"Saccadic nystagmus" in cerebellar cortical atrophy.

An ocular dyskinesia designated "saccadic nystagmus" was observed in a patient with cerebellar cortical atrophy. Saccadic nystagmus is a sustained ocular dyskinesia present during visual fixation and abolished by eye closure. It is difficult to distinguish visually from either pendular or jerk nystagmus without eye movement recordings. The oscillations are horizontal and rapid and may be influenced by direction of gaze. Caloric nystagmus (eye closed) and optokinetic nystagmus were normal in our patient. Visual fixation abolished caloric nystagmus, which was replaced by saccadic nystagmus.

Compound action potentials and single unit responses to a 1 kHz haversine in the cat.

The single-cycle 1 kHz haversine (one cycle of a 1 kHz sine wave beginning at -90 degrees) is a low-frequency impulsive stimulus which has been little use, but which has significant potential applications both as a clinical and a research tool. The auditory nerve compound action potential (CAP) and single unit discharge patterns evoked by a single-cycle 1 kHz haversine stimulus were studied in anesthetized cats. The haversine CAP waveform consisted of two or three short latency peaks with peak to peak intervals of about 1.0 ms. Latencies of the CAP peaks decreased with increased stimulus intensity and were also strongly dependent on stimulus polarity. Typically, CAP peak latencies changed by about 0.5 ms with stimulus polarity reversal. Single unit responses were classified by the peak latency pattern of their haversine post-stimulus time histograms (PSTHs). Low CF units had low thresholds and PSTHs resembling their click responses. High CF units had high thresholds and PSTHs comprised of one or two short latency peaks whose latencies were polarity-sensitive. Some units in an intermediate CF range (approximately 1.5-3.0 kHz) had PSTHs which were a transitional form between the high and low CF types of response. The unit discharge patterns strongly suggested a low frequency origin for the haversine CAP at all intensities.

Spontaneous, click-, and toneburst-evoked otoacoustic emissions from normal ears.

Evoked and spontaneous otoacoustic emissions were recorded bilaterally in a group of normal subjects (n = 14) using clicks and tonebursts at four frequencies (0.5, 1, 1.5, and 3 kHz). All ears (n = 28) demonstrated evoked emissions, but not to every stimulus type. The 0.5-kHz toneburst evoked emissions in only 10 (36%) ears, the 1.5-kHz toneburst in all ears, and the remaining stimuli in at least 80% of ears. Two distinct patterns of evoked emissions were identified. Five (18%) ears showed short, broadband click-evoked emissions lasting less than 20 ms after stimulus onset. In these ears, toneburst-evoked emissions were often more prominent than click-evoked emissions and no spontaneous emissions were detected. Twenty-three (82%) ears showed click-evoked emissions lasting longer than 20 ms poststimulus onset. Spectral analysis of these emissions demonstrated several (2-10) narrow frequency peaks. Highly similar peaks were present in the spectra of toneburst-evoked emissions within the range of toneburst spectra. Spontaneous emissions were recorded in 12 of the 23 ears. In these ears, at the frequencies of spontaneous emissions, prominent peaks in both click- and toneburst-evoked emission spectra were always present. Otoacoustic emission characteristics correlated significantly between the ears of individual subjects inferring that a symmetrical cochlear mechanism generates otoacoustic emissions.

Spontaneous otoacoustic emissions in the nonhuman primate: a survey.

A number of reports have described a relatively high incidence of spontaneous otoacoustic emissions (SOAEs) in recordings made from the sealed human ear canal. Our attempt to detect similar emissions in 122 presumably normal-hearing ears from 61 monkeys revealed SOAEs in 5% of the primates and 2.5% of the ears tested.

Acoustic distortion products in rabbit ear canal. I. Basic features and physiological vulnerability.

In contrast to evoked otoacoustic emissions, acoustic distortion products (DPs) recorded from the ear canal are present at predictable frequencies with respect to their primary tones, f1 and f2. Such specificity may provide detailed frequency-place information concerning the functional state of limited regions of the organ of Corti following experimental intervention. However, to date, it is not clear whether emitted DPs solely reflect activity at the basilar-membrane regions of primary tones or if the remote DP site makes a significant contribution to the emitted signal measured in the ear canal. We have investigated a number of the general features of acoustic-DP generation in the rabbit so that, in later experiments, the contributions of specific basilar-membrane regions involved in generating these DPs can be identified using techniques designed to manipulate their normal properties. The first report describes the outcome of systematic manipulations of a number of stimulus conditions and alterations to the physiological state of the cochlea by exposure to fatiguing sound or anoxia. Experimental findings for the 2f1-f2 DP showed that, in general, the relations of the levels and frequency of the primary tones to DP magnitude were consistent with previously published data from other mammalian species. Additional observations for other odd-order intermodulation DPs at the 3f1-2f2 and 2f2-f1 frequencies suggested that the basic attributes of the acoustic DPs were similarly affected by systematic manipulation of the basic parameters of the primary tones and the general metabolic state of the cochlea. General anesthesia, however, did not affect DP amplitude. A companion paper describes the results of a series of subsequent experiments using response-suppression, interfering-tone, and temporary threshold shift techniques which address more directly the issue of which basilar-membrane sites contribute to the generation of different acoustic DPs.

