Academic literature on the topic 'Neural processing latencies'

The Poisson variability in cortical neural responses has been typically modeled using spike averaging techniques, such as trial averaging and rate coding, since such methods can produce reliable correlates of behavior. However, mechanisms that rely on counting spikes could be slow and inefficient and thus might not be useful in the brain for computations at timescales in the 10 millisecond range. This issue has motivated a search for alternative spike codes that take advantage of spike timing and has resulted in many studies that use synchronized neural networks for communication. Here we focus on recent studies that suggest that the gamma frequency may provide a reference that allows local spike phase representations that could result in much faster information transmission. We have developed a unified model (gamma spike multiplexing) that takes advantage of a single cycle of a cell's somatic gamma frequency to modulate the generation of its action potentials. An important consequence of this coding mechanism is that it allows multiple independent neural processes to run in parallel, thereby greatly increasing the processing capability of the cortex. System-level simulations and preliminary analysis of mouse cortical cell data are presented as support for the proposed theoretical model.

Variability in perception between individuals may be a consequence of different inherent neural processing speeds. To assess whether alpha oscillations systematically reflect a feedback pacing mechanism for cortical processing during visual perception, comparisons were made between alpha oscillations, visual suppression from TMS, visual evoked responses, and metacontrast masking. Peak alpha oscillation frequencies, measured through scalp EEG recordings, significantly correlated with the optimum latencies for visual suppression from TMS of early visual cortex. Individuals with shorter alpha periods (i.e., higher peak alpha frequencies) processed visual information faster than those with longer alpha periods (i.e., lower peak alpha frequencies). Moreover, peak alpha oscillation periods and optimum TMS visual suppression latencies predicted the latencies of late but not early visual evoked responses. Together, these findings demonstrate an important role of alpha oscillatory and late feedback activity in visual cortex for conscious perception. They also show that the timing for visual awareness varies across individuals, depending on the pace of one's endogenous oscillatory cycling frequency.

Herein, we investigated the effects of passive heat stress on human somatosensory processing recorded by somatosensory-evoked potentials (SEPs). Fifteen healthy subjects received a median nerve stimulation at the left wrist under two thermal conditions: Heat Stress and normothermic Time Control. The latencies and amplitudes of P14, N20, P25, N35, P45, and N60 at C4′ and P14, N18, P22, and N30 at Fz were evaluated. Under the Heat Stress condition, SEPs were recorded at normothermic baseline (1st), early in heat stress (2nd), when esophageal temperature had increased by ∼1.0°C (3rd) and ∼2.0°C (4th), and after heat stress (5th). In the Time Control condition, SEPs were measured at the same time intervals as those in the Heat Stress condition. The peak latencies and amplitudes of SEPs did not change early in heat stress. However, the latencies of P14, N20, and N60 at C4′ and P14, N18, and P22 at Fz were significantly shorter in the 4th session than in the 1st session. Furthermore, the peak amplitudes of P25 and N60 at C4′, and P22 and N30 at Fz decreased with increases in body temperature. On the other hand, under the Time Control condition, no significant differences were observed in the amplitudes or latencies of any component of SEPs. These results suggested that the conduction velocity of the ascending somatosensory input was accelerated by increases in body temperature, and hyperthermia impaired the neural activity of cortical somatosensory processing.

The goal of this study was to test the hypothesis that neural processes for language are heterogeneous in their adaptations to maturation and experience. This study examined whether the neural processes for open-and closed-class words are differentially affected by delays in second-language immersion. In English, open-class words primarily convey referential meaning, whereas closed-class words are primarily related to grammatical information in sentence processing. Previous studies indicate that event-related brain potentials (ERPs) elicited by these word classes display nonidentical distributions and latencies, show different developmental time courses, and are differentially affected by early language experience in Deaf individuals. In this study, ERPs were recorded from 10 monolingual English speakers and 53 Chinese-English bilingual speakers who were grouped according to their age of immersion in English: 1–3, 4–6, 7–10, 11–13, and >15 years of age. Closed-class words elicited an N280 that was largest over left anterior electrode sites for all groups. However, the peak latency was later (>35 ms) in bilingual speakers immersed in English after 7 years of age. In contrast, the latencies and distributions of the N350 elicited by open-class words were similar in all groups. In addition, the N400, elicited by semantic anomalies (open-class words that violated semantic expectation), displayed increased peak latencies for only the later-learning bilingual speakers (>11 years). These results are consistent with the hypothesis that language subprocesses are differentially sensitive to the timing of second-language experience.

