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Lead (Pb) causes significant adverse effects on the developing brain, resulting in cognitive and learning disabilities in children. The process by which lead produces these negative changes is largely unknown. The fact that children with these syndromes also show deficits in central auditory processing, however, indicates a speculative but disturbing relationship between lead-exposure, impaired auditory processing, and behavioral dysfunction. Here we studied in rats the changes in cortical spatial tuning impacted by early lead-exposure and their potential restoration to normal by auditory training. We found animals that were exposed to lead early in life displayed significant behavioral impairments compared with naïve controls while conducting the sound-azimuth discrimination task. Lead-exposure also degraded the sound-azimuth selectivity of neurons in the primary auditory cortex. Subsequent sound-azimuth discrimination training, however, restored to nearly normal the lead-degraded cortical azimuth selectivity. This reversal of cortical spatial fidelity was paralleled by changes in cortical expression of certain excitatory and inhibitory neurotransmitter receptor subunits. These results in a rodent model demonstrate the persisting neurotoxic effects of early lead-exposure on behavioral and cortical neuronal processing of spatial information of sound. They also indicate that attention-demanding auditory training may remediate lead-induced cortical neurological deficits even after these deficits have occurred., (© The Author(s) 2018. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.)

Previous studies have suggested that the cellular Ca 2+ and iron homeostasis, which can be regulated by mitochondrial calcium uniporter (MCU), is associated with oxidative stress, apoptosis and many neurological diseases. However, little is known about the role of MCU-mediated Ca 2+ and iron accumulation in traumatic brain injury (TBI). Under physiological conditions, MCU can be inhibited by ruthenium red (RR) and activated by spermine (Sper). In the present study, we used RR and Sper to reveal the role of MCU in mouse and neuron TBI models. Our results suggested that the Ca 2+ and iron concentrations were obviously increased after TBI. In addition, TBI models showed a significant generation of reactive oxygen species (ROS), decrease in adenosine triphosphate (ATP), deformation of mitochondria, up-regulation of deoxyribonucleic acid (DNA) damage and increase in apoptosis. Blockage of MCU by RR prevented Ca 2+ and iron accumulation, abated the level of oxidative stress, improved the energy supply, stabilized mitochondria, reduced DNA damage and decreased apoptosis both in vivo and in vitro. Interestingly, Sper did not increase cellular Ca 2+ and iron concentrations, but suppressed the Ca 2+ and iron accumulation to benefit the mice in vivo. However, Sper had no significant impact on TBI in vitro. Taken together, our data demonstrated for the first time that blockage of MCU-mediated Ca 2+ and iron accumulation was essential for TBI. These findings indicated that MCU could be a novel therapeutic target for treating TBI., (© 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.)

Physiological and behavioral studies in cats show that corticotectal inputs play a critical role in the information-processing capabilities of neurons in the deeper layers of the superior colliculus (SC). Among them, the sensory inputs from functionally related associational cortices are especially critical for SC multisensory integration. However, the underlying mechanism supporting this influence is still unclear. Here, results demonstrate that deactivation of relevant cortices can both dislocate SC visual and auditory spatial receptive fields (RFs) and decrease their overall size, resulting in reduced alignment. Further analysis demonstrated that this RF separation is significantly correlated with the decrement of neurons' multisensory enhancement and is most pronounced in low stimulus intensity conditions. In addition, cortical deactivation could influence the degree of stimulus effectiveness, thereby illustrating the means by which higher order cortices may modify the multisensory activity of SC., (© The Author 2016. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.)

