Comparative Ototoxicity of Four Aminoglycosidic Antibiotics during the Critical Period of Cochlear Development in the Rat

References

• Alford B. R., Ruben R. J. Physiological, behavioral and anatomical correlates on the development of hearing in the mouse. Ann Otol Rhinol Laryngol 1963; 72: 237
   PubMed Web of Science ®Google Scholar
• Aran J. M. Electrophysiology of cochlear toxicity. Aminoglycoside Ototoxicity, S. A. Lerner, G. J. Matz, J. E. Hawkins. Little, Brown & Co., Boston 1981; 31–47
   Google Scholar
• Aran J. M., Cazals Y. Electrocochleography: Animals studies. Evoked Electrical Activity in the Auditory Nervous System, R. F. Naunton, C. Fernandez. Academic Press, New York 1978; 239–57
   Google Scholar
• Aran J. M., Erre J. P., Guilhaume A., Aurousseau C. The comparative ototoxicities of gentamicin, tobramycin and dibekacin in the guinea pig. A functional and morphological cochlear and vestibular Study. Acta Otolaryngol 1982, Suppl. 390
   PubMedGoogle Scholar
• Bernard P. Freedom from ototoxicity in aminoglycoside‐treated neonates: a mistaken notion. Laryngoscope 1981; 91: 1985
   PubMed Web of Science ®Google Scholar
• Bernard P., Pechere J. C., Hebert R. Altered objective audiometry in aminoglycosides‐treated human neonates. Arch Otorhinolaryngol 1980; 228: 205
   PubMed Web of Science ®Google Scholar
• Bredberg G., Ades H. W., Engström H. Scanning electron microscopy of the normal and pathologically altered organ of Corti. In Inner Ear Studies. Acta Otolaryngol 1972; 301: 3–48, Suppl.
   Google Scholar
• Brummett R. E., Fox K. E., Beudrick T. W., Himes D. L. Ototoxicity of tobramycin, gentamicin, amikacin and sisomicin in the guinea‐pig. J Antimicrob Chemother 1978; 4: 73
   PubMed Web of Science ®Google Scholar
• Carlier E., Lenoir M., Pujol R. Development of cochlear frequency selectivity tested by compound action potential tuning curves. Hearing Res 1979; 1: 197
   Web of Science ®Google Scholar
• Carlier E., Pujol R. Supra‐normal sensitivity to ototoxic antibiotic of the developing rat cochlea. Arch Otorhinolaryngol 1980; 226: 129
   PubMedGoogle Scholar
• Crawley D. E., Hepp‐Raymond M. C. Development of cochlear function in the infant rat. J Comp Physiol Psychol 1966; 62: 427
   Web of Science ®Google Scholar
• Dallos P., Cheatham M. E. Production of cochlear potentials by inner and outer hair cells. J Acoust Soc Am 1976; 60: 510
   PubMed Web of Science ®Google Scholar
• Darrouzet J., Guilhaume A. Ototoxicité cochléaire comparée de trois antibiotiques; kanamycine, gentamicine, tobramycine. Etude histologique et ultrastructurale. Rev Laryngol Otol Rhinol 1976; 97: 655
   PubMedGoogle Scholar
• Dumas G., Charachon R. Ototoxicity of kanamycin in developing guinea‐pigs. Acta Otolaryngol (Stockh) 1982; 94: 203
   PubMed Web of Science ®Google Scholar
• Hawkins J. E., Lurie M. H. Ototoxicity of streptomycin. Ann Otol Rhinol Laryngol 1952; 61: 789
   PubMed Web of Science ®Google Scholar
• Hawkins J. E., Jr, Johnsson L. G., Aran J. N. Comparative tests of gentamicin ototoxicity. J Infect Dis 1969; 119: 417
   PubMed Web of Science ®Google Scholar
• Hawkins J. E., Jr, Johnsson L. G. Histopathology of cochlear and vestibular ototoxicity in laboratory animals. Aminoglycoside Ototoxicity, S. A. Lerner, G. J. Matz, J. E. Hawkins. Little, Brown & Co., Boston 1981; 31–47
   Google Scholar
• Henry K. R., Chole R. A., McGinn M. D., Frush D. P. Increased Ototoxicity in both young and old mice. Arch Otolaryngol 1981; 107: 92
   PubMed Web of Science ®Google Scholar
• Hunter‐Duvar I. M. Electron microscopic assessment of the cochlea. Some techniques and results. Acta Otolaryngol 1978, Suppl. 351
   Google Scholar
• Keithley E. M., Feldman M. L. Hair cell counts in an age‐graded series of rat cochleas. Hearing Res 1982; 8: 249
