Age related changes to the dynamics of contralateral DPOAE suppression in human subjects
© Konomi et al.; licensee BioMed Central Ltd. 2014
Received: 27 January 2014
Accepted: 11 June 2014
Published: 16 June 2014
The two ears are linked with a neural pathway such that stimulation of one ear has a modulating effect on the contralateral cochlea. This is mediated by cochlear afferent neurons connecting with olivo-cochlear efferents. The monitoring of this pathway is easily achieved by measuring contralateral suppression of otoacoustic emissions, and there is some clinical value in the ability to assess the integrity of this pathway. An important step in an evaluation of clinical utility is to assess any age-related changes. Accordingly, in the present study we measure the dynamics of contralateral DPOAE suppression in a population of normal hearing subjects of different ages.
Using a real-time DPOAE recording method we assessed contralateral DPOAE suppression in 95 ears from 51 subjects (age range 2–52 years). DPOAE (2f1-f2; f2 = 4.4 kHz; f2/f1 = 1.22) input–output functions were measured. In response to contralateral broadband noise, dynamic aspects of DPOAE suppression were measured, specifically suppression onset latency and time constants.
An age-related reduction in DPOAE amplitudes was observed. Both the detectability and the degree of contralateral DPOAE suppression were decreased in older age groups. We find an age-related increase in the latency of onset of DPOAE suppression to contralateral stimulation, but no significant change in suppression time-constants.
Olivo-cochlear function as revealed by contralateral suppression of DPOAEs shows some important age-related changes. In addition to reduced emissions (outer haircell suppression) we find an increased latency that may reflect deterioration in auditory brainstem function. Regarding clinical utility, it is possible that the changes observed may reflect an aspect of age-related hearing loss that has not been previously considered.
Otoacoustic emission (OAE) recording has become an important clinical tool for objective testing of cochlear function, in particular to verify the integrity of the outer haircell system. Distortion product otoacoustic emissions (DPOAEs)  are widely used for neonatal screening and other diagnostic purposes in infants, but appear to be less useful in adult testing. In part this is due to an age-related decline in OAEs that has been demonstrated in a number of human and animal model studies [2–8]. The outer haircell system that generates OAE signals can be modulated by activity in olivo-cochlear efferents originating in the superior olivary complex of the brainstem [9, 10]. An olivo-cochlear “reflex” can be activated by contralateral acoustic stimulation, which typically inhibits outer haircells, and causes OAE suppression. Many authors have reported on contralateral suppression of DPOAEs in human studies and in animal models [11–14] and have speculated on potential clinical applications [15, 16]. It has been suggested that this brainstem reflex may have diagnostic value because the pathways involved include both cochlear afferents and efferents, as well as inner and outer haircell systems. However, contralateral DPOAE suppression appears to have age related deterioration [17–21] that could be a limitation on clinical utility. On the other hand, such deterioration may reveal important age related effects of clinical diagnostic value.
In our previous studies of contralateral DPOAE suppression or modulation [14, 16, 22, 23] we have used real-time recording of DPOAE signals in order to quantify the dynamics of DPOAE changes that result from contralateral acoustic stimulation. In the present study, in normal hearing human subjects, we report on age related changes in these dynamic aspects including the onset latency and time constants of DPOAE suppression. Specifically we report an age-related reduction in DPOAE suppression to contralateral stimulation, and also an age-related increase in the latency of onset of DPOAE suppression.
DPOAE levels and the effects of contralateral acoustic stimulation were determined in 95 ears from 51 randomly chosen subjects across a wide age range (2 – 52 years) with no history of sensorineural or conductive hearing loss. We did not formally assess audiometric thresholds and did not exclude subjects because of hearing status because our aim was to assess DPOAE suppression dynamics in the general population. We divided our subjects into five age groups as follows: 1–10 years, 13 subjects (24 ears); 11–20 years, 14 subjects (26 ears); 21–30 years, 8 subjects (15 ears); 31–40 years, 10 subjects (19 ears), > 41 years, 6 subjects (11 ears). This study was approved by the Research Ethics Board at the Hospital for Sick Children, Toronto, and was carried out with the consent of adult participants or parents of children prior to testing.
