Action of Streptomycin and Calcium on the Apical Membrane of Hair Cells of the Frog Isolated Semicircular Canal

References

• Baker P. F., Hodgkin A. L., Ridgway E. B. Depolarization and calcium entry in squid gigant axons. J Physiol 1971; 288: 709
   Google Scholar
• Beani L., Bianchi C., Ledda F. The effect of 2–4 DNP on neuromuscular transmission. Br J Pharmacol 1966; 27: 299
   Web of Science ®Google Scholar
• Bernard C. Electrical activity of isolated semicircular canal in the frog: action of streptomycin. Pflügers Arch 1980; 388: 93
   PubMed Web of Science ®Google Scholar
• Berg K. The toxic effect of streptomycin on the eighth cranial nerve. Am ORL 1949; 58: 448
   Google Scholar
• Casella C., Taglietti V. Aspects of mechano-electrical transduction in frog semicircular canals. Istituto Lombardo (Rend Sc)B 1976; 110: 78
   Google Scholar
• Caussé R. Action toxique vestibulaire et cochléaire de la streptomycine au point de vue expérimentale. Am Otolaryngol 1949; 66: 518
   Google Scholar
• Caussé R., Gondet I. Modifications histologiques de l'appareil vestibulaire sous l'influence de la streptomycine. CR Acad Sci 1949; 228: 1253
   Google Scholar
• Clusin W., Spray D. C., Bennett M. V. L. Activation of a voltage insensitive conductance by inward calcium current. Nature 1975; 256: 425
   PubMed Web of Science ®Google Scholar
• Corey D. P., Hudspeth A. J. Ionic basis of the receptor potential in a vertebrate hair cell. Nature 1979; 281: 675
   PubMed Web of Science ®Google Scholar
• Davis H., Deatherage B. H., Rosenblut B., Fernandez C., Kimura R., Smith C. A. Modification of cochlear potentials produced by streptomycin poisoning and by extensive venous obstruction. Laryngoscope 1958; 68: 596
   PubMedGoogle Scholar
• Davis H. A model transducer action in the cochlea. Cold Spring Harbor Symp Quant Biol 1965; 30: 181
   PubMedGoogle Scholar
• Gallais A., Caston J., Zittoun A. Vestibular effects antibiotics introduced in the inner ear. Acta Otolaryngol (Stockh) 1979; 87: 517
   PubMed Web of Science ®Google Scholar
• Harada Y., Musso E., Mird E. Action of streptomycin, dihydrostreptomycin, neomycin and kanamy-cin on the ampullar receptors of the frog. Acta Otolatyngol (Stockh) 1967; 4: 327
   Google Scholar
• Harada Y., Sugimoto Y. Metabolic disorder of otoconia after streptomycin intoxication. Acta Otolaryngol (Stockh) 1977; 84: 65
   PubMed Web of Science ®Google Scholar
• Hawkins J. E. Cochlear signs of streptomycin intoxication. J Pharm Exp Therap 1950; 38: 100
   Google Scholar
• Hawkins J. E., Lurie M. H. The ototoxicity of streptomycin. Ann ORL 1952; 61: 789
   Google Scholar
• Hillman D. E. Light and electron microscopial study of the relationship between the cerebellum and the vestibular organ of the frog. Exp Brain Res 1969; 9: 1
   PubMed Web of Science ®Google Scholar
• Hudspeth A. J., Corey D. P. Sensitivity, polarity and conductance change in the response of vertebrate hair cells to controlled mechanical stimuli. Proc Natl Acad Sci USA 1977; 74: 2407
   PubMed Web of Science ®Google Scholar
• Katz B., Miledi R. Tetrodotoxin and neuromuscular transmission. Proc R Soc Lond (Biol) 1967; 167: 8
   PubMed Web of Science ®Google Scholar
• Lindeman H. H. Regional differences in sensitivity of the vestibular sensory epithelia to ototoxic antibiotics. Acta Otolaryngol (Stockh) 1969; 67: 177
   PubMed Web of Science ®Google Scholar
