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The ability to spontaneously feel a beat in music is a phenomenon widely believed to be unique to humans. Though beat perception involves the coordinated engagement of sensory, motor and cognitive processes in humans, the contribution of low-level auditory processing to the activation of these networks in a beat-specific manner is poorly understood. Here, we present evidence from a rodent model that midbrain preprocessing of sounds may already be shaping where the beat is ultimately felt. For the tested set of musical rhythms, on-beat sounds on average evoked higher firing rates than off-beat sounds, and this difference was a defining feature of the set of beat interpretations most commonly perceived by human listeners over others. Basic firing rate adaptation provided a sufficient explanation for these results. Our findings suggest that midbrain adaptation, by encoding the temporal context of sounds, creates points of neural emphasis that may influence the perceptual emergence of a beat.
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Percepción Auditiva/fisiología , Gerbillinae/fisiología , Colículos Inferiores/fisiología , Música , Desempeño Psicomotor , Estimulación Acústica , Adulto , Animales , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto JovenRESUMEN
A 2.5 Gb/s differential binary phase-shift keying (DPSK) transmitter based on direct phase modulation of a vertical cavity surface emitting lasers (VCSEL) using its own chirp is proposed. The VCSEL, which has a wavelength of 1539.84 nm, has been characterized both statically and dynamically. The sensitivity of a single photodiode heterodyne receiver using the proposed 2.5 Gb/s VCSEL transmitter is -39.5 dBm. Thus, this transmitter is an extremely cost-effective solution for future access networks.
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Signal and noise correlations, a prominent feature of cortical activity, reflect the structure and function of networks during sensory processing. However, in addition to reflecting network properties, correlations are also shaped by intrinsic neuronal mechanisms. Here we show that spike threshold transforms correlations by creating nonlinear interactions between signal and noise inputs; even when input noise correlation is constant, spiking noise correlation varies with both the strength and correlation of signal inputs. We characterize these effects systematically in vitro in mice and demonstrate their impact on sensory processing in vivo in gerbils. We also find that the effects of nonlinear correlation transfer on cortical responses are stronger in the synchronized state than in the desynchronized state, and show that they can be reproduced and understood in a model with a simple threshold nonlinearity. Since these effects arise from an intrinsic neuronal property, they are likely to be present across sensory systems and, thus, our results are a critical step toward a general understanding of how correlated spiking relates to the structure and function of cortical networks.
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Potenciales de Acción/fisiología , Corteza Cerebral/fisiología , Red Nerviosa/fisiología , Ruido , Dinámicas no Lineales , Estimulación Acústica/métodos , Animales , Gerbillinae , Masculino , Ratones , Ratones Endogámicos C57BLRESUMEN
1 Gbps full-duplex optical links for 6.25 GHz ultra dense WDM frequency slots are demonstrated and optimized for cost-effective metro-access networks. The OLT-ONU downlinks are based on 1 Gbps Nyquist-DPSK using MZM and single-detector heterodyne reception obtaining a sensitivity of -52 dBm. The ONU-OLT uplinks are based on 1 Gbps NRZ-DPSK by directly phase modulated DFB and also single-detector heterodyne reception obtaining same sensitivity of -52 dBm. The power budget of full-duplex link is 43 dB. These proposed links can provide service to 16 (32) users at each 100 (200) GHz WDM channel.
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To understand the strategies used by the brain to analyze complex environments, we must first characterize how the features of sensory stimuli are encoded in the spiking of neuronal populations. Characterizing a population code requires identifying the temporal precision of spiking and the extent to which spiking is correlated, both between cells and over time. In this study, we characterize the population code for speech in the gerbil inferior colliculus (IC), the hub of the auditory system where inputs from parallel brainstem pathways are integrated for transmission to the cortex. We find that IC spike trains can carry information about speech with sub-millisecond precision, and, consequently, that the temporal correlations imposed by refractoriness can play a significant role in shaping spike patterns. We also find that, in contrast to most other brain areas, the noise correlations between IC cells are extremely weak, indicating that spiking in the population is conditionally independent. These results demonstrate that the problem of understanding the population coding of speech can be reduced to the problem of understanding the stimulus-driven spiking of individual cells, suggesting that a comprehensive model of the subcortical processing of speech may be attainable in the near future.