Adult rats were trained to detect the occurrence of a two-element sound sequence in a background of nine other nontarget sound pairs. Training resulted in a modest, enduring, static expansion of the cortical areas of representation of both target stimulus sounds. More importantly, once the initial stimulus A in the target A-B sequence was presented, the cortical "map" changed dynamically, specifically to exaggerate further the representation of the "anticipated" stimulus B. If B occurred, it was represented over a larger cortical area by more strongly excited, more coordinated, and more selectively responding neurons. This biasing peaked at the expected time of B onset with respect to A onset. No dynamic biasing of responses was recorded for any sound presented in a nontarget pair. Responses to nontarget frequencies flanking the representation of B were reduced in area and in response strength only after the presentation of A at the expected time of B onset. This study shows that cortical areas are not representationally static but, to the contrary, can be biased moment by moment in time as a function of behavioral context.

Corticofugal modulation of sub-cortical auditory selectivity has been shown previously in mammals for frequency, amplitude, time, and direction domains in separate studies. As such, these studies do not show if multi-parametric corticofugal modulation can be mediated through the same sub-cortical neuron. Here we specifically studied corticofugal modulation of best frequency (BF), best amplitude (BA), and best azimuth (BAZ) at the same neuron in the inferior colliculus of the big brown bat, Eptesicus fuscus, using focal electrical stimulation in the auditory cortex. Among 53 corticofugally inhibited collicular neurons examined, cortical electrical stimulation produced a shift of all three measurements (i.e., BF, BA, and BAZ) toward the value of stimulated cortical neuron in 13 (24.5%) neurons, two measurements (i.e., BF and BAZ or BA and BAZ) in 19 (36%) neurons, and one measurement in 16 (30%) neurons. Cortical electrical stimulation did not shift any of these measurements in the remaining five (9.5%) neurons. Corticofugally induced collicular BF shift was symmetrical, whereas the shift in collicular BA or BAZ was asymmetrical. The amount of shift in each measurement was significantly correlated with each measurement difference between recorded collicular and stimulated cortical neurons. However, shifts of three measurements were not correlated with each other. Furthermore, average measurement difference between collicular and cortical neurons was larger for collicular neurons with measurement shifts than for those without shifts. These data indicate that multi-parametric corticofugal modulation can be mediated through the same subcortical neuron based on the difference in auditory selectivity between subcortical and cortical neurons.

The spectral, temporal, and intensive selectivity of neurons in the adult primary auditory cortex (A1) is easily degraded in early postnatal life by raising rat pups in the presence of pulsed noise. The nonselective frequency tuning recorded in these rats substantially endures into adulthood. Here we demonstrate that perceptual training applied in these developmentally degraded postcritical-period rats results in the recovery of normal representational fidelity. By using a modified go/no-go training strategy, structured noise-reared rats were trained to identify target auditory stimuli of specific frequency from a set of distractors varying in frequency. Target stimuli changed daily on a random schedule. Consistent with earlier findings, structured noise exposure within the critical period resulted in disrupted tonotopicity within A1 and in degraded frequency-response selectivity for A1 neurons. Tonotopicity and frequency-response selectivity were normalized by perceptual training. Changes induced by training endured without loss for at least 2 months after training cessation. The results further demonstrate the potential utility of perceptual learning as a strategy for normalizing deteriorated auditory representations in older (postcritical-period) children and adults.

The directional selectivity of auditory neurons is one of the essential response properties that underlie sound localization, an important task performed by the mammalian auditory system. Here we evaluated the sound azimuth selectivity of inferior collicular neurons in juvenile bats, Myotis chinensis, at the age of 15 days under free-field stimulation conditions. Compared with those in adult bats, neurons in juvenile bats were broadly tuned to sound azimuth angles as indicated by both the type and width of the azimuth selectivity curves. Their best azimuth was distributed over a wide range and, moreover, the adult-like relationship between the best azimuth and the best frequency of these neurons was not developed. These data indicate that the directional selectivity of inferior collicular neurons, like other response properties examined previously, undergoes considerable change during postnatal maturation.

