A desnutrição proteico-calórica é um dos maiores problemas de saúde pública no Brasil, especialmente no Nordeste, acometendo, com maior frequência, crianças pré-escolares e determinando possíveis comprometimentos, não só no crescimento ponderal como intelectual e cognitivo, podendo ocasionar déficits irreversíveis, dependendo da sua intensidade e duração. Considerando-se a importância da integridade anatomofisiológica do sistema auditivo periférico e central para o adequado desenvolvimento da plenitude das habilidades auditivas, de linguagem e aquisição de aprendizagem, torna-se fundamental a reflexão sobre os possíveis efeitos deletérios da desnutrição no sistema nervoso auditivo, para que possíveis anormalidades auditivas sejam identificadas e tratadas nessa população. O objetivo deste estudo foi caracterizar as respostas do Potencial Evocado Auditivo de Tronco Encefálico, com estímulos clique e tone burst, em crianças de zero a 60 meses, desnutridas e eutróficas, com função auditiva periférica íntegra, bem como compará-las. Foram examinadas 111 crianças de zero a 60 meses, sendo 57 desnutridas e 54 normonutridas, com avaliação otorrinolaringológica, imitanciometria e Emissões Otoacústicas Evocadas Transientes dentro dos padrões de normalidade. A seguir, os Potenciais Evocados Auditivos do Tronco Encefálico por estímulo clique e tone burst foram registrados. Na análise dos dados, observou-se que as latências das ondas I, III e V e dos interpicos III-V a 80 dBNA com estímulo clique eram significativamente maiores em crianças desnutridas, quando comparadas às eutróficas, assim como do intervalo I-V na faixa etária de 0-24 meses. As latências da onda V nas intensidades de 60, 40 e 30 dBNA também foram significativamente maiores em crianças desnutridas. Na análise do Potencial Evocado Auditivo de Tronco Encefálico tone burst, a onda V mostrou latência maior nas crianças desnutridas em todas as intensidades e frequências testadas, entretanto, essa diferença nas crianças de zero a 24 meses só foi significativa em 2000 Hz; nas de 25 a 60 meses foi significativa apenas em 500 Hz a 80 dBNA, em 2000 Hz a 30 dBNA e em 4000 Hz a 60, 40 e 30 dBNA. Crianças desnutridas apresentaram alterações no Potencial Evocado Auditivo do Tronco Encefálico, caracterizadas pelo atraso na latência das ondas e dos intervalos interpicos, quando comparadas às eutróficas, sugerindo déficit de condução na via auditiva. Sendo assim, concluiu-se que a desnutrição pode provocar efeitos deletérios no processo de desenvolvimento e maturação do sistema nervoso auditivo. / Introduction: protein calorie malnutrition is one of the biggest public health problems in Brazil, especially in the northeast, affecting most often preschool children and determining possible compromises not only the weight growth but also intellectual and cognitive development, which may cause irreversible deficit, depending on its intensity and duration. Considering the importance of anatomical and physiological integrity of the peripheral and central auditory system for the proper development of the fullness of auditory skills, language, and acquisition of learning, this brings out a fundamental reflection over the possible deleterious effects of malnutrition in the auditory nervous system, so that possible auditory abnormalities are identified and addressed in this population. The objective of this study was to characterize the response of the auditory brainstem evoked potentials test with click and tone burst stimuli in malnourished and eutrophic children from 0 to 60 months of age, with normal peripheral auditory function, as well as to compare them. Casuistic and Method: One hundred and eleven children from 0 to 60 months of age were examined, being 57 malnourished and 54 eutrophic. They underwent ENT evaluation, including impedanciometry and transient evoked otoacoustic emission (TEOAE) being those within normal ranges. Folowing, the auditory brainstem evoked potentials with click and tone burst were registered in the intensity of 80, 60, 40 and 30 dBNA. Results: In the analysis of the results, the latencies of waves I, III and V and the interpeak III-V 80 dBNA latencies with click stimuli were significantly higher in all malnourished children, when compared to the eutrophic children, as well as I-V interpeak interval in the 0-24 months of age group. The wave V in 60, 40 and 30 dBNA latencies were also significantly higher in malnourished children. In the analysis of the tone burst auditory brainstem evoked potentials wave V latency showed higher in malnourished children in all intensities and frequencies tested, however this difference in children from 0-24 months were significant only in 2000 Hz; in children from 25-60 months were significant only at 500 Hz to 80 dBHL, in 2000 Hz at 30 dBHL and 4000 Hz to 60, 40, and 30 dBHL.Malnourished children present a higher range of alterations in auditory brainstem evoked potentials, characterized by delayed wave latencies and higher interpeak intervals when compared with eutrophic children, suggesting a peripheral and central deficit in the auditory pathway, thus concluded that malnutrition may cause deleterious effects in the development and maturation of the auditory nervous system.

