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P Dallos

Publications and source records attributed to P Dallos.

At least 91 records · Page 5Linked to original sources

Intercellular communication in the supporting cells of the organ of Corti.

We have directly tested the concept that the supporting cells of the organ of Corti are functionally coupled through gap junctions. In vitro and in vivo preparations were evaluated. Electrical measurements clearly show that the cells are coupled ionically. Voltage drops measured in neighboring cells in response to intracellular current injections indicate that current spread decays rapidly. Despite the existence of electrical coupling, fluorescent dye injection studies revealed no dye spread into adjacent cells, other than a few instances which were clearly artifactual. However, it is possible that dye spread is very slow and that dye in adjacent cells is diluted below visual detectability. In any case, dye coupling is remarkably poor compared to other electrically coupled tissues. The role of coupling in the supporting cells may be nutritive, considering the avascular nature of Corti's organ.

Animals↗

Some electrical circuit properties of the organ of Corti. I. Analysis without reactive elements.

A simplified network model of the organ of Corti is analyzed with the assumption of parametric excitation via resistance changes in the hair cells' apical membrane. Pertinent network variables (intracellular resting and receptor potentials, cellular input resistance, extracellular potentials) depend on the ratios of basal (perilymphatic face) and apical (endolymphatic face) receptor cell resistances, denoted as shape factors. In the Appendix two methods are suggested for the computation of shape factors; both are based on the geometrical properties of hair cells. Various electrical quantities computed on the basis of shape factors are consistent with recent recordings from third turn inner and outer hair cells (Dallos et al. (1982): Science 218, 582-584). The model provides a plausible explanation for the experimentally observed discrepancy between inner and outer hair cell resting and receptor potentials. One potentially significant result of the analysis is the demonstration that since shape factors for outer hair cells are probably longitudinally graded, so must be all cellular electrical characteristics. Another interesting finding is that electrical interaction among neighboring hair cells is unlikely. A large-signal analysis of the circuit demonstrates that even in the absence of a non-linear input, the parametrically excited circuit itself generates pronounced distortion. The most significant consequence of this nonlinearity is a response asymmetry in which the depolarizing phase is greater than the hyperpolarizing one. Thus the circuit nonlinearity may, at least in part, account for the large positive d.c. response seen in both types of receptor cell (Dallos et al. (1982): Science 218, 582-584; Russell and Sellick (1978): J. Physiol. Lond. 284, 261-290).

Animals↗

Intracellular recordings from cochlear outer hair cells.

Intracellular recordings were made from outer hair cells in the third turn of the guinea pig cochlea, and the electrical characteristics of the cells were compared to those of inner hair cells, supporting cells, and extracellular spaces from the same recording region. Outer hair cells have higher membrane potentials than do inner hair cells, but they produce smaller a-c receptor potentials. The frequency response characteristics of both types of hair cells are probably not significantly different. In the frequency region where tuning is optimal, both cell types produce depolarizing d-c receptor potentials, but outer hair cells also generate hyperpolarizing responses at low frequencies.

Action Potentials↗

Two-tone interactions in the cochlear microphonic.

Two-tone interactions are explored for the cochlear microphonic (CM) in the guinea pig. Recordings are made from turns one and three using differential electrodes in the perilymphatic space or pipettes placed in scala media through a fenestra over the stria vascularis. We focus on magnitude changes associated with the introduction of appropriate interference tones and on various types of phase shift concomitant with these magnitude variations that have not received documentation in the literature. Based on extensive parametric data, it is suggested that some features of the gross interference phenomenon may be a consequence of the vectorial summation of outputs from contributing hair cell generators. These spatial effects appear to determine phase behavior and the influence of probe frequency on the frequency of maximal interference. In addition, the apparent interval between out defined best frequency (CF) and the frequency of maximal interference is most likely due to an underestimation of CF resulting from phase cancellation between CM-producing hair cell populations. However, after compensating for these spatial effects, several aspects of the CM interference phenomenon seem to be analogous to two-tone suppression in auditory nerve fibers. A direct one-to-one relationship is not implied since the latter reflect the outputs of inner hair cells while CM interference most likely reflects outer hair cell behavior. As a result, the association between suppression and interference must be sought in the process by which outer hair cell influence inner hair cell transduction.

Acoustic Stimulation↗

Psychophysical tuning curves and auditory thresholds after hair cell damage in the chinchilla.

Chinchillas were treated with kanamycin sulfate (150--200 mg/kg/day) to produce high-frequency hearing loss extending to about 4.0 kHz. Thresholds and psychophysical tuning curves (PTCs) were obtained before and after treatment, utilizing a shuttlebox avoidance procedure, and cochlear hair cells were evaluated under phase contrast microscopy. Hair cell loss resulting from kanamycin treatment varied from restricted lesions of the outer hair cells (OHCs) in the cochlear base, with no loss of inner hair cells (IHCs), to more extensive lesions involving both OHCs and IHCs. Threshold shift of at least 40 dB was always associated with OHC loss. PTCs obtained from frequency regions exhibiting 40--50 dB of threshold shift were normal in shape. With threshold shift in excess of 50 dB, PTCs were progressively distorted, with truncation of the tip segment and in some cases increased sensitivity of the tail segment. The results suggest that the threshold of optimally functional IHCs after kanamycin-induced OHC loss is about 40 dB higher than normal. Threshold shift in excess of 40 dB may represent IHC damage. IHCs are capable of transducing the fine-frequency information necessary for generating normally sharp PTCs in the absence of OHCs. However, with threshold shift in excess of approximately 50 dB, this frequency resolution is increasingly compromised.

