Caffeine and ryanodine demonstrate a role for the ryanodine receptor in the organ of Corti

Hearing Research

Volumn 174, Issue 1-2, 2002, Pages 172-182

  Bobbin, Richard P ^a  

^a LOUISIANA STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Action potential; Cochlear microphonic; Distortion product; Summating potential

Indexed keywords

CAFFEINE; CALCIUM ION; RYANODINE; RYANODINE RECEPTOR; SALICYLIC ACID; SALICYLIC ACID DERIVATIVE;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CALCIUM TRANSPORT; COCHLEA FENESTRA; COCHLEA POTENTIAL; COCHLEAR NERVE; CONCENTRATION RESPONSE; CONTROLLED STUDY; CORTI ORGAN; DISTORTION PRODUCT OTOACOUSTIC EMISSION; DRUG EFFECT; FEMALE; HAIR CELL; LATENT PERIOD; MALE; NERVE POTENTIAL; NONHUMAN; PERILYMPH; PRIORITY JOURNAL; SOUND INTENSITY; ACTION POTENTIAL; ANIMAL; COCHLEA; ELECTROSTIMULATION; GUINEA PIG; PERCEPTION DISORDER; PHYSIOLOGY; SPONTANEOUS OTOACOUSTIC EMISSION;

ACTION POTENTIALS; ANIMALS; CAFFEINE; COCHLEA; COCHLEAR MICROPHONIC POTENTIALS; ELECTRIC STIMULATION; FEMALE; GUINEA PIGS; MALE; ORGAN OF CORTI; OTOACOUSTIC EMISSIONS, SPONTANEOUS; PERCEPTUAL DISTORTION; RYANODINE; RYANODINE RECEPTOR CALCIUM RELEASE CHANNEL; SALICYLATES;

EID: 0036888728     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-5955(02)00654-8     Document Type: Article

References (45)

