期刊论文详细信息
Journal of Otolaryngology-Head & Neck Surgery
Age related changes to the dynamics of contralateral DPOAE suppression in human subjects
Robert V Harrison3  Adrian L James3  Sohit Kanotra2  Ujimoto Konomi1 
[1] Department of Otolaryngology, Tokyo Medical University, 6-7-1, Nishishinjuku, Shinjuku-ku, Tokyo 160-0023, Japan;Auditory Science Laboratory, Department of Otolaryngology-Head and Neck Surgery, The Hospital for Sick Children, 555 University Ave, Toronto, Ontario M5G 1X8, Canada;Department of Otolaryngology-Head and Neck Surgery, University of Toronto, 190 Elizabeth St., Rm 3S-438, R. Fraser Elliott Building, Toronto, Ontario M5G 2 N2, Canada
关键词: Otoacoustic emissions;    Age-related hearing loss;    Aging;    Cochlear inhibition;    Olivo-cochlear efferents;    Superior olivary complex;    Outer haircells;   
Others  :  861354
DOI  :  10.1186/1916-0216-43-15
 received in 2014-01-27, accepted in 2014-06-11,  发布年份 2014
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【 摘 要 】

Background

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.

Methods

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.

Results

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.

Conclusion

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.

【 授权许可】

   
2014 Konomi et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Kemp DT: Evidence of mechanical nonlinearity and frequency selective wave amplification in the cochlea. Arch Otorhinolaryngol 1979, 224:37-45.
  • [2]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.
  • [3]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.
  • [4]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.
  • [5]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.
  • [6]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.
  • [7]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.
  • [8]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.
  • [9]Rasmussen GL: The olivary peduncle and other fiber projections of the superior olivary complex. J Comp Neurol 1946, 84:141-220.
  • [10]Guinan JJ Jr: Olivocochlear efferents: anatomy, physiology, function, and the measurement of efferent effects in humans. Ear Hear 2006, 27:589-607.
  • [11]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.
  • [12]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.
  • [13]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.
  • [14]James AL, Mount RJ, Harrison RV: Contralateral suppression of DPOAE measured in real time. Clin Otolaryngol 2002, 27:106-112.
  • [15]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.
  • [16]James AL: The assessment of olivocochlear function in neonates with real-time distortion product otoacoustic emissions. Laryngoscope 2011, 121:202-213.
  • [17]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.
  • [18]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.
  • [19]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.
  • [20]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.
  • [21]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.
  • [22]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.
  • [23]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.
  • [24]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.
  • [25]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.
  • [26]Kuroda T: Clinical investigation on spontaneous otoacoustic emission (SOAE) in 447 ears. Auris Nasus Larynx 2007, 34:29-38.
  • [27]Ohlemiller KK: Age-related hearing loss: the status of Schuknecht’s typology. Curr Opin Otolaryngol Head Neck Surg 2004, 12:439-443.
  • [28]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.
  • [29]Bohne BA, Gruner MM, Harding GW: Morphological correlates of aging in the chinchilla cochlea. Hear Res 1990, 48:79-91.
  • [30]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.
  • [31]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.
  • [32]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.
  • [33]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.
  • [34]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.
  • [35]Frisina DR, Frisina RD: Speech recognition in noise and presbycusis: relations to possible neural sites. Hear Res 1997, 106:95-104.
  • [36]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.
  • [37]Harkrider AW, Bowers CD: Evidence for a cortically mediated release from inhibition in the human cochlea. J Am Acad Audiol 2009, 20:208-215.
  • [38]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.
  • [39]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.
  • [40]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.
  • [41]Backus BC, Guinan JJ Jr: Time-course of the human medial olivocochlear reflex. J Acoust Soc Am 2006, 119:2889-2904.
  • [42]Hill JC, Prasher DK, Luxon LM: Latency of contralateral sound-evoked auditory efferent suppression of otoacoustic emissions. Acta Otolaryngol 1997, 117:343-351.
  • [43]Kim DO, Dorn PA, Neely ST, Gorga MP: Adaptation of distortion product otoacoustic emission in humans. J Assoc Res Otolaryngol 2001, 2:31-40.
  • [44]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.
  • [45]Lind O: Contralateral suppression of TEOAE. Attempts to find a latency. Br J Audiol 1994, 28:219-225.
  • [46]Fex J: Neuropharmacology and potentials of the inner ear. In Basic Mechanisms in Hearing. Edited by Moller AR. New York: Academic Press; 1973:377-420.
  • [47]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.
  • [48]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.
  • [49]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.
  • [50]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.
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