Nonlinear frequency compression is a signal processing technique used to increase the audibility of high frequency speech sounds for hearing aid users with sloping, high frequency hearing loss. However, excessive compression ratios may reduce spectral contrast between sounds and negatively impact speech perception. This is of particular concern in infants and young children, who may not be able to provide feedback about frequency compression settings. This study explores use of an objective cortical auditory evoked potential that is sensitive to changes in spectral contrast, the auditory change complex (ACC), in the verification of frequency compression parameters. We recorded ACC responses in adult listeners to a spectral ripple contrast stimulus processed with a range of frequency compression ratios (1:1 to 4:1). Vowel identification, consonant identification, speech recognition in noise (QuickSIN), and behavioral ripple discrimination thresholds were also measured under identical frequency compression conditions. In Experiment 1, these measures were completed in ten adult normal hearing individuals to determine the effects of this type of signal processing in individuals with optimal hearing. In Experiment 2, these same measures were repeated in ten adults with sloping, high frequency hearing loss, which is the clinical population for whom this signal processing technique was intended. No significant relationship of compression ratio and vowel identification was found in the normal hearing listeners, though a significant negative effect of increasing frequency compression ratio was observed in the hearing impaired group. Significant effects of compression ratio on ACC amplitude, consonant identification, ripple discrimination threshold, and speech perception in noise were found for both the normal hearing and hearing impaired groups. These results indicate that the ACC response, like speech and non-speech perceptual measures, is sensitive to frequency compression ratio. Further investigation of this technique with hearing impaired individuals is needed to determine optimal stimulus and recording parameters for the ACC in both adults and children.

his study compared auditory behavioral and physiological measures among three subject groups: 1) Normal control subjects, 2) subjects who were on a prescribed SSRI for depression, and 3) subjects who were prescribed an SSRI for depression, but were not medicated at the time of testing. Test measures included: Standard audiological tests (audiometry and tympanometry), electrophysiological procedures for analysis of auditory- evoked brainstem and late responses, and standardized behavioral speech tests (SCAN-A, SSI, and the low predictability sentence list of the R-SPIN). Analysis of results indicated a statistically significant increase of group mean amplitude of the ABR peak V, from 15dBnSL to 55dBnSL, in the non-medicated group compared to controls. Also, the non-medicated group scored significantly less favorably than controls on the most challenging listening condition (-20 MCR) of the SSI, in the left ear. Although other test measures indicated consistent differences between these two groups, they were not, however, significant.