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Percepción del Habla/fisiología , Estimulación Acústica , Algoritmos , Animales , Corteza Auditiva/fisiología , Vías Auditivas/fisiología , Tronco Encefálico/fisiología , Fenómenos Electrofisiológicos/fisiología , Gerbillinae , Colículos Inferiores/fisiología , Modelos Lineales , Masculino , Modelos Neurológicos , Periodo Refractario Electrofisiológico/fisiologíaRESUMEN
Cisplatin is an anticancer agent marred by nephrotoxicity; however, limiting this adverse effect may allow the use of higher doses to improve its efficacy. Cilastatin, a small molecule inhibitor of renal dehydropeptidase I, prevents proximal tubular cells from undergoing cisplatin-induced apoptosis in vitro. Here, we explored the in vivo relevance of these findings and the specificity of protection for kidney cells in cisplatin-treated rats. Cisplatin increased serum blood urea nitrogen and creatinine levels, and the fractional excretion of sodium. Cisplatin decreased the glomerular filtration rate, promoted histological renal injury and the expression of many pro-apoptotic proteins in the renal cortex, increased the Bax/Bcl2 ratio, and oxidative stress in kidney tissue and urine. All these features were decreased by cilastatin, which preserved renal function but did not modify the pharmacokinetics of cisplatin area under the curve. The cisplatin-induced death of cervical, colon, breast, and bladder-derived cancer cell lines was not prevented by cilastatin. Thus, cilastatin has the potential to prevent cisplatin nephrotoxicity without compromising its anticancer efficacy.
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Antineoplásicos , Apoptosis/efectos de los fármacos , Cilastatina/farmacología , Cisplatino , Enfermedades Renales/prevención & control , Riñón/efectos de los fármacos , Inhibidores de Proteasas/farmacología , Animales , Antineoplásicos/farmacocinética , Proteínas Reguladoras de la Apoptosis/metabolismo , Área Bajo la Curva , Biomarcadores/sangre , Nitrógeno de la Urea Sanguínea , Peso Corporal/efectos de los fármacos , Línea Celular Tumoral , Cisplatino/farmacocinética , Cisplatino/toxicidad , Creatinina/sangre , Citoprotección , Dipeptidasas/antagonistas & inhibidores , Dipeptidasas/metabolismo , Modelos Animales de Enfermedad , Relación Dosis-Respuesta a Droga , Proteínas Ligadas a GPI/antagonistas & inhibidores , Proteínas Ligadas a GPI/metabolismo , Tasa de Filtración Glomerular/efectos de los fármacos , Riñón/enzimología , Riñón/patología , Riñón/fisiopatología , Enfermedades Renales/sangre , Enfermedades Renales/inducido químicamente , Enfermedades Renales/enzimología , Enfermedades Renales/patología , Enfermedades Renales/fisiopatología , Masculino , Natriuresis/efectos de los fármacos , Estrés Oxidativo/efectos de los fármacos , Ratas , Ratas Wistar , PorcinosRESUMEN
A 20 Gb/s quaternary TDM-PAM passive optical network with chirped and non-linear optical transmitters is experimentally demonstrated. The migration from legacy TDM-PONs and the implications of using available 10 Gb/s components are analyzed. We show that a loss budget of 27.3 dB is compatible together with a packet power ratio of 10 dB between loud and soft optical network units.
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As multi-electrode and imaging technology begin to provide us with simultaneous recordings of large neuronal populations, new methods for modelling such data must also be developed. We present a model of responses to repeated trials of a sensory stimulus based on thresholded Gaussian processes that allows for analysis and modelling of variability and covariability of population spike trains across multiple time scales. The model framework can be used to specify the values of many different variability measures including spike timing precision across trials, coefficient of variation of the interspike interval distribution, and Fano factor of spike counts for individual neurons, as well as signal and noise correlations and correlations of spike counts across multiple neurons. Using both simulated data and data from different stages of the mammalian auditory pathway, we demonstrate the range of possible independent manipulations of different variability measures, and explore how this range depends on the sensory stimulus. The model provides a powerful framework for the study of experimental and surrogate data and for analyzing dependencies between different statistical properties of neuronal populations.
