Level dependence of distortion product otoacoustic emissions in the leopard frog, Rana pipiens pipiens

Hearing Research

Volumn 192, Issue 1-2, 2004, Pages 107-118

  Meenderink, Sebastiaan W F ^a   Van Dijk, Pim ^a  

^a NONE

Author keywords

AP, amphibian papilla; AP DPOAE, distortion product otoacoustic emission from the amphibian papilla; BP, basilar papilla; DPOAE, distortion product otoacoustic emission; I O curve, input output curve

Indexed keywords

ANIMAL EXPERIMENT; ARTICLE; AUDITORY CORTEX; AUDITORY DISCRIMINATION; AUDITORY LATERALIZATION; AUDITORY THRESHOLD; BASILAR MEMBRANE; CONTROLLED STUDY; DISTORTION PRODUCT OTOACOUSTIC EMISSION; INNER EAR; LOW FREQUENCY NOISE; NONHUMAN; PRIORITY JOURNAL; SOUND TRANSMISSION;

ACOUSTIC STIMULATION; ANIMALS; BIOMETRY; MODELS, BIOLOGICAL; OTOACOUSTIC EMISSIONS, SPONTANEOUS; RANA PIPIENS;

EID: 2442427373     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.heares.2004.01.015     Document Type: Article

References (47)