This work examines somatosensory processing in "giant" neurones of the medial pontomedullary reticular formation (PMRF) in the rat, with particular emphasis on the response to cutaneous thermal stimuli. Thermal test stimuli were employed as these were deemed to be more precisely quantifiable than other forms of cutaneous stimulation. Activity was recorded from 235 PMRF neurones in 94 female Long Evans rats (270 to 320 g) anaesthetised with urethane (1,25g/kg, i.p.). Rectal temperature was closely controlled at 38 ± 0,5°C. Standard stereotactic and extracellular recording techniques were employed. PMRF giant neurones were identified by their stereotactic location, large, stable spike amplitudes of long duration, responses to cutaneous mechanical stimuli and receptive field properties, and spontaneous discharge characteristics. Ramp, step and sine wave cutaneous thermal stimuli (35-48 °C) were applied to the glabrous skin on the hindpaw by means of a computer-controlled Peltier device. The location of the units was confirmed by subsequent histology. One hundred and eleven neurones were located in nucleus reticularis pontis caudalis (NPC), and 124 in nucleus reticularis gigantocellularis (NGC). Mechanical stimulation excited 188 of 235 (80%) PMRF neurones (ON-m cells), and inhibited 40 (17%, OFF-m cells). Seven cells (3%) had mosaic receptive fields of excitation and inhibition (complex responses, CX-m). Twenty-eight percent of neurones were responsive to both weak and intense stimuli (mixed neurones). The remainder (72%) responded only to intense mechanical stimulation of the skin (high threshold neurones). The (excitatory or inhibitory) response of the mixed neurones to intense stimuli was generally greater than to mild stimuli, Receptive fields ranged in size from restricted (hindlimbs only) to very extensive (covering the entire body surface). Neurones with small receptive fields were almost exclusively of the high threshold type, and tended to be located in NGC, while mixed neurones tended to have larger receptive fields, and were located predominantly in NPC. Some portion of the hind limbs were represented in the receptive fields of all but one of the neurones studied, while the tail and/ or trunk were represented in 77%, and the forelimbs and face in 28% of receptive fields. Most of the cells responding to cutaneous mechanical stimulation had bilateral (usually symmetric) receptive fields. Spontaneous (background) activity occurred in the absence of any deliberate sensory stimulation in 72% of PMRF neurones. The frequency of spontaneous discharge rates ranged from O to 47 spikes/ s. The coefficient of variation of the spontaneous discharge rate of a given neurone was generally less than 20% (range O to 85%). Of the 235 identified mechanosensitive PMRF neurones, 203 (86%) also responded to cutaneous thermal stimulation (43-48 °C) of the ipsilateral hind paw. Eighty percent of these responded with increased discharge rates (ON-t cells), and 20% were inhibited (OFF-t cells). The polarities of response of individual PMRF neurones to mechanical and thermal stimuli, and to repeated ipsilateral and contralateral thermal stimuli, did not differ significantly. Following transient thermal stimulation, spontaneous discharge rates largely returned to pre-stimulus levels. The thresholds of response to slow ramp (0,15°C/s) and stepped (2°C/s) thermal stimuli occurred both in the innocuous and noxious temperature ranges (below and above 42°C, respectively). The threshold temperatures showed large variability to repeated identical thermal stimuli. Despite the poor reproducibility of the threshold responses, the distribution of thresholds to thermal ramp stimuli was consistently bimodal, with peaks occurring at 39 and 43°C. The bimodality persisted even when the ipsilateral and contralateral data were pooled. The modes of these threshold distributions conform to the maximum discharge ranges for warm and noxious cutaneous receptors. Thus, it is likely that thermal input to individual PMRF neurones is derived from both types of receptors. The responses of PMRF neurones to repeated thermal stimuli were stable and reproducible with respect to magnitude and time course. The average (static) and maximum (dynamic) responses to thermal stimuli were generally small: for example, the mean of the average responses to ramp stimuli was 5,9 spikes/s ± 11,0 SD, (range -28 to 40 spikes/s), and the mean of the maximum responses was 9,3 spikes/s ± 16,1 SD, (range -46 to 65 spikes/s). The absolute change in firing rate of individual PMRF neurones, and of the population, increased monotonically as a function of the intensity of stepped cutaneous thermal stimuli in the range 40 to 48 °C. However, their resolution, based on their average and maximum responses, was poor. Incorporating the post-stimulus responses into the comparisons between different stimulus intensities marginally increased the resolution of these neurones. Thus, while the majority of PMRF neurones are able to distinguish innocuous from noxious stimuli, few are capable of encoding stimulus intensity within the noxious range (above 43 °C). The majority (70%) of PMRF neurones responded to sustained thermal stimuli with a slow increase or decrease to a new static discharge rate which was maintained with little or no adaptation. Latency to onset of response to stepped thermal stimuli varied from 1 to 50 seconds, and the time to maximal response between 5-60 seconds. Many PMRF neurones also showed marked after-discharge for periods of up to 5 minutes after removal of the stimulus. The thermal receptive fields of over 90% of PMRF neurones were large, incorporating at least both hindlimbs. The extensive receptive field sizes of individual PMRF neurones provides evidence against them having a role in stimulus location. The large number of PMRF neurones showing multimodal convergence, their small magnitude responses, their slow response times, and their large receptive fields strongly suggest that these neurones are not participating in classical sensory discrimination. Rather, they may function as stimulus detectors or alternatively play a role in associative processes.