Animals↗

Forward masking of auditory nerve fiber responses.

1. Responses of single fibers were obtained from the auditory nerve of chinchillas. Tone-burst stimuli consisted of a masking stimulus followed by a probe stimulus. Forward masking of a fiber's response is defined as a reduction in the magnitude of the probe-evoked response caused by the addition of the masking stimulus. 2. The recovery of probe response magnitude as a function of the time interval between masker offset and probe onset (delta T) follows an exponential time course. A relationship between the time course or magnitude of poststimulus recovery and the characteristic frequency (CF) of a fiber was not detected. 3. The iso-forward masking contour near the threshold of the masking effect across masker frequencies approximates a fiber's frequency threshold curve (FTC). In other words, forward masking tuning curves are essentially the same as frequency threshold curves. 4. The frequency dependence of forward masking is compared to that of two-tone suppression. Tonal stimuli outside the boundaries of a fiber's FTC that produce two-tone suppression are ineffective forward maskers. Certain frequency/intensity combinations within the FTC may produce both suppression and forward masking and tones within the remaining area of the FTC produce no suppression but are effective forward maskers. 5. Both the time course and the magnitude of the forward masking effect are dependent on the discharge rate evoked by the masker regardless of the masker's absolute level or spectral content. An increase in masker-evoked excitation causes an increase in time constant and a greater reduction in probe response magnitude, rd. The function relating rd to masker level parallels the firing rate/masker level function up to 40 dB above response threshold. 6. A decrease in masker duration from 100 ms leads to a decrease in both rd and the time constant of recovery. There is no significant difference between the 100 and 200 ms duration conditions. 7. Forward masking in single fibers is related to the period of poststimulus recovery of spontaneous activity, a component of a fiber's response pattern to the masker, and this component is tentatively identified as a period of recovery from short-term adaptation.

Adaptation, Physiological↗

Behavioral, compound action potential, and single unit thresholds: relationship in normal and abnormal ears.

Comparisons were made for two species (chinchilla and mongolian gerbil) among mean behavioral audiogram, mean just detectable action potential (AP) responses to tone bursts, and single-fiber response thresholds at the characteristic frequency, averaged in one-octave bands. In normal animals and in a group of Kayamycin-treated chinchillas, these mean measures appear to have a well-ordered relationship. Unit and AP thresholds are within 10 dB from one another throughout the frequency range. Behavioral thresholds are usually 15--20 dB more sensitive, but the three curves are roughly parallel except at the highest frequencies, where the behavioral threshold begins to increase approximately one-half octave above the physiological ones. Individual examples for four gerbils and four chinchillas having hair cell losses due to Kanamycin intoxication reinforce the notion based on mean data that in most cases AP thresholds can serve to predict the behavioral threshold configuration.

Action Potentials↗

Properties of auditory nerve responses in absence of outer hair cells.

1. Recordings were made from chinchilla auditory nerve fibers after portions of the cochlear outer hair cell (OHC) population were destroyed with the antibiotic kanamycin. In most cases the inner hair cell (IHC) population was completely preserved as determined by phase-contrast microscopy. We presume that the remaining IHCs are functionally normal, and thus that recordings obtained from fibers originating from the lesioned cochlear segment reflect IHC behavior. 2. Behavioral thresholds were measured for all animals both before and after the production of the cochlear lesion. The audiograms and the histological evaluation of the ears were the basis for assessing whether a particular fiber originated in a normal, pathological (shifted threshold; IHC only), or border region. These criteria also identified the animals that sustained IHC damage together with the destruction of part of the OHC population. Only the data obtained from those fibers which probably originated from the OHC-free segment of the cochlea are considered in detail. 3. Fibers whose characteristic frequency (CF) identified them as belonging to the normal (audiometrically and histologically) region, were found to be normal in all respects. 4. Fibers from the border region (where the audiogram has a steep slope between normal and hearing-loss regions probably corresponding to the segment where OHC loss progresses from less than 10% to more than 90%) had very complex response patterns. Their frequency threshold curves (FTC) showed great variability. In general, the closer the fiber was to the fully developed lesion, the more abnormal its FTC became. 5. Those units that were concluded to have originated from the OHC-free part of the cochlea could be divided into three categories on the basis of the shape of their FTCs. A small fraction had very broad tuning (9%). The majority (53%) had approximately normal tail segment, normal bandwidth of the tip segment, and highly elevated threshold at CF. A group of fibers (38%) could not be assigned a CF. Probably the FTC of most of these latter fibers are similar to those of the previous group, but the sharply tuned short tip segment was either missed or was not reachable on account of its extremely high threshold level. 6. Such indexes of fiber response as latency, spontaneous rate, and time pattern (PST histograms) were not affected by the loss of OHCs. 7. On the basis of the data and of the assumptions made it was suggested that outer hair cells provide a frequency-dependent sensitizing influence to the inner hair cells. The frequency dependence could best be expressed as a flat-topped band pass characteristic.

Acoustic Stimulation↗

Electrolytic lesioning in the cochlea.

A method has been developed whereby relatively discrete protions of the organ of Corti can be selectively destroyed with the use of a high-frequency current. The procedure involves passing th current (1 to 3 ma at an approximate frequency of 5 megahertz) between a differential pair of recording electrodes located in the scalae vestibuli and tympani of a particular cochlear turn. Damage patterns progressing from partial to complete outer hair cell lesioning and eventually to the inner hair cells accompanied by progressive decreases in cochlear microphonic sensitivity can be effected.

Animals↗