1. Ashmore J.F., Ohmori H. Control of intracellular calcium by ATP in isolated outer hair cells of the guinea-pig cochlea. J. Physiol. 428:1990;109-131.
2. Berridge M.J. Neuronal calcium signaling. Neuron. 21:1998;13-26.
3. Bledsoe S.C. Jr., Bobbin R.P., Chihal D.M. Kainic acid: an evaluation of its action on cochlear potentials. Hear. Res. 4:1981;109-120.
4. Bobbin R.P. ATP induced motion of the stalks of isolated cochlear Deiters' cells. NeuroReport. 12:2001;1000-1004.
5. Bobbin, R.P., Kisiel, D.L., 1981. Physiology of hearing. In: Brown, R.D., Daigneault, E.A. (Eds.), Pharmacology of Hearing. John Wiley and Sons, New York, pp. 19-50.
6. Bobbin, R.P., Campbell, J., Lousteau, S., Mandhare, M., 2002. Electrical and ATP induced movements of the phalangeal processes of isolated cochlear Deiters' cells. In: Berlin, C.I., Hood, L., Ricci, A. (Eds.), Inner Ear Biology: Basic Science and Clinical Applications. Singular Publishing Group, San Diego, CA, pp. 91-106.
7. Bobbin R.P., Fallon M., Kujawa S.G. Magnitude of the negative summating potential varies with perilymph calcium levels. Hear. Res. 56:1991;101-110.
8. Bobbin, R.P., LeBlanc, Mandhare, M., Parker, M.S., 2001. Additional studies on the role of ATP as a neuromodulator in the organ of Corti. In: Berlin, C.I., Bobbin, R.P. (Eds.), Hair Cells: Micromechanics and Hearing. Singular Publishing Group, San Diego, CA, pp. 129-153.
9. Chen C., Bobbin R.P. P2X receptors in cochlear Deiters' cells. Br. J. Pharmacol. 124:1998;337-344.
10. Chen C., Skellett R.A., Fallon M., Bobbin R.P. Additional pharmacological evidence that endogenous ATP modulates cochlear mechanics. Hear. Res. 118:1998;47-61.
11. Chung J.W., Schacht J. ATP and nitric oxide modulate intracellular calcium in isolated pillar cells of the guinea pig cochlea. J. Assoc. Res. Otolaryngol. 4:2001;399-407.
12. Dallos P., He D.Z.Z., Lin X., Sziklai I., Mehta S., Evans B.N. Acetylcholine, outer hair cell electromotility, and the cochlear amplifier. J. Neurosci. 17:1997;2212-2226.
13. 2+ evokes reversible mechanical responses in supporting cells of the guinea-pig organ of Corti. Biochem. Biophys. Res. Commun. 201:1994;1263-1269.
14. Fitzgerald J.J., Robertson D., Johnstone B.M. Effects of intra-cochlear perfusion of salicylates on cochlear microphonic and other auditory responses in the guinea pig. Hear. Res. 67:1993;147-156.
15. Haak L.L., Song L.-S., Molinski T.F., Pessah I.N., Cheng H., Russell J.T. Sparks and puffs in oligodendrocyte progenitors: cross talk between ryanodine receptors and inositol trisphosphate receptors. J. Neurosci. 21:2001;3860-3870.
16. Konishi T., Slepian J. Summating potential with electrical stimulation of crossed olivocochlear bundles. Science. 172:1971;483-484.
17. Kujawa S.G., Erostegui C., Fallon M., Crist J., Bobbin R.P. Effects of adenosine 5′-triphosphate and related agonists on cochlear function. Hear. Res. 76:1994;87-100.
18. Kujawa S.G., Fallon M., Bobbin R.P. Intracochlear salicylate reduces low intensity acoustic and cochlear microphonic distortion products. Hear. Res. 64:1992;73-80.
19. 1 DPOAE response to continuous primary stimulation. II. Influence of local calcium-dependent mechanisms. Hear. Res. 97:1996;153-164.
20. Lagostena L., Mammano F. Intracellular calcium dynamics and membrane conductance changes evoked by Deiters' cell purinoceptor activation in the organ of Corti. Cell Calcium. 29:2001;191-196.
21. Lagostena L., Ashmore J.F., Kachar B., Mammano F. Purinergic control of intercellular communication between Hensen's cells of the guinea-pig cochlea. J. Physiol. 531:2001;693-706.
22. 2+ store to the base of the sensory hair bundle. J. Neurosci. 19:1999;6918-6929.
23. Matsunobu T., Schacht J. Nitric oxide/cyclic GMP pathway attenuates ATP-evoked intracellular calcium increase in supporting cells of the guinea pig cochlea. J. Comp. Neurol. 423:2000;452-461.
24. Murugasu E., Russell I.J. Salicylate ototoxicity: the effects on basilar membrane displacement, cochlear microphonics, and neural responses in the basal turn of the guinea pig cochlea. Aud. Neurosci. 1:1995;139-150.
25. Murugasu E., Russell I.J. The role of calcium on the effects of intracochlear acetylcholine perfusion on basilar membrane displacement in the basal turn of the guinea pig cochlea. Aud. Neurosci. 2:1996;363-376.
26. + channel. Hear. Res. 101:1996;149-172.
27. Patuzzi R.B., Yates G.K., Johnstone B.M. The origin of the low-frequency microphonic in the first cochlear turn of the guinea pig. Hear. Res. 39:1989;177-188.
28. Puel J.-L., Bledsoe S.C. Jr., Bobbin R.P., Ceasar G., Fallon M. Comparative actions of salicylate on the amphibian lateral line and the guinea pig cochlea. Comp. Biochem. Physiol. 93C:1989;73-80.
29. Puel J.-L., Bobbin R.P., Fallon M. The active process is affected first by intense sound exposure. Hear. Res. 37:1988;53-64.
30. Ricci, A.J., 2001. Fast transducer adaptation, physiological implications and underlying mechanisms. In: Berlin, C.I., Bobbin, R.P. (Eds.), Hair Cells: Micromechanics and Hearing. Singular Publishing Group, San Diego, CA, pp. 45-66.
31. Robles L., Ruggero M.A. Mechanics of the mammalian cochlea. Physiol. Rev. 81:2001;1305-1352.
32. Ruel J., Bobbin R.P., Vidal D., Pujol R., Puel J.L. The selective AMPA receptor antagonist GYKI53784 blocks action potential generation and excitotoxicity in the guinea pig cochlea. Neuropharmacology. 39:2000;1959-1973.
33. Ruel J., Chen C., Caicedo A., Pujol R., Bobbin R.P., Puel J.L. AMPA-preferring glutamate receptors in cochlear physiology of adult guinea pig. J. Physiol. 518.3:1999;667-680.
34. Santos-Sacchi, J., 2001. Cochlear Physiology. In: Jahn, A.F., Santos-Sacchi, J. (Eds.), Physiology of the Ear. Singular Publishing Group, San Diego, CA, pp. 357-392.
35. Sato Y., Handa T., Matsumura M., Orita Y. Gap junction change in supporting cells of the organ of Corti with ryanodine and caffeine. Acta Otolaryngol. 118:1998;821-825.
36. Skellett R.A., Crist J.R., Fallon M., Bobbin R.P. Caffeine-induced shortening of isolated outer hair cells: an osmotic mechanism of action. Hear. Res. 87:1995;41-48.
37. Skellett R.A., Chen C., Fallon M., Nenov A.P., Bobbin R.P. Pharmacological evidence that endogenous ATP modulates cochlear mechanics. Hear. Res. 111:1997;42-54.
38. Sridhar T.S., Brown M.C., Sewell W.F. Unique postsynaptic signaling at the hair cell efferent synapse permits calcium to evoke changes on two time scales. J. Neurosci. 17:1997;428-437.
39. Sugasawa M., Erostegui C., Blanchet C., Dulon D. ATP activates non-selective cationic channels and calcium release in inner hair cells of the guinea-pig cochlea. J. Physiol. 491:1996;707-718.
40. Sziklai I., Szonyi M., Dallos P. Phosphorylation mediates the influence of acetylcholine upon outer hair cell electromotility. Acta Otolaryngol. 121:2001;153-156.
41. Take K. Effects of thapsigargin and ryanodine on cochlear electrical potentials in guinea pigs examined by the perilymphatic perfusion method. Nippon Jibiinkoka Gakkai Kaiho. 99:1996;1641-1647.
42. Yamamoto T., Kakehata S., Yamada T., Saito T., Saito H., Akaike N. Caffeine rapidly decreases potassium conductance of dissociated outer hair cells of guinea-pig cochlea. Brain Res. 677:1995;89-96.
43. 2+ channels in transmitter release from mammalian inner hair cells. I. Gross sound-evoked potentials. J. Neurophysiol. 82:1999;3307-3315.
44. Zheng J., Shen W., He D., Long K., Madison L.D., Dallos P. Prestin is the motor protein of cochlear outer hair cells. Nature. 405:2000;149-155.
45. 2+ channel/ryanodine receptor: modulation by endogenous effectors, drugs and disease states. Pharm. Rev. 49:1997;1-51.