Measurement of real-time DPOAE suppression
DPOAEs were recorded in real-time using a custom research device (Vivo 600DPR; Vivosonic, Toronto, Ontario, Canada). The device uses narrow bandpass digital filtering and signal modeling to determine DPOAE levels in real-time with a temporal resolution of <2 ms . All recordings were made in a sound-attenuating room. The DPOAE was determined from the 2f1-f2 distortion product (f2=4.4 kHz; f2/f1 = 1.22; L1 = L2 -10 dB). The stimulus levels used for DPOAE recording were adjusted for each subject based on individual input–output (I/O) functions. Thus, I/O functions were recorded with f2=4.4 kHz, at levels of L2 from 50 - 70 dB SPL, and the stimulus level chosen was that resulting in a DPOAE signal at 0.5 – 0.7 of maximum level . Contralateral stimulation was a 0.5 s duration broadband noise at 50 dB SPL intermittently presented every 1.5 s. This signal was generated by Adobe Audition software (Adobe Systems Inc., San Jose, CA) and presented via an Etymotic Research ER-2 transducer (Etymotic Research, Elk Gorge Village, IL).
DPOAE data analysis
For each ear we have measured baseline DPOAE levels, and then in response to contralateral stimulation the amplitude of DPOAE suppression, and the dynamic aspects, specifically the onset latency and time constants of suppression. The suppression onset latency was measured as the interval between the onset of contralateral noise stimulus and the initial change point in DPOAE calculated from the intercept of linear regressions plotted through the baseline and first part of the suppression response . Occasionally a very large (by an order of magnitude) DPOAE suppression was observed, caused by a middle ear muscle reflex. These artifacts were excluded from the data before analysis . Tests for statistical significance were made with SPSS software (Sigma Plot 11.2; SPSS Inc., Chicago, IL). Fisher exact test was used in the comparison of presence rate of DPOAE suppression in each age group. Correlation coefficients were determined using Pearson product moment correlation.
DPOAE amplitude with age
Dynamics (DPOAE suppression onset latency and time constants) and amplitude of contralateral DPOAE suppression in different age groups
Age group (years)
Suppression amplitude (dB)
Onset latency (ms)
Onset time constants (ms)
neonates (<3 month)
-6.7 to 15 (week)
1 - 10
11 - 20
21 - 30
31 - 40
Contralateral DPOAE suppression with age
Age-related changes in DPOAE suppression dynamics
Degradation of DPOAE with age
Previous reports have described a reduction in amplitudes of OAEs with aging [4–8, 25]. In addition it has been reported that the rate of spontaneous OAEs is lower in elder subjects . In the present study, DPOAE amplitudes decreased with age similar to that reported in previous work. There has been much discussion about the possible causes of age-related declines and it is likely that many factors contribute. These include loss of sensory cells, degeneration of stria vascularis, and reduction in the endolymphatic potential. Other more central causes of presbycusis such as loss of spiral ganglion cells [27, 28] logically do not contribute directly to reduction in outer haircell generated OAEs (although there could conceivable be some indirect effects). Some animal studies of presbycusis have shown that functional hearing loss precedes or is greater than expected from haircell decrements [3, 29]. This suggests that perhaps OAE reductions have non-sensory cell origins such as strial degeneration or the degradation of tectorial and basilar membrane integrity.
Aging of olivo-cochlear function
Recent studies have reported a degradation of contralateral suppression of transient evoked OAE in human with advancing age [30, 31]. Oliveira et al.  evaluated such changes in subjects from 20 to over 60 years of age and showed that subjects over 40 yrs. had a significant decrement of suppression effect compared with those in their second and third decade. In our study we report a significant reduction in the presence (or detectability) of suppression with age. This is illustrated in Figure 2, in which we have included neonatal data from our previous study  where we reported a detection rate of contralateral DPOAE suppression (tested with the same methodology) of 95%. We propose that the age related degradation of contralateral OAE suppression starts from childhood, and is not confined to an elderly population. The corollary to the notion that there is a decline with age is to suppose that olivo-cochlear function is most important during early development. In that respect, a recent study reported that contralateral suppression of OAEs was significantly lower in children with receptive and expressive language delays compared with normal children . It is possible that the medial olivo-cochlear system is important in the development of normal sensory pathways and auditory learning [32, 33]. Our results suggest that the olivo-cochlear function, as revealed by contralateral suppression of DPOAEs, is very robust in a neonatal period but declines thereafter.