AbstractObjective:Poor auditory speech perception in geriatrics is attributable to neural de-synchronisation due to structural and degenerative changes of ageing auditory pathways. The speech-evoked auditory brainstem response may be useful for detecting alterations that cause loss of speech discrimination. Therefore, this study aimed to compare the speech-evoked auditory brainstem response in adult and geriatric populations with normal hearing.Methods:The auditory brainstem responses to click sounds and to a 40 ms speech sound (the Hindi phoneme |da|) were compared in 25 young adults and 25 geriatric people with normal hearing. The latencies and amplitudes of transient peaks representing neural responses to the onset, offset and sustained portions of the speech stimulus in quiet and noisy conditions were recorded.Results:The older group had significantly smaller amplitudes and longer latencies for the onset and offset responses to |da| in noisy conditions. Stimulus-to-response times were longer and the spectral amplitude of the sustained portion of the stimulus was reduced. The overall stimulus level caused significant shifts in latency across the entire speech-evoked auditory brainstem response in the older group.Conclusion:The reduction in neural speech processing in older adults suggests diminished subcortical responsiveness to acoustically dynamic spectral cues. However, further investigations are needed to encode temporal cues at the brainstem level and determine their relationship to speech perception for developing a routine tool for clinical decision-making.

Objectives. Cochlear implant (CI) users typically report impaired ability to understand speech in noise. Speech understanding in CI users decreases with noise due to reduced temporal processing ability, and speech perceptual errors involve stop consonants distinguished by voice onset time (VOT). The current study examined the effects of noise on various speech perception tests while at the same time used cortical auditory evoked potentials (CAEPs) to quantify the change of neural processing of speech sounds caused by noise. We hypothesized that the noise effects on VOT processing can be reflected in N1/P2 measures, the neural changes relate to behavioral speech perception performances.Methods. Ten adult CI users and 15 normal-hearing (NH) people participated in this study. CAEPs were recorded from 64 scalp electrodes in both quiet and noise (signal-to-noise ratio +5 dB) and in passive and active (requiring consonant discrimination) listening. Speech stimulus was synthesized consonant-vowels with VOTs of 0 and 50 ms. N1-P2 amplitudes and latencies were analyzed as a function of listening condition. For the active condition, the P3b also was analyzed. Behavioral measures included a variety of speech perception tasks.Results. For good performing CI users, performance in most speech test was lower in the presence of noise masking. N1 and P2 latencies became prolonged with noise masking. The P3b amplitudes were smaller in CI groups compared to NH. The degree of P2 latency change (0 vs. 50 ms VOT) was correlated with consonant perception in noise.Conclusion. The effects of noise masking on temporal processing can be reflected in cortical responses in CI users. N1/P2 latencies were more sensitive to noise masking than amplitude measures. Additionally, P2 responses appear to have a better relationship to speech perception in CI users compared to N1.

