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. 1969 Jan 1;53(1):115–130. doi: 10.1085/jgp.53.1.115

Further Studies on the Roles of Sodium and Potassium in the Generation of the Electro-Olfactogram

Effects of mono-, di-, and trivalent cations

S F Takagi 1, H Kitamura 1, K Imai 1, H Takeuchi 1
PMCID: PMC2202899  PMID: 5761869

Abstract

In the negative EOG-generating process a cation which can substitute for Na+ was sought among the monovalent ions, Li+, Rb+, Cs+, NH4 +, and TEA+, the divalent ions, Mg++, Ca++, Sr++, Ba++, Zn++, Cd++, Mn++, Co++, and Ni++, and the trivalent ions, Al+++ and Fe+++. In Ringer solutions in which Na+ was replaced by one of these cations the negative EOG's decreased in amplitude and could not maintain the original amplitudes. In K+-Ringer solution in which Na+ was replaced by K+, the negative EOG's reversed their polarity. Recovery of these reversed potentials was examined in modified Ringer solutions in which Na+ was replaced by one of the above cations. Complete recovery was found only in the normal Ringer solution. Thus, it was clarified that Na+ plays an irreplaceable role in the generation of the negative EOG's. The sieve hypothesis which was valid for the positive EOG-generating membrane or IPSP was not found applicable in any form to the negative EOG-generating membrane. The reversal of the negative EOG's found in K+- , Rb+- , and Ba++-Ringer solutions was attributed to the exit of the internal K+. It is, however, not known whether or not Cl- permeability increases in these Na+-free solutions and contributes to the generation of the reversed EOG's.

