions caused difficulty in controlling, but not producing, closing jaw movements, thereby suggesting that this role is predominantly to inhibit jaw-closing motoneurons or the systems that excite them. Electrical stimulation studies of the face area of the precentral cortex of the unanesthetized monkey point to the same conclusion.

Animals↗

Discharge of spindle afferents from jaw-closing muscles during chewing in alert monkeys.

The discharge of muscle spindle afferents from monkey spindle afferents from monkey jaw-closing muscles was studied during mastication of natural foods by extracellular recording from the fibers or cell bodies of the tract and mesencephalic nucleus of the fifth nerve. In all, 39 muscle afferents were studied. The spindle associated with 18 of the afferents was positively identified by the afferent's response to gentle, localized palpation of either the temporalis or masseter muscle. Discharge patterns were observed during mastication, and in the majority of cases the qualitative passive response characteristics of the spindle afferent were determined. During steady chewing spindle afferent discharge typically paused briefly during the initial rapid upward part of the chewing cycle. Firing generally began as the jaw slowed its upward movement, and firing rates during the slow grinding portion of the upward movement were within the range of 50-80 spikes/s. All spindles exhibited a brisk discharge during the opening movement, typically within the range of 100-150 spikes/s. One-third of the spindle afferents exhibited a brief, high-frequency burst of firing at the very beginning of the opening movement, presumably as a result of stretch applied to a spindle just previously subjects to fusimotor excitation. Although the results of the study make it clear that spindles in jaw-closing muscles are coactived along with the extrafusal muscle fibers, the fusimotor bias does not seem capable of sustaining discharge in the face of rapid shortening of the muscle. Furthermore, the fact that discharge rate during opening, when the jaw-closing motoneurons are quiescent, is much higher than at any part of the closing cycle, when the motoneurons are active, suggests that the muscle spindles cannot provide the primary excitatory drive to the motoneurons.

Acoustic Stimulation↗

Increases in reflex excitability of monkey masseter motoneurons before a jaw-bite reaction-time response.

Reflex excitability of the motoneurons innervating the masseter muscle of monkeys was tested before a phasic voluntary activation of the jaw-closing muscles (a RT bite response). Single test shocks were delivered to the Mes V which supplies a monosynaptic excitatory input to the jaw-muscle motoneurons. Changes in reflex excitability were assessed by measuring the amplitude of the synchronous muscle potential evoked by the test shock. Amplitudes of the muscle potentials evoked by shocks which occurred just before the beginning of the voluntary EMG response, as judged by the onset of EMG activity of the masseter muscle contralateral to the test shock were many times larger than potentials evoked immediately following the visual RT stimulus. Curves relating the average amplitude of the evoked response to its time before the beginning of the voluntary response suggest that the reflex excitability of the motoneuron pool begins to increase 25-45 ms before the first detectable EMG activity occurs. These results suggest that inputs arrive at the motoneurons of agonist muscles used in rapid RT tasks substantially before changes in the EMG of the muscle are noted. These results, in part, would account for the time interval noted between the beginning of neural activity in suprasegmental structures which presumably excites spinal motoneurons, and the first EMG activity of muscles which are innervated by these motoneurons.

Animals↗

Variability of neuropathologic lesions in experimental methylmercurial encephalopathy in primates.

Acute and chronic intoxications of rhesus monkeys with methylmercury produced lesions in the central nervous system (CNS) with different distributions. Neuronal degeneration and astroglial proliferation predominated in the dentate nucleus, lateral geniculate nucleus, thalamus and pontine nuclei in 2 monkeys that received 2 mg/kg/day for 17 and 18 days, whereas pseudolaminar necrosis and astroglial proliferation were observed in the cerebral crotex, maximally in the calcarine and insular regions, in 4 monkeys that received 0.5 to 0.8 mg/kg/day for 3 to 8.5 months. Mercury concentrations in the CNS were much higher in the acutely intoxicated animals than in the chronically intoxicated animals, but the correlation between concentrations of mercury and the histologic destruction was not precise.

Animals↗