We herein investigated the effects of face/head and whole body cooling during passive heat stress on human somatosensory processing recorded by somatosensory-evoked potentials (SEPs) at C4′ and Fz electrodes. Fourteen healthy subjects received a median nerve stimulation at the left wrist. SEPs were recorded at normothermic baseline (Rest), when esophageal temperature had increased by ~1.2°C (heat stress: HS) during passive heating, face/head cooling during passive heating (face/head cooling: FHC), and after HS (whole body cooling: WBC). The latencies and amplitudes of P14, N20, P25, N35, P45, and N60 at C4′ and P14, N18, P22, and N30 at Fz were evaluated. Latency indicated speed of the subcortical and cortical somatosensory processing, while amplitude reflected the strength of neural activity. Blood flow in the internal and common carotid arteries (ICA and CCA, respectively) and psychological comfort were recorded in each session. Increases in esophageal temperature due to HS significantly decreased the amplitude of N60, psychological comfort, and ICA blood flow in the HS session, and also shortened the latencies of SEPs (all, P < 0.05). While esophageal temperature remained elevated, FHC recovered the peak amplitude of N60, psychological comfort, and ICA blood flow toward preheat baseline levels as well as WBC. However, the latencies of SEPs did not recover in the FHC and WBC sessions. These results suggest that impaired neural activity in cortical somatosensory processing during passive HS was recovered by FHC, whereas conduction velocity in the ascending somatosensory input was accelerated by increases in body temperature.

Objective. The goal of this study was to begin to explore whether the beneficial auditory neural effects of early music training persist throughout life and influence age-related changes in neurophysiological processing of sound.Design. Cortical auditory evoked potentials (CAEPs) elicited by harmonic tone complexes were examined, including P1-N1-P2, mismatch negativity (MMN), and P3a.Study Sample. Data from older adult musicians (n=8) and nonmusicians (n=8) (ages 55–70 years) were compared to previous data from young adult musicians (n=40) and nonmusicians (n=20) (ages 18–33 years).Results. P1-N1-P2 amplitudes and latencies did not differ between older adult musicians and nonmusicians; however, MMN and P3a latencies for harmonic tone deviances were earlier for older musicians than older nonmusicians. Comparisons of P1-N1-P2, MMN, and P3a components between older and young adult musicians and nonmusicians suggest that P1 and P2 latencies are significantly affected by age, but not musicianship, while MMN and P3a appear to be more sensitive to effects of musicianship than aging.Conclusions. Findings support beneficial influences of musicianship on central auditory function and suggest a positive interaction between aging and musicianship on the auditory neural system.

The present study aimed to investigate the effects of aerobic exercise on human somatosensory processing recorded by somatosensory evoked potentials (SEPs) under temperate [TEMP, 20°C and 40% relative humidity (RH)] and hot (HOT, 35°C and 30% RH) environments. Fifteen healthy subjects performed 4 × 15-min bouts of a moderate cycling exercise [mean power output: 156.5 ± 7.7 (SE) W], with a 10-min rest period and received a posterior tibial nerve stimulation at the left ankle before and after each exercise bout; SEPs were recorded in five sessions; 1st (pre), 2nd (post-1st exercise bout), 3rd (post-2nd exercise bout), 4th (post-3rd exercise bout), and 5th (post-4th exercise bout). The peak latencies and amplitudes of the P37, N50, P60, and N70 components at Cz were evaluated. The latencies of P37, N50, P60, and N70 were significantly shorter with the repetition of aerobic exercise, and these shortened latencies were significantly greater in the HOT condition than in the TEMP condition (P37: 3rd, P < 0.05, and 5th, P < 0.01; P60: 4th, P < 0.05, and 5th, P < 0.01; N70: 4th, P < 0.05, and 5th, P < 0.001). No significant differences were observed in the amplitudes of any SEP component under either thermal condition. These results suggest that the conduction velocity of the ascending somatosensory input was accelerated by increases in body temperature, and aerobic exercise did not alter the strength of neural activity in cortical somatosensory processing.

The respective roles of ventral and dorsal cortical processing streams are still under discussion in both vision and audition. We characterized neural responses in the caudal auditory belt cortex, an early dorsal stream region of the macaque. We found fast neural responses with elevated temporal precision as well as neurons selective to sound location. These populations were partly segregated: Neurons in a caudomedial area more precisely followed temporal stimulus structure but were less selective to spatial location. Response latencies in this area were even shorter than in primary auditory cortex. Neurons in a caudolateral area showed higher selectivity for sound source azimuth and elevation, but responses were slower and matching to temporal sound structure was poorer. In contrast to the primary area and other regions studied previously, latencies in the caudal belt neurons were not negatively correlated with best frequency. Our results suggest that two functional substreams may exist within the auditory dorsal stream.

