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Verschooten, E.

Publications and source records attributed to Verschooten, E..

2 recordsLinked to original sources

Assessment of Contralateral Efferent Effects in Human Via ECochG

Efferent projections from the brainstem to the inner ear are well-described anatomically and physiologically but their precise function remains debated. The medial olivocochlear (MOC) system and its reflex, the MOCR, have been particularly well studied. In animals, anatomical and physiological data are fine-grained and extensive and suggest an important role for the MOCR in anti-masking e.g. to improve the detection of tones in background noise. Extensive behavioral studies in human support this role, but direct linking of behavioral paradigms to the MOCR is challenging because of the difficulty in obtaining appropriate human neural measures. We developed a new approach in which mass potentials were recorded near the cochlea of normal hearing and awake human volunteers to increase the signal-to-noise (SNR) ratio, and examined whether broadband noise to the contralateral ear elicited MOCR anti-masking effects as reported in animals. Probing the mass potential to the onset of brief tones at 4 and 6 kHz, convincing anti-masking or suppressive effects consistent with the MOCR were not detected. We then changed the recording technique to examine the neural phase-locked contribution to the mass potential in response to long, low-frequency tones, and found that contralateral sound suppressed neural responses in a systematic and progressive manner. We followed up with psychophysical experiments in which we found that contralateral noise elevated detection threshold for tones up to 4 kHz. Our study provides a new way to study efferent effects in the human peripheral auditory system and shows that contralateral efferent effects are biased towards low frequencies.

neuroscience↗

Intrinsic mechanical sensitivity of auditory neurons as a contributor to sound-driven neural activity

Mechanosensation - by which mechanical stimuli are converted into a neuronal signal - is the basis for the sensory systems of hearing, balance, and touch. Mechanosensation is unmatched in speed and its diverse range of sensitivities, reaching its highest temporal limits with the sense of hearing; however, hair cells (HCs) and the auditory nerve (AN) serve as obligatory bottlenecks for sounds to engage the brain. Like other sensory neurons, auditory neurons use the canonical pathway for neurotransmission and millisecond-duration action potentials (APs). How the auditory system utilizes the relatively slow transmission mechanisms to achieve ultrafast speed and high audio-frequency hearing remains an enigma. Here, we address this paradox and report that the AN is mechanically sensitive, and minute mechanical displacement profoundly affects its response properties. Sound-mimicking sinusoidal mechanical and electrical current stimuli affect phase-locked responses. In a phase-dependent manner, the two stimuli can also evoke suppressive responses. We propose that mechanical sensitivity interacts with synaptic responses to shape responses in the AN, including frequency tuning and temporal phase-locking. The combination of neurotransmission and mechanical sensation to control spike patterns gives the AN a secondary receptor role, an emerging theme in primary neuronal functions.

neuroscience↗