1. 2) amplitude growth in human adults and neonates J. Acoust. Soc. Am. 107:2000;446-456
2. Brown A.M. Acoustic distortion from rodent ears: a comparison of responses from rats, guinea pigs, and gerbils. Hear. Res. 31:1987;25-38
3. Brownell W.E., Bader C.R., Bertrand D., de Ribaupierre Y. Evoked mechanical responses of isolated cochlear outer hair cells. Science. 227:1985;194-196
4. 2 distortion-product otoacoustic emission in a moth Hear. Res. 162:2001;126-133
5. Crawford A.C., Fettiplace R. The mechanical properties of ciliary bundles of turtle cochlear hair cells. J. Physiol. 364:1985;359-379
6. Dorn P.A., Konrad-Martin D., Neely S.T., Keefe D.H., Cyr E., Gorga M.P. Distortion product otoacoustic emission input/output functions in normal-hearing and hearing-impaired human ears. J. Acoust. Soc. Am. 110:2001;3119-3131
7. Dreisbach L.E., Siegel J.H. Distortion-product otoacoustic emissions measured at high frequencies in humans. J. Acoust. Soc. Am. 110:2001;2456-2469
8. Feng A.S., Narins P.M., Capranica R.R. Three populations of primary auditory nerve fibers in the bullfrog (Rana catesbeiana): their peripheral origins and frequency sensitivities. J. Comp. Physiol. 100:1975;221-229
9. Frishkopf L.S., Flock A. Ultrastructure of the basilar papilla, an auditory organ in the bullfrog. Acta Otolaryngol. 77:1974;176-184
10. Frishkopf L.S., Goldstein M.H. Responses to acoustic stimuli from single units in the eigth nerve of the bullfrog. J. Acoust. Soc. Am. 35:1963;1219-1228
11. Frishkopf L.S., Capranica R.R., Goldstein M.H. Neural coding in the bullfrog's auditory system - a teleological approach. Proc. IEEE. 56:1968;969-980
12. Froymovich O., Rebala V., Salvi R.J., Rassael H. Long-term effect of acoustic trauma on distortion product otoacoustic emissions in chickens. J. Acoust. Soc. Am. 97:1995;3021-3029
13. 2, from the human ear and its relation to auditory sensitivity J. Acoust. Soc. Am. 88:1990;821-839
14. He D.Z., Beisel K.W., Chen L., Ding D.L., Jia S., Fritzsch B., Salvi R. Chick hair cells do not exhibit voltage-dependent somatic motility. J. Physiol. 546:2003;511-520
15. Hillery C.M., Narins P.M. Neurophysiological evidence for a traveling wave in the amphibian inner ear. Science. 225:1984;1037-1039
16. Howard J., Hudspeth A.J. Compliance of the hair bundle associated with gating of mechanoelectrical transduction channels in the bullfrog's saccular hair cell. Neuron. 1:1988;189-199
17. Hudspeth A. Mechanical amplification of stimuli by hair cells. Curr. Opin. Neurobiol. 7:1997;480-486
18. Kemp D.T. Evidence of mechanical nonlinearity and frequency selective wave amplification in the cochlea. Arch. Otorhinolaryngol. 224:1979;37-45
19. Kennedy H.J., Evans M.G., Crawford A.C., Fettiplace R. Fast adaptation of mechanoelectrical transducer channels in mammalian cochlear hair cells. Nature Neurosci. 6:2003;832-836
20. Kettembeil S., Manley G.A., Siegl E. Distortion-product otoacoustic emissions and their anesthesia sensitivity in the European Starling and the chicken. Hear. Res. 86:1995;47-62
21. Kim D.O. Cochlear mechanics: implications of electrophysiological and acoustical observations. Hear. Res. 2:1980;297-317
22. Lewis, E.R., 1978. Comparative studies of the anuran auditory papillae. Scanning Electron Microscopy II, pp. 633-642
23. Lewis E.R., Leverenz E.L., Koyama H. The tonotopic organization of the bullfrog amphibian papilla, an auditory organ lacking a basilar membrane. J. Comp. Physiol. 145:1982;437-445
24. Liberman M.C., Gao J., He D.Z.Z., Wu X., Jia S., Zuo J. Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier. Nature. 419:2002;300-304
25. Lonsbury-Martin B.L., Harris F.P., Stagner B.B., Hawkins M.D., Martin G.K. Distortion product emissions in humans. I. Basic properties in normally hearing subjects. Ann. Otol. Rhinol. Laryngol. Suppl. 147:1990;3-14
26. Lonsbury-Martin B.L., Martin G.K., Probst R., Coats A.C. Acoustic distortion products in rabbit ear canal. I. Basic features and physiological vulnerability. Hear. Res. 28:1987;173-189
27. Lukashkin A.N., Russell I.J. A descriptive model of the receptor potential nonlinearities generated by the hair cell mechanoelectrical transducer. J. Acoust. Soc. Am. 103:1998;973-980
28. 2 distortion components generated by the hair cell mechanoelectrical transducer: dependence on the amplitudes of the primaries and feedback gain J. Acoust. Soc. Am. 106:1999;2661-2668
29. Manley G. Otoacoustic emissions in lizards. Manley G.A., Fastl H., Kössl M., Oeckinghaus H., Klump G.M. Auditory Worlds: Sensory Analysis and Perception in Animals and Man. 2000;93-102 Wiley-VCH, Weinheim
30. Manley G.A. Evidence for an active process and a cochlear amplifier in nonmammals. J. Neurophysiol. 86:2001;541-549
31. Manley G.A. Evolution of structure and function of the hearing organ in lizards. J. Neurobiol. 53:2002;202-211
32. Manley G.A., Köppl C., Johnstone B.M. Distortion-product otoacoustic emissions in the bobtail lizard. I. General characteristics. J. Acoust. Soc. Am. 93:1993;2820-2833
33. Mills D.A. Interpretation of distortion product otoacoustic emission measurements. I. Two stimulus tones. J. Acoust. Soc. Am. 102:1997;413-429
34. Mills D.M., Rubel E.W. Development of the cochlear amplifier. J. Acoust. Soc. Am. 100:1996;428-441
35. Mills D.M., Norton S.J., Rubel E.W. Vulnerability and adaptation of distortion product otoacoustic emissions to endocochlear potential variation. J. Acoust. Soc. Am. 94:1993;2108-2122
36. Ronken D.A. Spike discharge properties that are related to the characteristic frequency of single units in the frog auditory nerve. J. Acoust. Soc. Am. 90:1991;2428-2440
37. Rosowski J.J., Peake W.T., White J.R. Cochlear nonlinearities from two-tone distortion products in the ear canal of the alligator lizard. Hear. Res. 13:1984;141-158
38. Smotherman M.S., Narins P.M. The electrical properties of auditory hair cells in the frog amphibian papilla. J. Neurosci. 19:1999;5275-5292
39. Sun H., Salvi R.J., Ding D.L., Hashino E., Shero M., Zheng X.Y. Excitotoxic effect of kainic acid on chicken otoacoustic emissions and cochlear potentials. J. Acoust. Soc. Am. 107:2000;2136-2142
40. Talmadge C.L., Tubis A., Long G.R., Piskorski P. Modeling otoacoustic emission and hearing treshold fine structures. J. Acoust. Soc. Am. 104:1998;1517-1543
41. 2 in the barn owl Hear. Res. 123:1998;183-200
42. Van Dijk P., Manley G.A. Distortion product otoacoustic emissions in the tree frog Hyla cinerea. Hear. Res. 153:2001;14-22
43. Van Dijk P., Mason M.J., Narins P.M. Distortion product otoacoustic emissions in frogs: correlation with middle and inner ear properties. Hear. Res. 173:2002;100-108
44. Van Dijk P., Narins P.M., Mason M.J. Physiological vulnerability of distortion product otoacoustic emissions from the amphibian ear. J. Acoust. Soc. Am. 114:2003;2044-2048
45. 2 distortion-product otoacoustic emission in rabbit. I. Differential dependence on stimulus parameters J. Acoust. Soc. Am. 91:1992;1587-1607
46. Zheng J., Shen W., He D.Z., Long K.B., Dallos P. Prestin is the motor protein of cochlear outer hair cells. Nature. 405:2000;149-155
47. Zurek P.M., Clark W., Kim D.O. The behavior of acoustic distortion products in the ear canals of chinchillas with normal or damaged ears. J. Acoust. Soc. Am. 72:1982;774-780