   PubMed Web of Science ®Google Scholar
• Kohonen A. Effect of some ototoxic drugs upon the pattern and innervations of cochlear sensory cells in guinea pig. Acta Otolaryngol 1965, Suppl. 208
   Google Scholar
• Lenoir M., Shnerson A., Pujol R. Cochlear receptor development in the rat with emphasis on synaptogenesis. Anat Embryol 1980; 160: 253
   PubMedGoogle Scholar
• Marot M., Uziel A., Romand R. Ototoxicity of kanamycin in developing rats: relationship with the onset of the auditory function. Hearing Res 1980; 2: 111
   PubMed Web of Science ®Google Scholar
• Ohtahni I., Ohtsuki K., Aikawa T., Ouchi J., Nakayoshi T. A comparative study on the ototoxicity of dibekacin and tobramycin administered by intravenous infusion. Jap J Antibio 1979; 32: 990
   PubMedGoogle Scholar
• Ohtani I., Ohtsuki K., Aikawa T., Takenata M., Omata T., Ouchi J., Saito T., Nakayoshi T., Kikai S., Abe M. Ototoxicity and nephrotoxicity of aminoglycoside antibiotics administered by intravenous infusion in rabbits. Chemotherapy 1980; 28: 129
   Google Scholar
• Osako S., Tokimoto T., Matsuura S. Effects of kanamycin on the auditory evoked responses during postnatal development of the hearing of the rat. Acta Otolaryngol (Stockh) 1979; 88: 359
   PubMed Web of Science ®Google Scholar
• Pujol R., Carlier E., Devigne C. Different patterns of cochlear innervation during the development in the kitten. J Comp Neurol 1978; 117: 529
   Web of Science ®Google Scholar
• Romand R. Maturation des potentiels cochléaires dans la période périnatale chez le chat et le cobaye. J Physiol (Paris) 1971; 63: 763
   PubMedGoogle Scholar
• Romand R., Pujol R., König N., Marty R. Maturation électrophysiologique de la cochlée du chat. C R Acad Sci (Paris) 1970; 270: 2476
   Google Scholar
• Rubinstein A., Sohmer H. Latency of auditory nerve response in neonates 1–8 hours old. Ann Otol Rhinol Laryngol 1982; 91: 205
   PubMed Web of Science ®Google Scholar
• Sato K., Koeda T., Yokoda M. Histophathological study on the vestibular toxicity of dibekacin and other aminoglycosidic antibiotics. J Kanazawa Med Univ 1979a; 4: 172
   Google Scholar
• Sato K., Yokoda M., Koeda T. (1979b) Evaluation of ototoxicity of aminoglycoside antibiotics in guinea pigs by scanning electron microscopy. 11th International Congress of Chemotherapy, Boston, 1979
   Google Scholar
• Shnerson A., Devigne C., Pujol R. Age‐related changes in the C57B1/6J mouse cochlea. II. Ultrastructural findings. Develop Brain Res 1982; 2: 77
   Google Scholar
• Spoendlin H., Brun J. P. Relation of structural damage to exposure time and intensity in acoustic trauma. Acta Otolaryngol (Stockh) 1973; 75: 220
   PubMed Web of Science ®Google Scholar
• Theopold H. M. Comparative surface studies of ototoxic effects of various aminoglycoside antibiotics on the organ in the guinea‐pig. Acta Otolaryngol (Stockh) 1977; 84: 54
   Web of Science ®Google Scholar
• Uziel A., Marot M. Etude expérimentale de l'ototoxicité in utero de la dibékacine. Nouv Presse Méd 1982; 46: 3432
   Google Scholar
• Uziel A., Gabrion J., Romand R. Hair cell degeneration in guinea pigs intoxicated with kanamycin during intrauterine lifte. Arch Otorhinolaryngol 1979; 224: 187
   PubMedGoogle Scholar
• Uziel A., Romand R., Marot M. Electrophysiological study of the ototoxicity of kanamycin during development in guinea pigs. Hearing Res 1979; 1: 203
   Web of Science ®Google Scholar
• Uziel A., Romand R., Marot M. Development of cochlear potentials in rats. Audiology 1981; 20: 89
   PubMedGoogle Scholar
• Ylikoski J. Correlative studies on the cochlear pathology and hearing loss in guinea pigs after intoxication with ototoxic antibiotics. Acta Otolaryngol 1974, Suppl. 326
   Google Scholar