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Morgan Thienpont

Publications and source records attributed to Morgan Thienpont.

2 recordsLinked to original sources

Computational Auditory Periphery Models: the Return of the Rodent

Animal experiments have provided many insights on auditory function, notably in cases of sensorineural hearing loss (SNHL). However, it is not always clear how these findings translate to the human auditory system in clinically relevant contexts. Cross-species computational models of the auditory periphery can help bridge the gap between non-invasive human diagnostics and experimental evidence from animal studies. In this work we adapted a 1-D nonlinear cochlear transmission-line model designed for the human auditory periphery to mouse and gerbil, enabling a single computational framework for cross-species research on SNHL. Species-specific anatomical and physiological parameters - including basilar membrane (BM) length and width, stapes area, middle-ear transfer functions, and frequency range - were adjusted to match each species' auditory periphery and hearing range. Other cochlear parameters were calibrated to reproduce realistic cochlear tuning and compression. The adapted mouse and gerbil models were validated against experimental BM velocity level-growth characteristics, auditory-nerve (AN) tuning curves, and DPOAEs. Simulated AN outputs reasonably matched empirical measurements, including realistic AN thresholds and frequency selectivity. However, the discrepancy between simulations and measurements became larger for cochlear sections closer to the base or apex. Simulations of cochlear synaptopathy reproduced observed differences in recorded auditory brainstem and envelope following responses from mice and gerbils with SNHL. OHC individualization of the mouse model based on DPOAEs failed to faithfully reproduce individual measurements, although intergroup differences in OHC damage were captured. Our findings demonstrate that biophysically grounded auditory models can be translated across species while preserving realistic sound-coding properties and pathophysiological alterations.

q-bio.NC

Short-wave admittance correction for a time-domain cochlear transmission line model

Transmission line (TL) models implemented in the time domain can efficiently simulate basilar-membrane (BM) displacement in response to transient or non-stationary sounds. By design, a TL model is well-suited for an one-dimensional (1-D) characterization of the traveling wave, but the real configuration of the cochlea also introduces higher-dimensional effects. Such effects include the focusing of the pressure around the BM and transverse viscous damping, both of which are magnified in the short-wave region. The two effects depend on the wavelength and are more readily expressed in the frequency domain. In this paper, we introduce a numerical correction for the BM admittance to account for 2-D effects in the time domain using autoregressive filtering and regression techniques. The correction was required for the implementation of a TL model tailored to the gerbil cochlear physiology. The model, which includes instantaneous nonlinearities in the form of variable damping, initially presented insufficient compression with increasing sound levels. This limitation was explained by the strong coupling between gain and frequency selectivity assumed in the 1-D nonlinear TL model, whereas cochlear frequency selectivity shows only a moderate dependence on sound level in small mammals. The correction factor was implemented in the gerbil model and made level-dependent using a feedback loop. The updated model achieved some decoupling between frequency selectivity and gain, providing 5 dB of additional gain and extending the range of sound levels of the compressive regime by 10 dB. We discuss the relevance of this work through two key features: the integration of both analytical and regression methods for characterizing BM admittance, and the combination of instantaneous and non-instantaneous nonlinearities.

eess.AS