We note that our mean DPOAE suppression amplitude was relatively small (0.13 dB) compared to some other reports. For example Bassim et al.  reported the amplitude of DPOAE suppression by contralateral noise (in 20–30 year olds) to be 1.1 dB. In this case one major difference was the higher intensity (60 dB SPL) and longer duration (>4 s) of contralateral stimulus used compared to 0.5 s in the present study. We use this example to indicate the general difficulty in comparing across studies that use differing OAE measurement methods and stimulation protocols. In our study we find a general reduction in DPOAE suppression amplitude with age that is in agreement with a number of previous reports [17–21, 30, 31]. The cause of the suppression amplitude reduction can only be speculated on. There are the age-related cochlear changes that we discussed above in relation to OAEs, and in addition the degradation of more central auditory processes should be considered. These include inner haircell synaptic changes, de-myelination of neurons, and functional decline and decrement of cell number in cochlear nucleus [35–37]. Age-related synaptic loss of the MOC efferent innervations , the change of calcium regulatory proteins, and neurotransmitter acetylcholine (Ach)  have also been reported.
Age-related change in dynamics of DPOAE suppression
In addition to our own studies [14, 22, 23] on the dynamics of contralateral DPOAE suppression there have been a number of other reports [34, 40–43] however very few describe age-related changes. In mice, Sun and Kim reported that old animals tended to have a smaller adaptation magnitude and longer suppression time constants than younger mice, however they report no statistically significant changes in suppression onset latency .
In humans there is still much uncertainty about the actual latency of the olivo-cochlear reflex as revealed by contralateral OAE suppression. Mott et al. reported that contralateral stimulation changes spontaneous OAEs with latencies in the range of 40–200 ms (median = 120 ms); their methodology had a temporal resolution of 40 ms . Lind reported a 40–140 ms latency range for contralateral TEOAE suppression using a system with a 20 ms temporal resolution, respectively . In the present study we use a system with a temporal resolution that can be as low as 2 ms, and have previously reported a DPOAE suppression onset latency of 109 ms in young (20-30 yr) adults . In other reports much lower latencies have been reported. Thus, Maison et al. described a TEOAE suppression latency of less than 60 ms in 25–35 year old subjects . Backus and Guinan reported a very short latency of 25 ms (15-40 ms) for the medial olivo-cochlear reflex in young adults . Other studies have reported on various temporal aspects of the olivo-cochlear reflex [34, 42, 43], however, comparing these is difficult because of the various OAE recording methods, and protocols used.
It is useful perhaps to dissect out the timing at points along the pathway involved in contralateral suppression of DPOAE as follows: (i) stimulus transduction delay, from acoustic signal onset to the activation of inner hair cells; (ii) afferent neural transmission delay from the cochlea to (anteroventral) cochlear nucleus, to the superior olivary complex; (iii) inter-neuronal connection to cochlear efferent neurons; (iv) efferent neural delay from superior olive to OHCs via the crossed olivo-cochlear bundle; and (v) synaptic and mechanical activation times at OHC level including time for same to be manifest as DPOAE changes. The delay of step (i) is relatively small (<3 ms) and the timing of (ii) is similar to the latency of ABR wave PIII, approximately 6 ms. We will consider delay (iii) later. Regarding to the neural delay of (iv), Fex reported the efferent neural delay is 1.9-3.9 ms in the cat . Since, the length of efferent neurons in human is about 3 times those of cat, the delay of (iv) could be approximated to 10 ms in human. Konishi , and Kemp  and their colleagues observed (guinea pig) cochlear events (microphonics or OAEs) resulting from electrical stimulation of the crossed olivo-cochlear bundle and report a 10 ms delay which includes OHC post-synaptic events. This suggests that OHC post-synaptic delays are much longer than the cochlear efferent neural delays and that the total delay of step (v) in humans could be 30-50 ms. All of these timing values are, of course, approximations particularly when making extrapolations from animal models. However it is clear that delay (iii), an inter-neuronal processing within the superior olive, adds a significant time factor. There have been reports of age-related functional degradations in brainstem areas including the superior olive [49, 50] and we suggest that a significant part of the age related latency increase in DPOAE suppression onset originates at point (iii), the superior olive.
Regarding cochlear events, we report here that DPOAE suppression time constants did not show any significant age related changes (Figures 4 and 5). We interpret this as indicating that OHC mechanical events are not much affected by aging. However we are inclined to interpret our data with some caution. As can be noted in Figure 4, DPOAE suppression did not fully plateau with 0.5 s of contralateral stimulation, thus it is possible that we did not fully measure the overall time constants of DPOAE suppression. Other studies have been more analytical and describe DPOAE suppression or adaptation with a fast and a slow, two-exponent function [34, 43]; our data are consistent with time constants reported for the fast component of the suppression, but missing the slow component. Bassim et al. suggest that 10-20 s is required to characterize the slow component .