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Redes Neurales de la Computación , Algoritmos , Animales , Vías Auditivas/anatomía & histología , Simulación por Computador , Interpretación Estadística de Datos , Potenciales Postsinápticos Excitadores/fisiología , Humanos , Procesamiento de Imagen Asistido por Computador/métodos , Modelos Neurológicos , Modelos Estadísticos , Neuroimagen/estadística & datos numéricos , Neuronas/fisiología , Distribución Normal , Relación Señal-Ruido , Factores de TiempoRESUMEN
BACKGROUND: There are few clinical data on retinal involvement after acute exposure to high concentrations mercury and the available reports are based on a small number of patients suffering chronic exposure. The purpose of this paper is to report findings in workers acutely exposed to very high concentrations of mercury vapor with the aim of providing data on a possible direct retinal involvement. METHODS: Twenty-nine patients and 16 controls were evaluated in a comparative case series. Mercury levels in blood and urine samples, visual acuity (VA), contrast sensitivity (CS), visual field (VF), color discrimination and optical coherence tomography (OCT) were recorded. The pattern reversal visual-evoked potentials (PRVEP), full-field and multifocal electroretinography (ffERG/mfERG), pattern electroretinography (PERG), systemic symptoms, presence of erethism, and electromyography (EMG) were also gathered. A descriptive analysis was performed. The correlations between variables also were studied. In addition, electrophysiological data from those patients with deeper VF defects (group 1) were compared with a normal control group. RESULTS: Twenty-six workers exhibited symptoms of erethism. The EMG showed sensorimotor polyneuropathy and multiple mononeuropathy. The VA was slightly affected in 48.27% (n = 14) of subjects. Loss of CS in at least one of four spatial frequencies and color vision alterations occurred in 96.5% (n = 28) and 44.8% (n = 13), respectively. VF alterations were identified in 72.4% (n = 21) patients. No morphologic changes were seen in the OCT scans. Latencies over 100 milliseconds and reduced amplitudes of P100 were found in the PRVEP (p < 0.05). The reduced amplitude of the b wave at the ffERG, of the P50 at the PERG and of the P1 wave at the mfERG results (p < 0.05) suggested that the outer retina was involved. Significant negative correlations among blood mercury levels, VA, and ffERG were observed. CONCLUSIONS: In this case series, showed that acute exposure to mercury vapor had a hazardous effect on the visual system. Although neurologic and visual pathway involvement was clearly demonstrated, the differences found compared to control support the existence of a direct functional retinal damage and participation in impaired vision in mercury poisoning.
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A major area in cancer therapy is the search for protective strategies against cisplatin-induced nephrotoxicity. We investigated the protective effect of cilastatin on cisplatin-induced injury to renal proximal tubular cells. Cilastatin is a specific inhibitor of renal dehydrodipeptidase I (DHP-I), which prevents hydrolysis of imipenem and its accumulation in the proximal tubule. Primary cultures of proximal cells were treated with cisplatin (1-30 microM) in the presence or absence of cilastatin (200 microg/ml). Apoptosis and mitochondrial injury were assessed by different techniques. Cisplatin uptake and DNA binding were measured by inductively coupled plasma spectrometry. HeLa cells were used to control the effect of cilastatin on the tumoricidal activity of cisplatin. Cisplatin increased cell death, apoptotic-like morphology, caspase activation, and mitochondrial injury in proximal tubular cells in a dose- and time-dependent way. Concomitant treatment with cilastatin reduced cisplatin-induced changes. Cilastatin also reduced the DNA-bound platinum but did not modify cisplatin-dependent up-regulation of death receptors (Fas) or ligands (tumor necrosis factor alpha, Fas ligand). In contrast, cilastatin did not show any effects on cisplatin-treated HeLa cells. Renal DHP-I was virtually absent in HeLa cells. Cilastatin attenuates cisplatin-induced cell death in proximal tubular cells without reducing the cytotoxic activity of cisplatin in tumor cells. Our findings suggest that the affinity of cilastatin for renal dipeptidase makes this effect specific for proximal tubular cells and may be related to a reduction in intracellular drug accumulation. Therefore, cilastatin administration might represent a novel strategy in the prevention of cisplatin-induced acute renal injury.
