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It is well known that eye movements are influenced by an animal's state of arousal. Alterations in the dynamic characteristics of the horizontal vestibulo-ocular reflex of adolescent rhesus monkeys induced by changes in the animal's state of arousal were studied using linear system analysis employing both single frequency sinusoidal and white noise rotational stimulations. Arousal changes were induced by a behavioral task and/or the administration of amphetamines (0.5 mg/kg). Results indicate that highly alert animals display vestibulo-ocular reflex gains significantly different from less alert animals. Specifically, the gain of the vestibulo-ocular reflex is closer to unity over a wider range of frequencies in more alert animals. These changes were independent of the method used to maintain a high level of arousal.

In the frog's isolated head preparations, spontaneous activity was recorded from the whole nerve of the left horizontal semicircular canal (HC) for 6 min before and 16 min after destruction of the right labyrinth by heating or administration of d-tubocurarine (0.5 microliter, 5.10(-6)M) into the perilymph of the right labyrinth. Just after destruction on the right labyrinth, spontaneous activity of the left HC nerve abruptly increased by 20-400% in 24 preparations out of the 40 studied; activity then increased slowly and regularly and in most cases reached a steady level. In the 16 other preparations such destruction had no effect (15 preparations) or elicited a slight decrease of the HC nerve activity (one preparation). After curare administration, the spontaneous activity of the left HC nerve decreased by 20-100% in 27 preparations out of the 40 studied; in most cases such a decrease was reversed 25-80 min after administration of the drug. The spontaneous discharges were unaffected in 11 preparations and slightly increased in the two others. Destruction of the right labyrinth or administration of curare never modified spontaneous activity recorded from the left HC nerve when the connections between the two labyrinths had been interrupted either by sagittal section of the medulla oblongata or section of the right vestibular nerve close to the brain stem. These results demonstrate that one labyrinth has a tonic inhibitory influence on the contralateral one.

The differential effect of halothane on the characteristics of fast and slow components of vestibular nystagmus was investigated in rabbits. Eye movements were monitored using the "magnetic search coil" method and evaluated with the aid of a laboratory minicomputer. Low concentrations of halothane act preferentially on the fast component. There is a shift of the position threshold of fast component generation toward the periphery of the orbit and a diminution of the eye velocity during this nystagmus phase. Higher steady state concentrations of halothane reduced the velocity of the slow components whereby there is an increase in the amplitude of stimulation necessary to produce vestibulo-ocular responses of a magnitude to exceed the threshold of fast components. The results support the hypothesis that there are independent neural pathways for the production of fast and slow components of nystagmus whose neurons have different sensitivities to anesthetic agents.

Electrical responses to acoustic stimuli were measured by placing thin wire electrodes in the vestibular system of a pigeon model. Responses were measured after extirpation of the cochlea and the application of tetrodotoxin to the perilymphatic space. Responses seen were comparable to those of known cochlear microphonic potentials. These findings indicate that acoustic stimuli can evoke microphonic potentials in the vestibular system of the pigeon. We also found that vibrational amplitudes of less than 1 nm were sufficient to evoke a vestibular microphonic potential.

The behavior of single vestibular nerve fibers from the lateral semicircular canal was recorded during sinusoidal oscillations of the head, during optokinetic stimulation with the head stationary, and during spontaneous oculomotor behavior in the alert monkey. The response of similar fibers to adequate vestibular stimulation was also studied in some of the animals under deeply anesthetized conditions. In the alert animals all units were spontaneously active and their discharge was modulated only by adequate vestibular stimulation. Ipsilateral horizontal rotations of the head were excitatory for all units. No modification of this basic vestibular response by visual stimulation including full-field striped drum rotation was observed. Furthermore no correlation of unit activity with oculomotor function including voluntary saccadic and pursuit eye movements was found in any of the units. The regularity of spontaneous discharge was the most consistent characteristic that differentiated the unit response into types. Most units were very regular in discharge, but a few were very irregular. The averaging of unit discharge over several cycles of oscillatory head rotation showed that the irregular type units were also consistently modulated by adequate vestibular stimulation. Both regular and irregular type units were found in the anesthetized animals. Unimodal distributions of the quantitative values for unit resting discharge rate, sensitivity, and phase relationship were found. The distributions for these three parameters were similar in the units recorded in the anesthetized animals. Thus at least these characteristics of semicircular canal response seem not to be affected by the vestibular efferent system which should be altered or eliminated in the case of the anesthetized animals.

The morphological changes of the vestibular sensory epithelia and the vestibular ganglions induced by Gentamicin(GM) were investigated using scanning electron microscope, transmission electron microscope and light microscope. The guinea pigs were injected with a single application of 4 mg (0.1ml) of GM into the middle ear through the tympanic membrane. The vestibular organs and the ganglions were observed up to 6 months after the treatment. Four days after the injection, fused, ballooned and missing cilia were observed in the vestibular sensory epithelia. These changes progressed and extended toward the periphery of the crista and the macula. The changes of the vestibular ganglions were first observed one month after the treatment. The degenerative process started from destruction of the mitochondrial cristae and vacuolization of the cytoplasm in the Schwann cell. The next step of the change was dissociation of the myelin sheath around the ganglion cell. The cytoplasmic organelles in the ganglion cell gradually deteriorated. At the later stage, the myelin sheath around the ganglion cell disappeared and the number of the cell reduced. Furthermore, the myelin sheath of the nerve fiber was dissociated. In this study the signs of the vestibular ganglion damage were later than that of the vestibular organ. However, we thought the changes in the ganglion are probably due to direct influence of GM, since the degeneration was found to develop in a relatively short period.