Our ability to discriminate and recognize human voices is amongst the most important functions of the human auditory system. The current study sought to determine whether electrophysiological markers could be used as objective measures of voice familiarity, by looking at the electrophysiological responses [mismatch negativity (MMN) and P3a] when the infrequent stimulus presented is a familiar voice as opposed to an unfamiliar voice. Results indicate that the MMN elicited by a familiar voice is greater than that elicited by an unfamiliar voice at FCz. The familiar voice also produced a greater P3a wave than that triggered by the unfamiliar voice at Fz. As both the MMN and the P3a were elicited as participants were instructed not to pay attention to incoming stimulation, these findings suggest that voice recognition is a particularly potent preattentive process whose neural representations can be objectively described through electrophysiological assessments.
There are important developmental changes occurring during infancy in visual cortical structures that underlie higher-order perceptual abilities. Using high-density electrophysiological recording techniques, the present study aimed to examine the development of visual mechanisms, during the first year of life, associated with texture segregation. Forty-two normal full term infants were tested at 1, 3, 6 or 12 months of age. Visual-evoked potentials to low-level stimuli varying in orientation (oriVEP) and higher-level textured stimuli (texVEP) were recorded from 128 scalp electrodes. Difference potentials were obtained to extract the VEP component associated specifically with texture segregation (tsVEP). Results show a clear developmental pattern regarding amplitude, latency and scalp distribution of tsVEP, which appears at around 3 months but does not reach maturity by 12 months of age. A reduction in latency is particularly evident between 3 and 6 months, whereas amplitude shows a gradual increase with a marked increment between 3 and 6 months for low-level orientation stimuli and between 6 and 12 months for higher-level textured stimuli. These developmental patterns are attributed to neural maturational processes such as myelination and synaptogenesis. The differential developmental rates can be explained by delayed maturational processes of brain regions involved in more complex visual processing.
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