Acoustic distortion products in rabbit ear canal. II. Sites of origin revealed by suppression contours and pure-tone exposures.

Previous work on acoustic distortion products (DPs) recorded from the ear canal has not established unequivocally whether emitted DPs principally reflect basilar-membrane nonlinearities at the frequency sites of the primary tones, f1 and f2, or if the DP-frequency place itself makes a significant contribution to the emitted response. Results from some studies on acoustic emissions attribute generation of the emitted DP almost exclusively to the regions of maximum primary-tone interaction, while the findings of other investigations implicate reemission of the response from the DP locus as a significant contributor to response magnitude. Using suppression, interfering tones, and temporary threshold shift (TTS) procedures, the work reported here was designed to establish more definitively the precise contributions of the basilar-membrane regions involved in generating acoustic DPs in rabbits. Suppression tuning curves and interfering-tone experiments indicated that for the DP at 2f1-f2, regions near the f1 or f2 frequencies were the major contributors to the emitted response. However, for the higher-frequency DP at 2f2-f1, the basilar-membrane region just basal to the DP site was implicated as the generator. Following brief episodes of TTS at frequencies related to either the DP or the primary tones, the locus of the exposure stimulus that most effectively reduced the magnitude of the 2f1-f2 response also implicated the region of maximal primary-tone interaction in the generation of the acoustic DP. In contrast, for the DP at 2f2-f1, basilar-membrane sites nearer the DP were identified as the primary contributors to the emitted response. Both sets of results imply that different DPs recorded from the ear canal may originate from unique regions of primary-tone interaction along the basilar membrane.

Spontaneous otoacoustic emissions in a nonhuman primate. I. Basic features and relations to other emissions.

Otoacoustic emissions in both ears of a rhesus monkey exhibiting stable spontaneous emissions (SOEs) were monitored over a 1-year period. The amplitudes and frequencies of both SOEs and stimulus-frequency emissions (SFEs) were routinely recorded, while transiently evoked (EOE) and distortion-product emissions (DPEs), at the frequency 2f1-f2, were occasionally examined. Between evaluation sessions, both the frequencies and amplitudes of SFEs remained relatively stable in both ears, while the frequencies and amplitudes of SOEs were less constant. Isosuppression contours for SOEs, plotted as a function of frequency and level of tonal maskers, revealed sharp tuning consistent with normal frequency selectivity. Detailed analyses of long-term measurements showed that SOEs occurred most frequently at the peaks of the SFE response. A regular frequency spacing between neighboring amplitude maxima and minima of the SFEs was consistent with the notion that this particular emitted response may result from a periodic disruption of the orderly pattern of sensory cells along the organ of Corti. Intramuscular administration of aspirin abolished SOE and SFE responses, while DPEs remained relatively unchanged suggesting the involvement of separate mechanisms in the generation of different emissions.

Spontaneous otoacoustic emissions in a nonhuman primate. II. Cochlear anatomy.

Both cochleas of a rhesus monkey exhibiting stable spontaneous and stimulus-frequency emissions were evaluated histologically using surface-preparation methods to determine if certain features of these emissions could be related to structural properties of the organ of Corti (OC). The comprehensive assessment included preparation of routine cytocochleograms and a detailed study of the arrangement of cochlear sensory cells, best revealed by the precise positional relationships between stereocilia bundles, in selected areas representing low-, medium-, and high-frequencies. Several additional measurements were made in an area extending from about 25-60% distance from the apex, which was estimated to encompass the cochlear region where emissions were generated. These quantifications included measures, in both micrometers and Hertz, of the distances between irregularities in the lateral border of the OC due to a sporadically occurring fourth row of outer hair cells (OHCs). Measures, in micrometers, of the changes in the radial extent of the corresponding OC in the presence or absence of this extra fourth row of OHCs were also made. A final measure within low-, medium-, and high-frequency OC regions consisted of describing the angles that the tips of the stereocilia bundles were displaced from an axis parallel to the tunnel of Corti. For comparative purposes, similar plots were made in comparable regions of the OC in the normal and experimental cochleas of three additional rhesus monkeys in which one ear had been systematically exposed to noise. In the emitting-monkey cochlea, there was a mild loss of sensory cells scattered throughout the OC which was generally greater for the OHCs. No evidence of small circumscribed lesions, defined as a loss of more than four adjacent hair cells, was found. The most striking observation which varied in degree across the three other monkeys was a generalized irregularity in the cellular organization of the OHC region which was most pronounced in the low- and midfrequency regions of the OC. The notable cellular disorganization specific to the apical half of the cochlea was reflected by an increased variance in the distribution of deviation angles measured for corresponding stereocilia bundles. Outer hair cells in the remaining basal region of the OC were arranged in three regular rows with the usual stereocilia orientation.(ABSTRACT TRUNCATED AT 400 WORDS)

The normal summating potential recorded from external ear canal.

