Emergence of Behavioral Tinnitus in Gerbils Is Associated with Reduced Spontaneous Rates in Single Auditory Nerve Fibers.

Tinnitus is often initiated by damage to the peripheral auditory system, for example, by acoustic overexposure. Animal studies have shown that such noise-induced tinnitus is related to increased spontaneous activity in the dorsal cochlear nucleus as well as further along the central auditory pathway. However, the role of spontaneous activity of the auditory nerve, connecting the peripheral and central auditory systems, in tinnitus emergence remains unknown. In the current study, tinnitus was induced by exposing anesthetized Mongolian gerbils of either sex to a 115 dB SPL narrowband noise. After one day of recovery, animals were behaviorally tested for gap detection deficits using a gap-prepulse inhibition of the acoustic startle reflex (GPIAS) paradigm, indicative of tinnitus. Noise-induced threshold shifts did not differ between animals with and without signs of tinnitus. Interestingly, single auditory nerve fibers recorded from animals with signs of tinnitus had significantly reduced spontaneous rates compared with both noise-exposed animals without signs of tinnitus and sham-exposed animals. Furthermore, spontaneous rate reduction was specific to fibers tuned to frequencies within the frequency bands that showed gap detection deficits. On the other hand, interspike interval variability and bursting behavior increased in fibers from noise-exposed compared with sham-exposed animals but did not differ with gap detection deficits. These findings suggest that tinnitus-related central hyperactivity may be initiated by reduced spontaneous rates of its innervating auditory nerve fibers. This is consistent with current theoretical models explaining the central manifestation of tinnitus and offers a more detailed definition of tinnitus-related deafferentation.