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Selected References

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  1. ARAKI T., ITO M., OSCARSSON O. Anion permeability of the synaptic and non-synaptic motoneurone membrane. J Physiol. 1961 Dec;159:410–435. doi: 10.1113/jphysiol.1961.sp006818. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. ASANO T., HURLBUT W. P. Effects of potassium, sodium, and azide on the ionic movements that accompany activity in frog nerves. J Gen Physiol. 1958 Jul 20;41(6):1187–1203. doi: 10.1085/jgp.41.6.1187. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. DIAMOND J., GRAY J. A., INMAN D. R. The relation between receptor potentials and the concentration of sodium ions. J Physiol. 1958 Jul 14;142(2):382–394. doi: 10.1113/jphysiol.1958.sp006024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. EDWARDS C., TERZUOLO C. A., WASHIZU H. THE EFFECT OF CHANGES OF THE IONIC ENVIRONMENT UPON AN ISOLATED CRUSTACEAN SENSORY NEURON. J Neurophysiol. 1963 Nov;26:948–957. doi: 10.1152/jn.1963.26.6.948. [DOI] [PubMed] [Google Scholar]
  5. Eguchi E. Rhabdom structure and receptor potentials in single crayfish retinular cells. J Cell Physiol. 1965 Dec;66(3):411–429. doi: 10.1002/jcp.1030660314. [DOI] [PubMed] [Google Scholar]
  6. FATT P., GINSBORG B. L. The ionic requirements for the production of action potentials in crustacean muscle fibres. J Physiol. 1958 Aug 6;142(3):516–543. doi: 10.1113/jphysiol.1958.sp006034. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. FATT P., KATZ B. The electrical properties of crustacean muscle fibres. J Physiol. 1953 Apr 28;120(1-2):171–204. doi: 10.1113/jphysiol.1953.sp004884. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. FURUKAWA T., HANAWA I. Effects of some common cations on electroretinogram of the toad. Jpn J Physiol. 1955 Dec 15;5(4):289–300. doi: 10.2170/jjphysiol.5.289. [DOI] [PubMed] [Google Scholar]
  9. Gesteland R. C., Lettvin J. Y., Pitts W. H. Chemical transmission in the nose of the frog. J Physiol. 1965 Dec;181(3):525–559. doi: 10.1113/jphysiol.1965.sp007781. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. HAGIWARA S., NAKA K. I. THE INITIATION OF SPIKE POTENTIAL IN BARNACLE MUSCLE FIBERS UNDER LOW INTRACELLULAR CA++. J Gen Physiol. 1964 Sep;48:141–162. doi: 10.1085/jgp.48.1.141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. HIGASHINO S., TAKAGI S. F. THE EFFECT OF ELECTROTONUS ON THE OLFACTORY EPITHELIUM. J Gen Physiol. 1964 Nov;48:323–335. doi: 10.1085/jgp.48.2.323. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. ITO M., KOSTYUK P. G., OSHIMA T. Further study on anion permeability of inhibitory post-synaptic membrane of cat motoneurones. J Physiol. 1962 Oct;164:150–156. doi: 10.1113/jphysiol.1962.sp007009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. KIKUCHI R., NAITO K., TANAKA I. Effect of sodium and potassium ions on the electrical activity of single cells in the lateral eye of the horseshoe crab. J Physiol. 1962 May;161:319–343. doi: 10.1113/jphysiol.1962.sp006889. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. NISHI S., SOEDA H., KOKETSU K. EFFECT OF ALKALI-EARTH CATIONS ON FROG SPINAL GANGLION CELL. J Neurophysiol. 1965 May;28:457–472. doi: 10.1152/jn.1965.28.3.457. [DOI] [PubMed] [Google Scholar]
  15. OTTOSON D. Analysis of the electrical activity of the olfactory epithelium. Acta Physiol Scand Suppl. 1955;35(122):1–83. [PubMed] [Google Scholar]
  16. OTTOSON D. THE EFFECT OF SODIUM DEFICIENCY ON THE RESPONSE OF THE ISOLATED MUSCLE SPINDLE. J Physiol. 1964 May;171:109–118. doi: 10.1113/jphysiol.1964.sp007365. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. TAKAGI S. F., SHIBUYA T. The electrical activity of the olfactory epithelium studied with micro- and macro-electrodes. Jpn J Physiol. 1960 Aug 15;10:385–395. doi: 10.2170/jjphysiol.10.385. [DOI] [PubMed] [Google Scholar]
  18. TAKAGI S. F., YAJIMA T. ELECTRICAL ACTIVITY AND HISTOLOGICAL CHANGE IN THE DEGENERATING OLFACTORY EPITHELIUM. J Gen Physiol. 1965 Mar;48:559–569. doi: 10.1085/jgp.48.4.559. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. TAKAGI S. F., YAJIMA T. ELECTRICAL RESPONSES TO ODOURS OF DEGENERATING OLFACOTRY EPITHELIUM. Nature. 1964 Jun 20;202:1220–1220. doi: 10.1038/2021220a0. [DOI] [PubMed] [Google Scholar]
  20. TUCKER D. Physical variables in the olfactory stimulation process. J Gen Physiol. 1963 Jan;46:453–489. doi: 10.1085/jgp.46.3.453. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Takagi S. F., Wyse G. A., Kitamura H., Ito K. The role of sodium and potassium ions in the generation of the electro-olfactogram. J Gen Physiol. 1968 Apr;51(4):552–578. doi: 10.1085/jgp.51.4.552. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Takagi S. F., Wyse G. A., Yajima T. Anion permeability of the olfactory receptive membrane. J Gen Physiol. 1966 Nov;50(2):473–489. doi: 10.1085/jgp.50.2.473. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Tucker D., Shibuya T. A physiologic and pharmacologic study of olfactory receptors. Cold Spring Harb Symp Quant Biol. 1965;30:207–215. doi: 10.1101/sqb.1965.030.01.023. [DOI] [PubMed] [Google Scholar]
  24. WERMAN R., GRUNDFEST H. Graded and all-or-none electrogenesis in arthropod muscle. II. The effects of alkali-earth and onium ions on lobster muscle fibers. J Gen Physiol. 1961 May;44:997–1027. doi: 10.1085/jgp.44.5.997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. WERMAN R., McCANN F. V., GRUNDFEST H. Graded and all-or-none electrogenesis in arthropod muscle. I. The effects of alkali-earth cations on the neuromuscular system of Romalea microptera. J Gen Physiol. 1961 May;44:979–995. doi: 10.1085/jgp.44.5.979. [DOI] [PMC free article] [PubMed] [Google Scholar]

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