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Antineoplásicos/toxicidad , Cilastatina/farmacología , Cisplatino/toxicidad , Dipeptidasas/antagonistas & inhibidores , Túbulos Renales Proximales/efectos de los fármacos , Animales , Muerte Celular/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Cilastatina/metabolismo , ADN/metabolismo , Proteína Ligando Fas/biosíntesis , Proteína Ligando Fas/genética , Células HeLa , Humanos , Túbulos Renales Proximales/citología , Túbulos Renales Proximales/enzimología , Potencial de la Membrana Mitocondrial/efectos de los fármacos , ARN Mensajero/biosíntesis , Porcinos , Factor de Necrosis Tumoral alfa/biosíntesis , Factor de Necrosis Tumoral alfa/genética , Receptor fas/biosíntesis , Receptor fas/genéticaRESUMEN
Many individuals with seemingly normal hearing abilities struggle to understand speech in noisy backgrounds. To understand why this might be the case, we investigated the neural representation of speech in the auditory midbrain of gerbils with "hidden hearing loss" through noise exposure that increased hearing thresholds only temporarily. In noise-exposed animals, we observed significantly increased neural responses to speech stimuli, with a more pronounced increase at moderate than at high sound intensities. Noise exposure reduced discriminability of neural responses to speech in background noise at high sound intensities, with impairment most severe for tokens with relatively greater spectral energy in the noise-exposure frequency range (2-4 kHz). At moderate sound intensities, discriminability was surprisingly improved, which was unrelated to spectral content. A model combining damage to high-threshold auditory nerve fibers with increased response gain of central auditory neurons reproduced these effects, demonstrating that a specific combination of peripheral damage and central compensation could explain listening difficulties despite normal hearing thresholds.
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Pérdida Auditiva Provocada por Ruido/fisiopatología , Ruido/efectos adversos , Enmascaramiento Perceptual/fisiología , Percepción del Habla/fisiología , Estimulación Acústica , Animales , Cóclea/inervación , Cóclea/fisiopatología , Nervio Coclear/fisiopatología , Modelos Animales de Enfermedad , Gerbillinae , Audición/fisiología , Humanos , MasculinoRESUMEN
PURPOSE: Improve the quantity and quality of information obtained from traditional Loewenstein Occupational Therapy Cognitive Assessment Battery systems to monitor the evolution of patients' rehabilitation process as well as to compare different rehabilitation therapies. METHODS: The system replaces traditional artefacts with virtual versions of them to take advantage of cutting edge interaction technology. The system is defined as a Distributed User Interface (DUI) supported by a display ecosystem, including mobile devices as well as multi-touch surfaces. Due to the heterogeneity of the devices involved in the system, the software technology is based on a client-server architecture using the Web as the software platform. RESULTS: The system provides therapists with information that is not available (or it is very difficult to gather) using traditional technologies (i.e. response time measurements, object tracking, information storage and retrieval facilities, etc.). CONCLUSIONS: The use of DUIs allows therapists to gather information that is unavailable using traditional assessment methods as well as adapt the system to patients' profile to increase the range of patients that are able to take this assessment. Implications for Rehabilitation Using a Distributed User Interface environment to carry out LOTCAs improves the quality of the information gathered during the rehabilitation assessment. This system captures physical data regarding patient's interaction during the assessment to improve the rehabilitation process analysis. Allows professionals to adapt the assessment procedure to create different versions according to patients' profile. Improves the availability of patients' profile information to therapists to adapt the assessment procedure.