• Lowenstein O., Wersall J. A functional interpretation of the electron microscopic structure of the sensory hairs in the cristae of the elasmobranch Raja clavata in terms of directional sensitivity. Nature (Lond) 1959; 184: 1807
   Web of Science ®Google Scholar
• Matsuura S., Ikeda K., Furukawa T. Ouabain and streptomycin: their different loci of action on saccular hair cells in Goldfish. Science 1968; 160: 1117
   PubMed Web of Science ®Google Scholar
• Matsuura S., Ikeda K., Furukawa T. Effects of streptomycin, kanamycin, quinine and other drugs on the microphonic potentials of goldfish sacculus. Jap J Physiol 1971; 21: 579
   PubMedGoogle Scholar
• Meech R. W., Standen N. B. Potassium activation in Helix aspersa neurones under voltage clamps: a component mediated by calcium influx. J Physiol (Lond) 1975; 249: 211
   Google Scholar
• Pittinger C. B. pH and streptomycin influence upon ionic calcium in serum. Anest Analg 1970; 49(4)540
   PubMed Web of Science ®Google Scholar
• Rapuzzi G., Casella C. L'action du BaCl2 sur le récepteur ampullaire des canaux semi-circulaires isolés de Grenouille. J Physiol (Paris) 1967; 59: 480
   PubMedGoogle Scholar
• Rossi M. L., Valli P., Casella C. Post-synaptic potentials recorded from afferent nerve fibres of the posterior semicircular canal in the frog. Brain Res 1977; 135: 67
   PubMed Web of Science ®Google Scholar
• Sand O. Effects of different ionic environments on the mechanosensitivity of lateral line organs in the Mudpuppy. J Comp Physiol 1975; 102: 27
   Web of Science ®Google Scholar
• Sand O., Ozawa S., Hagiwara S. Electrical and mechanical stimulation of hair cells in the Mudpuppy. J Comp Physiol 1975; 102: 13
   Web of Science ®Google Scholar
• Steinbach A. B., Bennett M. V. L. Effects of divalent ions and drugs on synaptic transmission in phasic electroreceptors in a Mormyrid fish. J Gen Physiol 1971; 58: 580
   PubMed Web of Science ®Google Scholar
• Suarez-Kurtz G. Inhibition of membrane calcium activation by neomycin and streptomycin in Crab muscle fibers. Pflügers Arch 1974; 349: 337
   PubMed Web of Science ®Google Scholar
• Tyberghein J. Influence of some Streptomyces antibiotics on the cochlear microphonics in the Guinea pig. Acta Orolaryngol (Stockh) 1962; 171: 1, Suppl
   PubMedGoogle Scholar
• Valli P., Taglietti V., Rossi M. L. Effects of d-tubocurarine on the ampullar receptors of the frog. Acta Otolaryngol (Stockh) 1974; 78: 51
   PubMed Web of Science ®Google Scholar
• Valli P., Zucca G. The origin of slow potentials in semicircular canals of the frog. Acta Otolaryngol (Stockh) 1976; 81: 395
   PubMed Web of Science ®Google Scholar
• Valli P., Zucca G., Casella C. K+ as labyrinthine current carrier. IRCS Med Sci 1976; 4: 455
   Google Scholar
• Valli P., Zucca G., Casella C. The importance of K+ in the function of frog semicircular canals. Acta Otolaryngol (Stockh) 1977; 84: 344
   PubMed Web of Science ®Google Scholar
• Valli P., Zucca G., Casella C. Lonic composition of the endolymph and sensory transduction in labyrinthine organs. Acta Otolaryngol (Stockh) 1979; 78: 466
   Google Scholar
• Wersäll J., Hawkins J. E. The vestibular sensory epithelia in the cat labyrinth and their reactions in chronic streptomycin intoxication. Acta Otolaryngol (Stockh) 1962; 54: 1
   PubMedGoogle Scholar
• Wersäll J., Flock Å. Suppression and restoration of the microphonic output from the lateral line organ after local application of streptomycin. Life Sciences 1964; 3: 1151
   Web of Science ®Google Scholar