posted on 2011-12-07, 09:52authored byNadia Pilati
Acoustic over exposure (AOE) triggers hearing loss and tinnitus but
cellular mechanisms underlying those auditory defects are still poorly
understood. This thesis explores the changes of excitability produced by AOE in
identified cells of the rat dorsal cochlear nucleus (DCN) within the auditory
brainstem. A development of a method combining Golgi silver impregnation with
Nissl staining allowed study of the morphology and the distribution of the main
DCN neuronal subtypes within slices containing the DCN. Whole cell patch
clamp recordings allowed characterisation of the distinctive electrophysiological
properties of the main DCN neuronal subtypes. In vitro stimulations of auditory
or multisensory synaptic inputs showed fundamental differences in terms of the
principal neurones firing pattern and the role of inhibitory synaptic transmission
on firing pattern.
Wistar rats were exposed to loud (110 dB SPL) single tones (15 kHz) for
a period of 4 hours (protocol of AOE). Non invasive auditory brainstem
response recordings were performed after 3 to 4 days and showed a significant
increase of the rat’s hearing threshold for frequencies above 8 kHz. Whole cell
recordings performed at a similar time (3 to 4 days) after AOE, showed that
AOE led to a change of the passive and the active properties of DCN
interneurones and principal cells. AOE also decreased the general excitability of
the cellular network and affected differently excitatory and inhibitory synaptic
transmission onto principal neurones depending on whether multisensory or
auditory synaptic inputs were stimulated. Computational modelling allowed
simulation of the effects of AOE on principal cell firing patterns and elaboration
of a general theory whereby AOE triggers shifts of hearing thresholds
concomitant with plastic adjustments in the DCN network.
In conclusion, an elevation of the hearing threshold accompanied by
significant excitability changes within the central auditory system could
represent fundamental steps towards the development of tinnitus.