In our previous study, we have shown that the recovery cycle of most neurons in the inferior colliculus (IC) of the big brown bat, Eptesicus fuscus, is typically longer at ipsilateral azimuth than at contralateral azimuth under free-field stimulation conditions. The present study is to test the hypothesis that this azimuth-dependent recovery cycle may contribute to the variation of directional selectivity of IC neurons with sequential presented sound pulses within a pulse train. A 300-ms pulse train containing nine sound pulses of 4-ms with an inter-pulse interval of 33.3 ms was delivered at several selected azimuthal angles between +/-80 degrees lateral in the frontal auditory space of a bat. A family of nine directional selectivity curves was plotted with a neuron's number of impulses in response to each individual pulse against the azimuthal angles. The type and sharpness of these directional selectivity curves were then compared in relation to pulse position within the pulse train. All 675 directional selectivity curves obtained from 75 IC neurons could be described as directionally selective (423, 63%), hemifield (220, 32%), or non-directional (32, 5%). The directional selectivity curves of 45 (60%) neurons did not vary with pulse position. However, those of the remaining neurons (30, 40%) changed from one type to another such that the number of neurons with directionally selective curves progressively increased and the number of neurons with hemifield and non-directional selectivity curves decreased with increasing pulse position within the pulse train. Among 68 IC neurons whose directional selectivity curves were compared quantitatively, directional selectivity determined with sequentially presented sound pulses significantly increased in 38 (56%) neurons; decreased in 18 (26%) neurons but did not change in 12 (18%) neurons. This change of directional selectivity was due to the variation in recovery cycle of these IC neurons with azimuthal angle as we hypothesized.

The recovery cycle of auditory neurons is an important neuronal property, which determines a neuron's ability to respond to pairs of sounds presented at short inter-sound intervals. This property is particularly important for bats, which rely upon analysis of returning echoes to extract the information about targets after emission of intense orientation sounds. Because target direction often changes throughout the course of hunting, the changing echo direction may affect the recovery cycle and thus temporal processing of auditory neurons. In this study, we examined the effect of sound azimuth on the recovery cycle of inferior collicular (IC) neurons in the big brown bat, Eptesicus fuscus, under free-field stimulation conditions. Our study showed that the recovery cycle of most IC neurons (42/49, 86%) was longer when determined with sounds delivered at 40 degrees ipsilateral (i40 degrees ) than at 40 degrees contralateral (c40 degrees ) to the recording site. To study the contribution of GABAergic inhibition to sound azimuth-dependent recovery cycle, we compared the recovery cycle of IC neurons determined at two sound azimuths before and during iontophoretic application of bicuculline, an antagonist for GABA(A) receptors. Bicuculline application produced a greater decrease of the recovery cycle of these neurons at i40 degrees than at c40 degrees. As a result, the azimuth-dependent recovery cycle of these neurons was abolished or greatly reduced. Possible mechanisms underlying these observations and biological relevance to bat echolocation are discussed.

Key points: It has been known for some time that sensory information of one type can bias the spatial perception of another modality. However, there is a lack of evidence of this occurring in individual neurons.In the present study, we found that the spatial receptive field of superior colliculus multisensory neurons could be dynamically shifted by a preceding stimulus in a different modality.The extent to which the receptive field shifted was dependent on both temporal and spatial gaps between the preceding and following stimuli, as well as the salience of the preceding stimulus.This result provides a neural mechanism that could underlie the process of cross‐modal spatial calibration. Psychophysical studies have shown that the different senses can be spatially entrained by each other. This can be observed in certain phenomena, such as ventriloquism, in which a visual stimulus can attract the perceived location of a spatially discordant sound. However, the neural mechanism underlying this cross‐modal spatial recalibration has remained unclear, as has whether it takes place dynamically. We explored these issues in multisensory neurons of the cat superior colliculus (SC), a midbrain structure that involves both cross‐modal and sensorimotor integration. Sequential cross‐modal stimulation showed that the preceding stimulus can shift the receptive field (RF) of the lagging response. This cross‐modal spatial calibration took place in both auditory and visual RFs, although auditory RFs shifted slightly more. By contrast, if a preceding stimulus was from the same modality, it failed to induce a similarly substantial RF shift. The extent of the RF shift was dependent on both temporal and spatial gaps between the preceding and following stimuli, as well as the salience of the preceding stimulus. A narrow time gap and high stimulus salience were able to induce larger RF shifts. In addition, when both visual and auditory stimuli were presented simultaneously, a substantial RF shift toward the location‐fixed stimulus was also induced. These results, taken together, reveal an online cross‐modal process and reflect the details of the organization of SC inter‐sensory spatial calibration. Key points: It has been known for some time that sensory information of one type can bias the spatial perception of another modality. However, there is a lack of evidence of this occurring in individual neurons.In the present study, we found that the spatial receptive field of superior colliculus multisensory neurons could be dynamically shifted by a preceding stimulus in a different modality.The extent to which the receptive field shifted was dependent on both temporal and spatial gaps between the preceding and following stimuli, as well as the salience of the preceding stimulus.This result provides a neural mechanism that could underlie the process of cross‐modal spatial calibration. [ABSTRACT FROM AUTHOR]