We report that DPOAE amplitude and DPOAE suppression by contralateral stimulation are degraded with aging, and some dynamic aspects of suppression are also changed with age. Our study was prompted by questions about the clinical utility of DPOAE suppression testing. We conclude that in neonates and young children, contralateral suppression of DPOAEs can be reliably measured, and can potentially inform us about the integrity of OHCs, of cochlear afferent and efferent function and also auditory brainstem mechanisms. We are particularly enthusiastic about our own real-time DPOAE measurement technique because it easily allows the DPOAE suppression dynamics (latency, time constants) to be quantified. We questioned whether such clinical testing was feasible in older subjects and find that the degree and detectability of DPOAE suppression falls off with age. For a clinical test to be widely applicable this may be considered a problem. On the other hand it may be revealing an important parameter of age related hearing loss that we have not been addressing previously.
Funding support for this project was from the Canadian Institutes of Health Research (CIHR).
- Kemp DT: Evidence of mechanical nonlinearity and frequency selective wave amplification in the cochlea. Arch Otorhinolaryngol. 1979, 224: 37-45.PubMedView ArticleGoogle Scholar
- Abdala C, Dhar S: Maturation and aging of the human cochlea: a view through the DPOAE looking glass. J Assoc Res Otolaryngol. 2012, 13: 403-421.PubMedPubMed CentralView ArticleGoogle Scholar
- McFadden SL, Campo P, Quaranta N, Henderson D: Age-related decline of auditory function in the chinchilla (Chinchilla laniger). Hear Res. 1997, 111: 114-126.PubMedView ArticleGoogle Scholar
- Dorn PA, Piskorski P, Keefe DH, Neely ST, Gorga MP: On the existence of an age/threshold/frequency interaction in distortion product otoacoustic emissions. J Acoust Soc Am. 1998, 104: 964-971.PubMedView ArticleGoogle Scholar
- Uchida Y, Ando F, Shimokata H, Sugiura S, Ueda H, Nakashima T: The effects of aging on distortion-product otoacoustic emissions in adults with normal hearing. Ear Hear. 2008, 29: 176-184.PubMedView ArticleGoogle Scholar
- Lonsbury-Martin BL, Cutler WM, Martin GK: Evidence for the influence of aging on distortion-product otoacoustic emissions in humans. J Acoust Soc Am. 1991, 89: 1749-1759.PubMedView ArticleGoogle Scholar
- Gates GA, Mills D, Nam BH, D’Agostino R, Rubel EW: Effects of age on the distortion product otoacoustic emission growth functions. Hear Res. 2002, 163: 53-60.PubMedView ArticleGoogle Scholar
- Kimberley BP, Hernadi I, Lee AM, Brown DK: Predicting pure tone thresholds in normal and hearing-impaired ears with distortion product emission and age. Ear Hear. 1994, 15: 199-209.PubMedView ArticleGoogle Scholar
- Rasmussen GL: The olivary peduncle and other fiber projections of the superior olivary complex. J Comp Neurol. 1946, 84: 141-220.PubMedView ArticleGoogle Scholar
- Guinan JJ: Olivocochlear efferents: anatomy, physiology, function, and the measurement of efferent effects in humans. Ear Hear. 2006, 27: 589-607.PubMedView ArticleGoogle Scholar
- Collet L, Kemp DT, Veuillet E, Duclaux R, Moulin A, Morgon A: Effect of contralateral auditory stimuli on active cochlear micromechanical properties in human subjects. Hear Res. 1990, 43: 251-261.PubMedView ArticleGoogle Scholar
- Puel JL, Rebillard G: Effect of contralateral sound stimulation on the distortion product 2f1-f2: evidence that the medial efferent system is involved. J Acoust Soc Am. 1990, 87: 1630-1635.PubMedView ArticleGoogle Scholar
- Walsh E, McGee J, McFadden S, Liberman M: Long-term effects of sectioning the olivocochlear bundle in neonatal cats. J Neurosci. 1998, 18: 3859-3869.PubMedGoogle Scholar
- James AL, Mount RJ, Harrison RV: Contralateral suppression of DPOAE measured in real time. Clin Otolaryngol. 2002, 27: 106-112.PubMedView ArticleGoogle Scholar