Background: Binaural hearing improves our ability to understand speech and to localize sounds. Hearing loss can interfere with binaural cues, and despite the success of amplification, ∼25% of people with bilateral hearing loss fit with two hearing aids choose to wear only one (e.g., Brooks and Bulmer, 1981). One explanation is reduced binaural processing, which occurs when the signal presented to one ear interferes with the perception of the signal presented to the other ear (e.g., Jerger et al, 1993). Typical clinical measures, however, are insensitive to binaural processing deficits. Purpose: The purpose of this study was to determine the extent to which behavioral measures of binaural performance were related to electrophysiological measures of binaural processing in subjects with symmetrical pure-tone sensitivity. Research Design: The relationship between middle latency responses (MLRs) and behavioral performance on binaural listening tasks was assessed by Spearman's rho correlation analyses. Separate repeated measures analyses of variance (RMANOVAs) were performed for MLR latency and MLR amplitude. Study Sample: Nineteen subjects were recruited for the present study based on a clinical presentation of symmetrical pure-tone sensitivity with asymmetrical performance on a word-recognition in noise test. This subpopulation of patients included both subjects with and subjects without hearing loss. Data Collection and Analysis: Monaural and binaural auditory processing was measured behaviorally and electrophysiologically in right-handed subjects. The behavioral tests included the Words-in-Noise test (WIN), the dichotic digits test (DDT), and the 500 Hz masking level difference (MLD). Electrophysiologic responses were measured by the binaural interaction component (BIC) of the MLR. The electrophysiological responses were analyzed to examine the effects of peak (Na, Pa, and Nb) and condition (monaural left, monaural right, binaural, and BIC) on MLR amplitude and latency. Results: Significant correlations were found among electrophysiological measures of binaural hearing and behavioral tests of binaural hearing. A strong correlation between the MLD and the binaural Na-Pa amplitude was found (r =.816). Conclusions: The behavioral and electrophysiological measures used in the present study clearly showed evidence of reduced binaural processing in ∼10 of the subjects in the present study who had symmetrical pure-tone sensitivity. These results underscore the importance of understanding binauralauditory processing and how these measures may or may not identify functional auditory problems.

The primary purpose of this investigation was to determine whether temporal coding in the auditory system was the same for younger and older listeners. Temporal coding was assessed by amplitude-modulated auditory steady-state responses (AM ASSRs) as a physiologic measure of phase-locking capability. The secondary purpose of this study was to determine whether AM ASSRs were related to behavioral speech understanding ability. AM ASSRs showed that the ability of the auditory system to phase lock to a temporally altered signal is dependent on modulation rate, carrier frequency, and age of the listener. Specifically, the interaction of frequency and age showed that younger listeners had more phase locking than old listeners at 500 Hz. The number of phase-locked responses for the 500 Hz carrier frequency was significantly correlated to word-recognition performance. In conclusion, the effect of aging on temporal processing, as measured by phase locking with AM ASSRs, was found for low-frequency stimuli where phase locking in the auditory system should be optimal. The exploration, and use, of electrophysiologic responses to measure auditory timing analysis in humans has the potential to facilitate the understanding of speech perception difficulties in older listeners.

No description available.