Abstract: In our recent study of corticofugal modulation of collicular amplitude sensitivity of the big brown bat, Eptesicus fuscus, we suggested that the corticofugal modulation is based upon the best frequency (BF) differences and the relative amplitude sensitivity difference between collicular (IC) and cortical (AC) neurons but not the absolute amplitude sensitivity of IC and AC neurons. To show that corticofugal modulation is systematic and multiparametric, we studied corticofugal modulation of directional sensitivity in 89 corticofugally inhibited IC neurons in the same bat species under free field stimulation conditions. A neuron’s directional sensitivity was expressed with the azimuthal range (AR) at 50% below the maximum of each directional sensitivity curve and the best azimuth (BAZ) at which the neuron discharged maximally. Cortical electrical stimulation did not affect the directional sensitivity of 40 (45%) neurons with BFIC–AC differences of 7.3±4.4kHz but sharpened the directional sensitivity of other 49 (55%) neurons with BFIC–AC differences of 2.3±1.8kHz. Corticofugal modulation sharpened directional sensitivity curves of IC neurons by decreasing the AR and shifting collicular BAZ toward cortical BAZ. The decrease in AR and the shift in BAZ increased significantly with ARIC–AC and BAZIC–AC differences but not with absolute AR and BAZ of IC and AC neurons or BFIC–AC differences. Corticofual modulation also shifted collicular BF toward cortical BF. The shift in BF increased significantly with BFIC–AC differences but not with the BF of IC and AC neurons or BAZ shift. Consonant with our previous study, these data indicate that corticofugal modulation of collicular directional sensitivity is based on topographic projections between the IC and the AC and the difference in directional sensitivity but not the absolute directional sensitivity of IC or AC neurons. [Copyright &y& Elsevier]

Recent studies have shown that the corticofugal system systematically modulates and improves subcortical signal processing in the frequency, time and spatial domains. The present study examined corticofugal modulation of amplitude sensitivity of 113 corticofugally inhibited neurons in the central nucleus of the inferior colliculus (IC) of the big brown bat, Eptesicus fuscus. Cortical electrical stimulation decreased the number of impulses and increased the response latency of these neurons. They had an average of 5.9±4.4 kHz best frequency (BF) differences between collicular and electrically stimulated cortical neurons. Cortical electrical stimulation synchronized with sound stimulation for 30 min compressed the rate–amplitude functions of half (56, 49.6%) of these collicular neurons and shifted their minimum thresholds (MT) and dynamic ranges (DR) toward that of electrically stimulated cortical neurons for as long as 40 min. These collicular neurons had an average of 1.6±1.4 kHz BF differences. The shift in collicular MT and DR significantly increased with differences in MT and DR between collicular and cortical neurons. Cortical electrical stimulation also shifted the BF and best amplitude (BA) of collicular neurons toward that of cortical neurons. The BF shift increased with BF differences and the BA shift increased with BA differences. These data suggest that the corticofugal system modulates collicular responses on the basis of topographic projections between the IC and auditory cortex. However, corticofugal modulation of collicular amplitude sensitivity is primarily dependent upon the difference but not the absolute amplitude sensitivity between collicular and cortical neurons. [Copyright &y& Elsevier]