- Di Girolamo S, Napolitano B, Alessandrini M, Bruno E: Experimental and clinical aspects of the efferent auditory system. Acta Neurochir Suppl. 2007, 97: 419-424.PubMedView ArticleGoogle Scholar
- James AL: The assessment of olivocochlear function in neonates with real-time distortion product otoacoustic emissions. Laryngoscope. 2011, 121: 202-213.PubMedView ArticleGoogle Scholar
- Sun X-M, Kim DO: Adaptation of 2f1– 2f2 distortion product otoacoustic emission in young-adult and old CBA and C57 mice. J Acoust Soc Am. 1999, 105: 3399-3409.PubMedView ArticleGoogle Scholar
- Varghese GI, Zhu X, Frisina RD: Age-related declines in distortion product otoacoustic emissions utilizing pure tone contralateral stimulation in CBA/CaJ mice. Hear Res. 2005, 209: 60-67.PubMedView ArticleGoogle Scholar
- Zhu X, Vasilyeva ON, Kim S, Jacobson M, Romney J, Waterman MS, Tuttle D, Frisina RD: Auditory efferent feedback system deficits precede age-related hearing loss: contralateral suppression of otoacoustic emissions in mice. J Comp Neurol. 2007, 503: 593-604.PubMedView ArticleGoogle Scholar
- Jacobson M, Kim S, Romney J, Zhu X, Frisina RD: Contralateral suppression of distortion-product otoacoustic emissions declines with age: a comparison of findings in CBA mice with human listeners. Laryngoscope. 2003, 113: 1707-1713.PubMedView ArticleGoogle Scholar
- Kim S, Frisina DR, Frisina RD: Effects of age on contralateral suppression of distortion product otoacoustic emissions in human listeners with normal hearing. Audiol Neurootol. 2002, 7: 348-357.PubMedView ArticleGoogle Scholar
- Harrison RV, Sharma A, Brown T, Jiwani S, James AL: Amplitude modulation of DPOAEs by acoustic stimulation of the contralateral ear. Acta Otolaryngol. 2008, 128: 404-407.PubMedView ArticleGoogle Scholar
- James AL, Harrison RV, Pienkowski M, Dajani HR, Mount RJ: Dynamics of real time DPOAE contralateral suppression in chinchillas and humans. Int J Audiol. 2005, 44: 118-129.PubMedView ArticleGoogle Scholar
- Williams DM, Brown AM: The effect of contralateral broad-band noise on acoustic distortion products from the human ear. Hear Res. 1997, 104: 127-146.PubMedView ArticleGoogle Scholar
- Collet L, Veuillet E, Berger-Vachon C, Morgon A: Evoked otoacoustic emissions: relative importance of age, sex and sensorineural hearing-loss using a mathematical model of the audiogram. Int J Neurosci. 1992, 62: 113-122.PubMedView ArticleGoogle Scholar
- Kuroda T: Clinical investigation on spontaneous otoacoustic emission (SOAE) in 447 ears. Auris Nasus Larynx. 2007, 34: 29-38.PubMedView ArticleGoogle Scholar
- Ohlemiller KK: Age-related hearing loss: the status of Schuknecht’s typology. Curr Opin Otolaryngol Head Neck Surg. 2004, 12: 439-443.PubMedView ArticleGoogle Scholar
- Lang H, Jyothi V, Smythe NM, Dubno JR, Schulte BA, Schmiedt RA: Chronic reduction of endocochlear potential reduces auditory nerve activity: further confirmation of an animal model of metabolic presbyacusis. J Assoc Res Otolaryngol. 2010, 11: 419-434.PubMedPubMed CentralView ArticleGoogle Scholar
- Bohne BA, Gruner MM, Harding GW: Morphological correlates of aging in the chinchilla cochlea. Hear Res. 1990, 48: 79-91.PubMedView ArticleGoogle Scholar
- Keppler H, Dhooge I, Corthals P, Maes L, D’haenens W, Bockstael A, Philips B, Swinnen F, Vinck B: The effects of aging on evoked otoacoustic emissions and efferent suppression of transient evoked otoacoustic emissions. Clin Neurophysiol. 2010, 121: 359-365.PubMedView ArticleGoogle Scholar
- Oliveira JR, Fernandes JC, Costa Filho OA: Age impact on the efferent system activities in cochlear mechanical properties in normal hearing individuals. Braz J Otorhinolaryngol. 2009, 75: 340-344.PubMedView ArticleGoogle Scholar