As animals explore and interact with their surroundings, information about their environment is constantly processed from sensory stimuli into perception. This information informs their behavior, decision-making, and understanding of their world. Information processing and perception have long been thought to be modulated by the behavior state of the animal (Cano et al. 2006; Niell and Stryker 2010; Polack et al. 2013; Poulet & Petersen, 2008; Briggs 2013, Schölvinck et al. 2015). Previous research has shown that behavior state strongly correlates with perceptual performance in a sensory discrimination task in rodents (McGinley et al. 2015, Schriver et al., 2018). However, the neural correlates behind this modulation of perception, information processing, and behavioral performance are not yet fully understood. The first part of this work investigates the relationship between cell-type specific spontaneous cortical activity and behavior state as defined by pupil-linked arousal. Spontaneous activity is essential in understanding the link between behavior state and information processing as it serves as the baseline state of activity prior to processing any stimuli information. Within the sensory cortices, excitatory and inhibitory neurons work in unison to dictate network activity. Three main classes of cortical inhibitory neurons are somatostatin-expressing neurons (SST), vasointestinal peptide-expressing neurons (VIP), and parvalbumin-expressing neurons (PV). These four cell types comprise the VIP disinhibitory circuit, in which VIP neurons disinhibit excitatory neurons by inhibiting PV and SST neurons. PV and SST neurons directly inhibit excitatory cells, so by suppressing their activity VIP neurons indirectly disinhibit excitatory cells. This circuit is a vitally important system used to modify excitatory activity in all cortical regions. The spontaneous activity of excitatory neurons and three classes of inhibitory neurons (somatostatin-expressing neurons (SST), vasointestinal peptide-expressing neurons (VIP), and parvalbumin-expressing neurons (PV)) was individually examined in this study. To visualize in-vivo spontaneous cortical activity, a genetically encoded calcium indicator (GCaMP) was expressed in the somatosensory cortex, and the population-level neural activity was imaged using fiber photometry. Despite the relationship between these neurons as defined by the VIP disinhibitory circuit, the spontaneous activity of excitatory, VIP, PV, and SST neurons was found to positively correlate with pupil size for all of these neuron types. This supports the theory that VIP and other interneuron types may be active in various functions, not just the disinhibition of excitatory cells. Pupil-evoked activity, or spontaneous activity during highly aroused states, was also found to positively correlate with pupil size for all cell types and had the strongest correlation for all correlation types. Therefore, pupil-linked arousal level relates to the increased activity of both excitatory and inhibitory cortical cells. While the first chapter focuses on spontaneous activity, the second focuses on stimulus-evoked activity. Stimulus-evoked activity in the somatosensory pathway can be caused by both internally generated stimuli and external stimuli. In the first step of sensory processing, the sensory receptors cannot distinguish between these two types of stimuli. However, the differentiation between the two is necessary in order to distinguish self from non-self. The motor-related timing signals that influence sensory processing and enable distinction between internally generated and external stimuli is termed corollary discharge. Where and how the mechanism of corollary discharge occurs in the somatosensory system is not well understood. To investigate corollary discharge in the somatosensory system, the neural activity in the somatosensory cortex was analyzed during internally generated stimuli and during delivery of external stimuli. More specifically, the activity in the vibrissa somatosensory cortex of rodents during self-induced whisking and during delivery of an air puff to the whiskers was examined. In the primary and secondary somatosensory cortex, excitatory activity was inhibited just prior to whisking and suppressed to a lower level during whisking in comparison to the activity level during air puff delivery. The three main classes of inhibitory neurons were studied to explore the possibility of local inhibition causing this suppression of the excitatory signal during whisking. VIP, PV and SST neurons all exhibited a similar pre-whisking inhibition and suppression of activity during whisking, eliminating the possibility of their role in pre-whisking inhibition and whisking activity suppression. Other regions involved in the somatosensory pathway and sensorimotor processing, such as the thalamus and motor cortex, were also found to not contribute to pre-whisking inhibition or whisking activity suppression as they were also found to exhibit the same phenomenon. After ruling out cortical inhibitory neurons and somatosensory regions in the involvement of corollary discharge, external higher-order regions were investigated. Previous studies on the sources of corollary discharge in the cerebellum have shown corollary discharge signals originate from coordination of several different higher-order brain regions (Person A., 2019). To determine these potential regions for somatosensory corollary discharge, viral tracing vectors were used to locate regions with long-range inhibitory projections to the somatosensory cortex. The globus pallidus (GP) was first investigated due to its role in voluntary movement and projections to the frontal cortex (Saunders et al. 2015). However, no inhibitory projections from the GP to the somatosensory cortex were found. The striatum, which is mainly GABAergic (and therefore inhibitory), also seemed to be a likely candidate. Preliminary tracing results suggest the striatum does have inhibitory projections to the somatosensory cortex. Further studies of both retrograde and anterograde tracing must be performed to confirm this finding. Nonetheless, the evidence of corollary discharge as seen through pre-whisking inhibition and the suppression of activity during whisking in S1, S2, thalamus, and motor cortex is a novel finding and opens up many avenues for further research.

The work in this thesis is concerned with examining the retinal and cortical contributions to human trichromatic colour vision. Chromatic processing at the cortex level was examined using visual evoked potentials (VEPs). These responses were elicited by chromatic spot stimuli, which were manipulated in order to selectively activate the chromatic processing system. Chromatic processing at the retinal level was examined using the electroretinograms (ERGs) for which cone isolating stimuli were used to assess the nature of L and M cone inputs to cone-opponent mechanisms. The results from the VEP experiments suggest VEP morphology is dependent upon 1) chromatic and or luminance contrast content of the stimulus, 2) stimulus size, and 3) extent to which the chromatic stimulus activates either the L/M or S/(L+M) opponent mechanism. The experiments indicate that chromatic stimulation is indexed by large N1 component and small offset responses. Optimal stimulus size for chromatic isolation is 2-4 ° along L/M axes and 6° along S/(L+M) axis. From the ERG experiments, It has been shown that the low (12Hz) and high (30Hz) temporal frequency flickering stimuli can isolate the chromatic and luminance processing mechanisms in the retina. For low temporal frequency ERGs, the L:M ratio was close to unity and L/M phase difference was close to 180°. For high temporal frequency ERGs, the L:M ratio was more than unity and L/M phase difference was close to 90°. In addition to this, the variation in L:M ratio across the retinal eccentricity was also examined. These results suggest, for the chromatic processing, L:M ratio is close to unity independent of retinal eccentricity and individuals. For the luminance processing, L:M ratio is more than unity and depends upon the region of the retina being stimulated. These findings indicate the maintenance of cone selective input for the chromatic processing across the human retina.

No description available.