Abstract

Noise overstimulation can induce loss of synaptic ribbons associated with loss of Inner Hair Cell – Auditory Nerve synaptic connections. This study examined if systemic administration of Piribedil, a dopamine agonist that reduces the sound evoked auditory nerve compound action potential and/or Memantine, an NMDA receptor open channel blocker, would reduce noise-induced loss of Inner Hair Cell ribbons. Rats received systemic Memantine and/or Piribedil for 3 days before and 3 days after a 3 hour 4 kHz octave band noise at 117 dB (SPL). At 21 days following the noise there was a 26% and 38% loss of synaptic ribbons in regions 5.5 and 6.5 mm from apex, respectively, elevations in 4-, 8- and 20 kHz tonal ABR thresholds and reduced dynamic output at higher intensities of stimulation. Combined treatment with Piribedil and Memantine produced a significant reduction in the noise-induced loss of ribbons in both regions and changes in ABR sensitivity and dynamic responsiveness. Piribedil alone gave significant reduction in only the 5.5 mm region and Memantine alone did not reach significance in either region. Results identify treatments that could prevent the hearing loss and hearing disorders that result from noise-induced loss of Inner Hair Cell – Auditory Nerve synaptic connections.

Highlights

  • Treatment with just Piribedil gave a significant reduction in the loss in the 5.5 mm region (p < 0.05) and a trend towards reduction in the 6.5 mm region

  • A result of the current study, finding systemic Piribedil can reduce the noise-induced loss of IHC ribbons, is consistent with an earlier study using intrascalar application of Piribedil during a noise exposure that found a reduced bursting of auditory nerve peripheral processes[2,11,12]

  • The present study showed Piribedil treatment produced a significant reduction in ribbon loss only in the region 5.5 mm from apex, while in the region 6.5 mm from apex the reduction was not sufficient to reach significance

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Summary

Results

Inner Hair Cell – Auditory Nerve Synaptic Ribbons. Figure 1 shows a representative image of CTBP2 immunolabeling of IHC synaptic ribbons in a noise exposed animal without drug treatment. In the group of animals receiving a combined Piribedil and Memantine treatment the mean number of synaptic ribbons per IHC was 18.2 +/− 1.5 This was significantly greater than the mean in untreated noise exposed animals (p < 0.05) and was not significantly different than the mean number in non-exposed, normal rats (Fig. 3A). The group of rats receiving treatment with Piribedil alone had a mean number of synaptic ribbons per IHC of 21.1 +/− 1.3, a significant increase (p < 0.01) over the number found in the noise exposed without drug treatment group and not significantly different from normal. In the group of animals receiving a combined Piribedil and Memantine treatment the mean number of synaptic ribbons per IHC was 20.8 +/− 1.0 This was significantly greater than the mean in untreated noise exposed animals (p < 0.01) and was not significantly different than the mean number in normal rats (Fig. 3B). There was a significant difference (p ≤ 0.01) between Piribedil +Memantine treatment vs. Memantine alone at all frequencies and Piribedil alone at 4 & 8 kHz

Discussion
C: Noise - Piribedil only
Methods
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