This study examined the effect of temporally patterned pulse trains on intensity and frequency sensitivity of inferior collicular neurons of the big brown bat, Eptesicus fuscus. Intensity sensitivity of inferior collicular neurons was expressed by the dynamic range and slope of rate-intensity functions. Inferior collicular neurons with non-monotonic rate-intensity functions have smaller dynamic ranges and larger slopes than neurons with monotonic or saturated rate-intensity functions. Intensity sensitivity of all inferior collicular neurons improved by increasing the number of non-monotonic rate-intensity functions when the pulse repetition rate of pulse trains increased from 10 to 30 pulses per second. Intensity sensitivity of 43% inferior collicular neurons further improved when the pulse repetition rate of pulse trains increased still from 30 to 90 pulses per second. Frequency sensitivity of inferior collicular neurons was expressed by the Q10, Q20, and Q30 values of threshold frequency tuning curves and bandwidths of isointensity frequency tuning curves. Threshold frequency tuning curves of all inferior collicular neurons were V-shape and mirror-images of their counterpart isointensity frequency tuning curves. The Q10, Q20, and Q30 values of threshold frequency tuning curves of all inferior collicular neurons progressively increased and bandwidths of isointensity frequency tuning curves decreased with increasing pulse repetition rate in temporally patterned pulse trains. Biological relevance of these findings to bat echolocation is discussed. [ABSTRACT FROM AUTHOR]

Previous studies have shown that inferior collicular neurons of the big brown bat, Eptesicus fuscus, serve as short-, band-, long- and all-pass filters for sound durations. Neurons with band-, short- and long-pass filtering characteristics discharged maximally to a specific sound duration or a range of sound durations. In contrast, neurons with all-pass filtering characteristics do not have duration selectivity. To determine if duration-tuning characteristics of collicular neurons were tolerant to changes in sound intensity, we examined the duration-tuning characteristics of collicular neurons using a wide range of sound intensities. Duration-tuning characteristics examined included the type, bandwidth and slope of duration-tuning curves. Sound intensity delivered within 20 dB of minimum threshold did not affect duration-tuning characteristics of all collicular neurons studied. Sound intensities at still higher levels did not affect the tuning characteristics of two-thirds of collicular neurons but decreased the duration selectivity and changed the duration-tuning curves of the remaining one-third of neurons from one type to another. However, these two groups of duration-tuning collicular neurons were not separately organized inside the inferior colliculus. The biological relevance of these findings to bat echolocation is discussed. [ABSTRACT FROM AUTHOR]

Enduring deficits in temporal processing can be induced in the auditory cortex by rearing infant rats in the presence of low frequency–modulated noises. We found that it was possible to restore normal temporal processing, overcoming deficits induced during the critical period, by intensively training developmentally impaired animals as juveniles or young adults. Re-normalized cortical temporal response characteristics were sustained long after training cessation. [ABSTRACT FROM AUTHOR]

This study examined the effect of bicuculline application on sharpness of frequency tuning curves (FTCs) of bat inferior collicular neurons plotted under three different pulse repetition rates (PRRs) of 10, 30 and 90 pulses per second. The sharpness of FTCs of collicular neurons, which was expressed in Qn (Q10, Q20, Q30) and bandwidths (90, 75 and 50% of the maximal response at the best frequency), improved with increasing PRR. However, this PRR-dependent frequency selectivity of collicular neurons was abolished during bicuculline application. This observation suggests that GABAergic inhibition contributes more effectively to sharpening of FTCs at higher than at lower PRRs. [Copyright &y& Elsevier]