Effects of electrical stimulation of efferent olivocochlear neurons on cat auditory-nerve fibers. II. Spontaneous rate

Abstract

In order to increase our understanding of cochlear mechanisms, we measured changes in the rate of spontaneous firing (SR) of single auditory-nerve fibers in response to the stimulation of medial olivocochlear efferents in cats. During the first second of efferent stimulation, SR was depressed by up to 35%, except in one very sensitive animal in which depressions up to 80% were found. With data from this aberrant cat excluded, the SR depression, on the average, increased as auditory-nerve fiber sensitivity increased, increased as the original SR decreased (data were not obtained for SRs less than two spikes/sec), and had a broad maximum at CFs of about 10 kHz. After the efferent stimulation was turned off, there was an “overshoot” in which the SR increased past the original rate in some fibers. The “overshoot” was larger for fibers with lower SRs and for fibers which showed larger “adaptation” in the efferent-induced depression of SR. The data on SR depression during efferent stimulation are consistent with two hypotheses: (1) that the stronger than usual efferent suppression of “spontaneous” rate found in some very sensitive fibers occurs because the “spontaneous” firing was, in part, a response to sound, and (2) that “true spontaneous” firing is reduced by the efferent-induced hyperpolarization of outer hair cells (OHCs) being electrically coupled through the endocochlear potential to inner hair cells (IHCs). It is suggested that (1) the efferent-induced suppression of “true spontaneous” activity is largest at CFs near 10 kHz because this CF region receives the greatest OHC innervation from medial efferents and the efferent-induced change in OHCs is electrically coupled to IHCs, whereas (2) the efferent suppression of responses to sound is largest at lower CFs because the efferent endings on OHCs act to decrease the motion of the basilar membrane and this change is propagated apically from the active efferent synapses on OHCs.