- Yalçinkaya F, Yilmaz ST, Muluk NB: Transient evoked otoacoustic emissions and contralateral suppressions in children with auditory listening problems. Auris Nasus Larynx. 2010, 37: 47-54.PubMedView ArticleGoogle Scholar
- de Boer J, Thornton AR: Neural correlates of perceptual learning in the auditory brainstem: efferent activity predicts and reflects improvement at a speech-in-noise discrimination task. J Neurosci. 2008, 28: 4929-4937.PubMedView ArticleGoogle Scholar
- Bassim MK, Miller RL, Buss E, Smith DW: Rapid adaptation of the 2f1-f2 DPOAE in humans: binaural and contralateral stimulation effects. Hear Res. 2003, 182: 140-152.PubMedView ArticleGoogle Scholar
- Frisina DR, Frisina RD: Speech recognition in noise and presbycusis: relations to possible neural sites. Hear Res. 1997, 106: 95-104.PubMedView ArticleGoogle Scholar
- Walton JP, Frisina RD, O’Neill WE: Age-related alterations in neural processing of silent gaps in the central nucleus of the inferior colliculus in the CBA mouse model of presbycusis. J Neurosci. 1998, 18: 2764-2776.PubMedGoogle Scholar
- Harkrider AW, Bowers CD: Evidence for a cortically mediated release from inhibition in the human cochlea. J Am Acad Audiol. 2009, 20: 208-215.PubMedView ArticleGoogle Scholar
- Fu B, Le Prell C, Simmons D, Lei D, Schrader A, Chen AB, Bao J: Age-related synaptic loss of the medial olivocochlear efferent innervation. Mol Neurodegener. 2010, 5: 53.PubMedPubMed CentralView ArticleGoogle Scholar
- Lynch-Erhardt MA, Frisina RD: Presence of acetyl cholinesterase labeling in the auditory brainstem of young adult and old CEA mice. Assoc Res Oto laryngol Abstr. 2001, 24: 282.Google Scholar
- Maison S, Durrant J, Gallineau C, Micheyl C, Collet L: Delay and temporal integration in medial olivocochlear bundle activation in humans. Ear Hear. 2001, 22: 65-74.PubMedView ArticleGoogle Scholar
- Backus BC, Guinan JJ: Time-course of the human medial olivocochlear reflex. J Acoust Soc Am. 2006, 119: 2889-2904.PubMedView ArticleGoogle Scholar
- Hill JC, Prasher DK, Luxon LM: Latency of contralateral sound-evoked auditory efferent suppression of otoacoustic emissions. Acta Otolaryngol. 1997, 117: 343-351.PubMedView ArticleGoogle Scholar
- Kim DO, Dorn PA, Neely ST, Gorga MP: Adaptation of distortion product otoacoustic emission in humans. J Assoc Res Otolaryngol. 2001, 2: 31-40.PubMedPubMed CentralView ArticleGoogle Scholar
- Mott JB, Norton SJ, Neely ST, Warr WB: Changes in spontaneous otoacoustic emissions produced by acoustic stimulation of the contralateral ear. Hear Res. 1989, 38: 229-242.PubMedView ArticleGoogle Scholar
- Lind O: Contralateral suppression of TEOAE. Attempts to find a latency. Br J Audiol. 1994, 28: 219-225.PubMedView ArticleGoogle Scholar
- Fex J: Neuropharmacology and potentials of the inner ear. Basic Mechanisms in Hearing. Edited by: Moller AR. 1973, New York: Academic Press, 377-420.View ArticleGoogle Scholar
- Konishi T, Slepian JZ: Effects of the electrical stimulation of the crossed olivocochlear bundle on cochlear potentials recorded with intracochlear electrodes in guinea pigs. J Acoust Soc Am. 1971, 49: 1762-1769.PubMedView ArticleGoogle Scholar
- Kemp DT, Souter M: A new rapid component in the cochlear response to brief electrical efferent stimulation: CM and otoacoustic observations. Hear Res. 1988, 34: 49-62.PubMedView ArticleGoogle Scholar
- Reuss S, Schaeffer DF, Laages MH, Riemann R: Evidence for increased nitric oxide production in the auditory brain stem of the aged dwarf hamster (Phodopus sungorus): an NADPH-diaphorase histochemical study. Mech Ageing Dev. 2000, 112: 125-134.PubMedView ArticleGoogle Scholar
- Caspary DM, Ling L, Turner JG, Hughes LF: Inhibitory neurotransmission, plasticity and aging in the mammalian central auditory system. J Exp Biol. 2008, 211: 1781-1791.PubMedPubMed CentralView ArticleGoogle Scholar
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