With a "plastic leaf" electrode, cochlear summating potential (SP) and auditory nerve action potential (AP) responses to rectangular-pulse clicks were recorded from the ear canal skin surface of 96 normal-hearing ears of 48 subjects. The main goals of this investigation were to develop a more precise characterization of the relationship between SP and AP amplitudes across normal ears and to determine the confidence limits of this relationship so that a more accurate "normal limit" could be established for clinical testing. The results suggest that the across-subjects SP-AP amplitude relationship is linear. Also, SP scatter increases as AP amplitude increases, but the scatter is equalized by log transforming the data. The distance of the SP from the log-transformed SP-AP estimating line in SE ("AP-normalized SP amplitude") was found to be superior to the SP/AP amplitude ratio as a method of adjusting SP to AP amplitude, because the SP/AP ratio varied significantly with AP amplitude both across subjects and with different ear canal electrode positions.

Immersed false vertical room. A new motion sickness model.

We evaluated a new model of motion sickness--an enclosure decorated with visual cues to upright which was immersed either inverted or "front"-wall down, in Johnson Space Center's Weightless Environment Training Facility (WETF) pool. This "WETF False Vertical Room" (WFVR) was tested with 19 male and 3 female SCUBA diver subjects, aged 23 to 57, who alternately set clocks mounted near the room's 8 corners and made exaggerated pitch head movements. We found that (1) the WFVR test runs produced motion sickness symptoms in 56% and 36% of subjects in the room-inverted and room-front-down positions, respectively. (2) Pitch head movements were the most provocative acts, followed closely by setting the clocks--particularly when a clock face filled the visual field. (3) When measured with a self-ranking questionnaire, terrestrial motion sickness susceptibility correlated strongly (P < 0.005) with WFVR sickness susceptibility. (4) Standing instability, measured with a modified Fregly-Graybiel floor battery, also correlated strongly (P < 0.005) with WFVR sickness susceptibility. This result may reflect a relationship between visual dominance and WFVR sickness. (5) A control study demonstrated that the inverted and front-down positions produced WFVR sickness, but the upright position did not, and that adaptation may have occurred in some subjects with repeated exposure. The WFVR could become a useful terrestrial model of space motion sickness (SMS) because it duplicates the nature of the gravity-dependent sensory conflicts created by microgravity (visual and otolith inputs conflict while somatosensory gravity cues are minimized), and it also duplicates the nature of the provocative stimulus (sensory environment "rule change" versus application of motion to passive subject) more closely than any other proposed terrestrial SMS model. Also, unlike any other proposed terrestrial SMS model, the WFVR incorporates whole-body movement in all three spatial dimensions. However, the WFVR's sensory environment differs from that created by spaceflight in several respects, including the presence of frictional drag on limb movement, magnification at the face-mask-water interface, greater otolith conflict, exhaled bubbles, and the presence of some gravity-dependent somatosensory inputs.

Inverted immersion as a novel gravitoinertial environment.

BACKGROUND: Inverted immersion (II) offers a unique opportunity to swing the orientation of the gravity vector 180 degrees from its usual configuration with vestibular end organs. During II, extrathoracic fluid dynamics are identical to those of upright immersion (UI). II exposes individuals to a novel gravitoinertial environment and, therefore, should produce motion sickness (MS). HYPOTHESIS: II is more provocative of signs and symptoms of MS than UI. METHODS: Nine subjects were exposed once to II and UI. Conventional SCUBA gear was worn. In II, the subject wore a wetsuit which provided 5-7 kg force of positive buoyancy and, with no weight belt, caused him to float while inverted against the underside of a platform. An experiment with UI was identical except that a weight belt was worn which provided 5-7 kg force of negative buoyancy, and the subject stood upright against the bottom of the pool. The experiment was terminated after 3 hours or "upon the onset of the first, clear, persistent feeling of nausea", whichever came first. Throughout the experiment the subject rotated through a series of tasks: assembly of a pipe puzzle, performance of a series of head movements, and ambulation. Immediately post-dive, postural stability was assessed with tandem standing with and without eyes closed and with and without the neck extended 45 degrees. A questionnaire regarding susceptibility to motion sickness was completed pre-dive. RESULTS: No subject terminated the test because of MS during UI; seven subjects terminated the test during II (p < 0.025, McNemar's test). Posture was less stable after II than after UI (p < 0.05, sign test). MS questionnaire results did not predict susceptibility to II. CONCLUSION: II is provocative of MS and postural instability.