There has been considerable debate about how visual information is processed for the perception of stimuli and the generation of motor responses to the same stimuli. While there are well-documented differences in conduction latencies of the luminance and chromatic pathways, it is unclear if information that is integrated from these pathways is used in a similar way across motor and perceptual tasks. Key aspects of human behaviour have different requirements in terms of the spatial and temporal resolution required to complete the task. Certain tasks may therefore rely on processing of information that has spatial or temporal characteristics that are most informative for that specific task. Three studies examined tasks with different task demands; a simple reaction time task, three perceptual asynchrony tasks and a reaching task. Differences in processing for perceptual and motor responses were investigated by measuring differences in the relative response latencies to chromatic and luminance stimuli in these tasks. In the first study, I investigated ways to equate the contrast of different chromatic and luminance stimuli. I then measured RTs to these stimuli as a function of contrast. RTs to luminance stimuli were approximately 45 and 60 ms shorter than RTs to L-M and S-cone stimuli respectively. RTs decreased as a function of contrast more rapidly to luminance stimuli than to chromatic stimuli. In the second study, I used three tasks to investigate relative latencies with which chromatic and luminance stimuli were perceived to appear. I demonstrated that two of the existing tasks typically used to investigate perceptual asynchrony were unsuited for this comparison. I then developed a task that determined the minimum backmask onset delays that allowed participants to accurately locate stimuli. The differences in the delays between the pathways indicated the differences in the latencies in when the stimuli appeared to participants. The temporal advantage for the luminance pathway was only approximately 9 and 14 ms over the L-M and S-cone pathways respectively. In the final study, I examined the delays in correcting rapid reaches to luminance and chromatic stimuli. The temporal advantage for the luminance pathway was approximately 15 and 20 ms over the L-M and S-cone pathways respectively. The temporal advantage found for the luminance pathway in the RT task may be larger than the advantage that would be predicted on the basis of differences in conduction latencies alone. Thus, the relatively rapid decrease in RT with contrast for the luminance pathway, and the large dissociation in the response latencies measured in the RT and perceptual tasks, is consistent with there being separate decision making processes for RT and perception, with the RT response being relatively more reliant on luminance information. The reaching correction response however appears to rely on a similar contribution from the pathways to the perception of the stimuli. It is discussed how these stimuli and results could be readily utilised to extend these comparisons to further develop understanding of commonality and differences in processing visual information for different visual tasks.
Thesis (Ph.D.) (Research by Publication) -- University of Adelaide, School of Psychology, 2014.

Auditory Brainstem Responses (ABR) are short-latency electric potentials from the auditory nervous system that can be evoked by presenting transient acoustic stimuli to the ear. Sources of the ABR are the auditory nerve and brainstem auditory nuclei. Clinical application of ABRs includes identification of the site of lesion in retrocochlear hearing loss, establishing functional integrity of the auditory nerve, and objective audiometry. Recording of ABR requires a measurement setup with a high-quality amplifier with adequate filtering and low skin-electrode impedance to reduce non-physiological interference. Furthermore, signal averaging and artifact rejection are essential tools for obtaining a good signal-to-noise ratio. Comparing latencies for different peaks at different stimulus intensities allows the determination of hearing threshold, location of the site of lesion, and establishment of neural integrity. Audiological assessment of infants who are referred after failing hearing screening relies on accurate estimation of hearing thresholds. Frequency-specific ABR using tone-burst stimuli is a clinically feasible method for this. Appropriate correction factors should be applied to estimate the hearing threshold from the ABR threshold. Whenever possible, obtained thresholds should be confirmed with behavioral testing. The Binaural Interaction Component of the ABR provides important information regarding binaural processing in the brainstem.