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Trastornos del Conocimiento/diagnóstico , Trastornos del Conocimiento/rehabilitación , Aplicaciones de la Informática Médica , Terapia Ocupacional/métodos , Evaluación de Resultado en la Atención de Salud , Interfaz Usuario-Computador , Humanos , Mejoramiento de la Calidad , Programas InformáticosRESUMEN
Periodicities in sound waveforms are widespread, and shape important perceptual attributes of sound including rhythm and pitch. Previous studies have indicated that, in the inferior colliculus (IC), a key processing stage in the auditory midbrain, neurons tuned to different periodicities might be arranged along a periodotopic axis which runs approximately orthogonal to the tonotopic axis. Here we map out the topography of frequency and periodicity tuning in the IC of gerbils in unprecedented detail, using pure tones and different periodic sounds, including click trains, sinusoidally amplitude modulated (SAM) noise and iterated rippled noise. We found that while the tonotopic map exhibited a clear and highly reproducible gradient across all animals, periodotopic maps varied greatly across different types of periodic sound and from animal to animal. Furthermore, periodotopic gradients typically explained only about 10% of the variance in modulation tuning between recording sites. However, there was a strong local clustering of periodicity tuning at a spatial scale of ca. 0.5 mm, which also differed from animal to animal.
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Vías Auditivas/fisiología , Mapeo Encefálico , Análisis por Conglomerados , Colículos Inferiores/fisiología , Periodicidad , Localización de Sonidos/fisiología , Estimulación Acústica , Animales , Percepción Auditiva/fisiología , Gerbillinae , Colículos Inferiores/citología , Potenciales de la Membrana/fisiología , Neuronas/fisiología , Psicofísica , Factores de TiempoRESUMEN
Mice are of paramount importance in biomedical research and their vocalizations are a subject of interest for researchers across a wide range of health-related disciplines due to their increasingly important value as a phenotyping tool in models of neural, speech and language disorders. However, the mechanisms underlying the auditory processing of vocalizations in mice are not well understood. The mouse audiogram shows a peak in sensitivity at frequencies between 15-25 kHz, but weaker sensitivity for the higher ultrasonic frequencies at which they typically vocalize. To investigate the auditory processing of vocalizations in mice, we measured evoked potential, single-unit, and multi-unit responses to tones and vocalizations at three different stages along the auditory pathway: the auditory nerve and the cochlear nucleus in the periphery, and the inferior colliculus in the midbrain. Auditory brainstem response measurements suggested stronger responses in the midbrain relative to the periphery for frequencies higher than 32 kHz. This result was confirmed by single- and multi-unit recordings showing that high ultrasonic frequency tones and vocalizations elicited responses from only a small fraction of cells in the periphery, while a much larger fraction of cells responded in the inferior colliculus. These results suggest that the processing of communication calls in mice is supported by a specialization of the auditory system for high frequencies that emerges at central stations of the auditory pathway.
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Vías Auditivas/fisiología , Percepción Auditiva/fisiología , Potenciales Evocados Auditivos del Tronco Encefálico/fisiología , Colículos Inferiores/fisiología , Vocalización Animal/fisiología , Animales , Nervio Coclear/fisiología , Núcleo Coclear/fisiología , Ratones , Ondas UltrasónicasRESUMEN
It is widely accepted that through a process of adaptation cells adjust their sensitivity in accordance with prevailing stimulus conditions. However, in two recent studies exploring adaptation in the rodent inferior colliculus and somatosensory cortex, neurons did not adapt towards global mean, but rather became most sensitive to inputs that were located towards the edge of the stimulus distribution with greater intensity than the mean. We re-examined electrophysiological data from the somatosensory study with the purpose of exploring the underlying encoding strategies. We found that neural gain tended to decrease as stimulus variance increased. Following adaptation to changes in global mean, neuronal output was scaled such that the relationship between firing rate and local, rather than global, differences in stimulus intensity was maintained. The majority of cells responded to large, positive deviations in stimulus amplitude; with a small number responding to both positive and negative changes in stimulus intensity. Adaptation to global mean was replicated in a model neuron by incorporating both spike-rate adaptation and tonic-inhibition, which increased in proportion to stimulus mean. Adaptation to stimulus variance was replicated by approximating the output of a population of neurons adapted to global mean and using it to drive a layer of recurrently connected depressing synapses. Within the barrel cortex, adaptation ensures that neurons are able to encode both overall levels of variance and large deviations in the input. This is achieved through a combination of gain modulation and a shift in sensitivity to intensity levels that are greater than the mean.
