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      Acute effects and after-effects of acoustic coordinated reset neuromodulation in patients with chronic subjective tinnitus

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          Abstract

          Chronic subjective tinnitus is an auditory phantom phenomenon characterized by abnormal neuronal synchrony in the central auditory system. As shown computationally, acoustic coordinated reset (CR) neuromodulation causes a long-lasting desynchronization of pathological synchrony by downregulating abnormal synaptic connectivity. In a previous proof of concept study acoustic CR neuromodulation, employing stimulation tone patterns tailored to the dominant tinnitus frequency, was compared to noisy CR-like stimulation, a CR version significantly detuned by sparing the tinnitus-related pitch range and including substantial random variability of the tone spacing on the frequency axis. Both stimulation protocols caused an acute relief as measured with visual analogue scale scores for tinnitus loudness (VAS-L) and annoyance (VAS-A) in the stimulation-ON condition (i.e. 15 min after stimulation onset), but only acoustic CR neuromodulation had sustained long-lasting therapeutic effects after 12 weeks of treatment as assessed with VAS-L, VAS-A scores and a tinnitus questionnaire (TQ) in the stimulation-OFF condition (i.e. with patients being off stimulation for at least 2.5 h). To understand the source of the long-lasting therapeutic effects, we here study whether acoustic CR neuromodulation has different electrophysiological effects on oscillatory brain activity as compared to noisy CR-like stimulation under stimulation-ON conditions and immediately after cessation of stimulation. To this end, we used a single-blind, single application, cross over design in 18 patients with chronic tonal subjective tinnitus and administered three different 16-minute stimulation protocols: acoustic CR neuromodulation, noisy CR-like stimulation and low frequency range (LFR) stimulation, a CR type stimulation with deliberately detuned pitch and repetition rate of stimulation tones, as control stimulation. We measured VAS-L and VAS-A scores together with spontaneous EEG activity pre-, during- and post-stimulation. Under stimulation-ON conditions acoustic CR neuromodulation and noisy CR-like stimulation had similar effects: a reduction of VAS-L and VAS-A scores together with a decrease of auditory delta power and an increase of auditory alpha and gamma power, without significant differences. In contrast, LFR stimulation had significantly weaker EEG effects and no significant clinical effects under stimulation-ON conditions. The distinguishing feature between acoustic CR neuromodulation and noisy CR-like stimulation were the electrophysiological after-effects.

          Acoustic CR neuromodulation caused the longest significant reduction of delta and gamma and increase of alpha power in the auditory cortex region. Noisy CR-like stimulation had weaker and LFR stimulation hardly any electrophysiological after-effects. This qualitative difference further supports the assertion that long-term effects of acoustic CR neuromodulation on tinnitus are mediated by a specific disruption of synchronous neural activity. Furthermore, our results indicate that acute electrophysiological after-effects might serve as a marker to further improve desynchronizing sound stimulation.

          Highlights

          • Acute effects and acute after-effects of dedicated tinnitus sound therapy are studied with EEG.

          • Sound therapy causing long-lasting, sustained effects causes pronounced acute after-effects.

          • Acute EEG after-effects might serve as marker to develop desynchronizing sound therapy.

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          Most cited references61

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Regulation of synaptic efficacy by coincidence of postsynaptic APs and EPSPs.

            Activity-driven modifications in synaptic connections between neurons in the neocortex may occur during development and learning. In dual whole-cell voltage recordings from pyramidal neurons, the coincidence of postsynaptic action potentials (APs) and unitary excitatory postsynaptic potentials (EPSPs) was found to induce changes in EPSPs. Their average amplitudes were differentially up- or down-regulated, depending on the precise timing of postsynaptic APs relative to EPSPs. These observations suggest that APs propagating back into dendrites serve to modify single active synaptic connections, depending on the pattern of electrical activity in the pre- and postsynaptic neurons.
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              Long-lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path.

              1. The after-effects of repetitive stimulation of the perforant path fibres to the dentate area of the hippocampal formation have been examined with extracellular micro-electrodes in rabbits anaesthetized with urethane.2. In fifteen out of eighteen rabbits the population response recorded from granule cells in the dentate area to single perforant path volleys was potentiated for periods ranging from 30 min to 10 hr after one or more conditioning trains at 10-20/sec for 10-15 sec, or 100/sec for 3-4 sec.3. The population response was analysed in terms of three parameters: the amplitude of the population excitatory post-synaptic potential (e.p.s.p.), signalling the depolarization of the granule cells, and the amplitude and latency of the population spike, signalling the discharge of the granule cells.4. All three parameters were potentiated in 29% of the experiments; in other experiments in which long term changes occurred, potentiation was confined to one or two of the three parameters. A reduction in the latency of the population spike was the commonest sign of potentiation, occurring in 57% of all experiments. The amplitude of the population e.p.s.p. was increased in 43%, and of the population spike in 40%, of all experiments.5. During conditioning at 10-20/sec there was massive potentiation of the population spike (;frequency potentiation'). The spike was suppressed during stimulation at 100/sec. Both frequencies produced long-term potentiation.6. The results suggest that two independent mechanisms are responsible for long-lasting potentiation: (a) an increase in the efficiency of synaptic transmission at the perforant path synapses; (b) an increase in the excitability of the granule cell population.
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                Author and article information

                Contributors
                Journal
                Neuroimage Clin
                Neuroimage Clin
                NeuroImage : Clinical
                Elsevier
                2213-1582
                28 May 2017
                2017
                28 May 2017
                : 15
                : 541-558
                Affiliations
                [a ]Institute of Neuroscience and Medicine–Neuromodulation (INM-7), Jülich Research Center, Jülich 52428, Germany
                [b ]Jean-Uhrmacher-Institute for Clinical ENT-Research, University of Cologne, Geibelstraße 29-31, Cologne 50931, Germany
                [c ]Department of Otorhinolaryngology, Head and Neck Surgery, Audiology and Pediatric Audiology, University of Cologne, Kerpener Str. 62, Cologne 50937, Germany
                [d ]Department of Psychiatry and Psychotherapy, University of Regensburg, Bezirksklinikum, Universitätsstraße 84, Regensburg 93053, Germany
                [e ]Interdisciplinary Tinnitus Center, University of Regensburg, Regensburg, Germany
                [f ]Pharmaplex bvba, Avenue Saint-Hubert 51, Wezembeek-Oppem 1970, Belgium
                [g ]Department of Neurosurgery, Stanford University, 300 Pasteur Drive, Stanford, CA 94305-5327, USA
                [h ]Department of Neuromodulation, University of Cologne, Gleueler Straße 176-178, Cologne 50935, Germany
                Author notes
                [* ]Corresponding author at: Department of Neurosurgery, Stanford University School of Medicine, Stanford, CA 94305, USA.Department of NeurosurgeryStanford University School of MedicineStanfordCA94305USA ptass@ 123456stanford.edu
                Article
                S2213-1582(17)30122-5
                10.1016/j.nicl.2017.05.017
                5476468
                28652968
                9d2e48ba-0732-42fe-bc3a-ad1a0f6849da
                © 2017 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 28 November 2016
                : 21 May 2017
                : 22 May 2017
                Categories
                Regular Article

                alpha band activity,coordinated reset neuromodulation,delta band activity,electroencephalography,gamma band activity

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