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Potenciales de Acción/fisiología , Adaptación Fisiológica/fisiología , Células Receptoras Sensoriales/fisiología , Corteza Somatosensorial/fisiología , Animales , Modelos Neurológicos , Ratas , Ratas Long-Evans , Corteza Somatosensorial/citología , Sinapsis/fisiologíaRESUMEN
We have previously shown that neurons in primary auditory cortex (A1) of anaesthetized (ketamine/medetomidine) ferrets respond more strongly and reliably to dynamic stimuli whose statistics follow "natural" 1/f dynamics than to stimuli exhibiting pitch and amplitude modulations that are faster (1/f(0.5)) or slower (1/f(2)) than 1/f. To investigate where along the central auditory pathway this 1/f-modulation tuning arises, we have now characterized responses of neurons in the central nucleus of the inferior colliculus (ICC) and the ventral division of the mediate geniculate nucleus of the thalamus (MGV) to 1/f(γ) distributed stimuli with γ varying between 0.5 and 2.8. We found that, while the great majority of neurons recorded from the ICC showed a strong preference for the most rapidly varying (1/f(0.5) distributed) stimuli, responses from MGV neurons did not exhibit marked or systematic preferences for any particular γ exponent. Only in A1 did a majority of neurons respond with higher firing rates to stimuli in which γ takes values near 1. These results indicate that 1/f tuning emerges at forebrain levels of the ascending auditory pathway.
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Vías Auditivas/fisiología , Estimulación Acústica , Animales , Electrofisiología , Hurones , Colículos Inferiores/fisiología , Neuronas/fisiología , Tálamo/fisiologíaRESUMEN
Neurons in primary auditory cortex (A1) are known to exhibit a phenomenon known as stimulus-specific adaptation (SSA), which means that, when tested with pure tones, they will respond more strongly to a particular frequency if it is presented as a rare, unexpected "oddball" stimulus than when the same stimulus forms part of a series of common, "standard" stimuli. Although SSA has occasionally been observed in midbrain neurons that form part of the paraleminscal auditory pathway, it is thought to be weak, rare, or nonexistent among neurons of the leminscal pathway that provide the main afferent input to A1, so that SSA seen in A1 is likely generated within A1 by local mechanisms. To study the contributions that neural processing within the different cytoarchitectonic layers of A1 may make to SSA, we recorded local field potentials in A1 of the rat in response to standard and oddball tones and subjected these to current source density analysis. Although our results show that SSA can be observed throughout all layers of A1, right from the earliest part of the response, there are nevertheless significant differences between layers, with SSA becoming significantly stronger as stimulus-related activity passes from the main thalamorecipient layers III and IV to layer V.
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Adaptación Fisiológica/fisiología , Corteza Auditiva/fisiología , Percepción Auditiva/fisiología , Variación Contingente Negativa/fisiología , Potenciales Evocados Auditivos/fisiología , Estimulación Acústica/métodos , Animales , Vías Auditivas/fisiología , Electroencefalografía/métodos , Femenino , Mesencéfalo/citología , Neuronas/fisiología , Psicofísica , Ratas , Ratas Long-EvansRESUMEN
The responses of neurons within the primary auditory cortex (A1) of the ferret elicited by broadband dynamic spectral ripple stimuli were examined over a range of ripple spectral densities and ripple velocities. The large majority of neurons showed modulated responses to these stimuli and responded most strongly at low ripple densities and velocities. The period histograms of their responses were subjected to Fourier analysis, and the ratio of the magnitudes of the f1 and fo (DC) components of these responses were calculated to give a quantitative index of response linearity. For 82 out of 396 neurons tested (20.7%) this ratio remained above 1.0 over the entire range of ripple densities and velocities. These neurons were classified as 'consistently linear'. A further 134/396 (33.8%) of neurons maintained an f1/f0 ratio above 1.0 for either a range of ripple densities at a fixed ripple velocity, or over a range of ripple velocities at a specific ripple density, and were classified as 'locally linear'. Interestingly, for the superficial layers of the primary auditory cortex, consistently linear and locally linear neurons outnumbered nonlinear neurons by a 2:1 ratio. The converse was true for the deep layers. Unlike in primary visual cortex, where f1/f0 ratios have been reported to exhibit a bimodal distribution with a minimum at f1/f0 = 1, f1/f0 ratios for A1 are unimodally distributed with a peak at f1/f0 = 1.