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. 1971 Aug 1;58(2):163–189. doi: 10.1085/jgp.58.2.163

S-Potentials in the Skate Retina

Intracellular recordings during light and dark adaptation

John E Dowling 1, Harris Ripps 1
PMCID: PMC2226016  PMID: 5559621

Abstract

The S-potentials recorded intracellularly from the all-rod retina of the skate probably arise from the large horizontal cells situated directly below the layer of receptors. These cells hyperpolarize in response to light, irrespective of stimulus wavelength, and the responses in photopic as well as scotopic conditions were found to be subserved by a single photopigment with λmax = 500 nm. The process of adaptation was studied by recording simultaneously the threshold responses and membrane potentials of S-units during both light and dark adaptation. The findings indicate that the sensitivity of S-units, whether measured upon steady background fields or in the course of dark adaptation, exhibits changes similar to those demonstrated previously for the ERG b-wave and ganglion cell discharge. However, the membrane potential level of the S-unit and its sensitivity to photic stimulation varied independently for all the adapting conditions tested. It appears, therefore, that visual adaptation in the skate retina occurs before the S-unit is reached, i.e., at the receptors themselves.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Baylor D. A., Fuortes M. G., O'Bryan P. M. Receptive fields of cones in the retina of the turtle. J Physiol. 1971 Apr;214(2):265–294. doi: 10.1113/jphysiol.1971.sp009432. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Boynton R. M., Whitten D. N. Visual adaptation in monkey cones: recordings of late receptor potentials. Science. 1970 Dec 25;170(3965):1423–1426. doi: 10.1126/science.170.3965.1423. [DOI] [PubMed] [Google Scholar]
  3. Brown K. T., Murakami M. Rapid effects of light and dark adaptation upon the receptive field organization of S-potentials and late receptor potentials. Vision Res. 1968 Sep;8(9):1145–1171. doi: 10.1016/0042-6989(68)90024-2. [DOI] [PubMed] [Google Scholar]
  4. Brown K. T., Watanabe K., Murakami M. The early and late receptor potentials of monkey cones and rods. Cold Spring Harb Symp Quant Biol. 1965;30:457–482. doi: 10.1101/sqb.1965.030.01.045. [DOI] [PubMed] [Google Scholar]
  5. Byzov A. L. Gorizontal'nye kletki setchatki-reguliatory sinapticheskoi peredachi. Fiziol Zh SSSR Im I M Sechenova. 1967 Sep;53(9):1115–1124. [PubMed] [Google Scholar]
  6. Cone R. A., Brown P. K. Spontaneous regeneration of rhodopsin in the isolated rat retina. Nature. 1969 Mar 1;221(5183):818–820. doi: 10.1038/221818a0. [DOI] [PubMed] [Google Scholar]
  7. DARTNALL H. J. A. The interpretation of spectral sensitivity curves. Br Med Bull. 1953;9(1):24–30. doi: 10.1093/oxfordjournals.bmb.a074302. [DOI] [PubMed] [Google Scholar]
  8. DOWLING J. E. NEURAL AND PHOTOCHEMICAL MECHANISMS OF VISUAL ADAPTATION IN THE RAT. J Gen Physiol. 1963 Jul;46:1287–1301. doi: 10.1085/jgp.46.6.1287. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Dowling J. E., Ripps H. Visual adaptation in the retina of the skate. J Gen Physiol. 1970 Oct;56(4):491–520. doi: 10.1085/jgp.56.4.491. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dowling J. E. The site of visual adaptation. Science. 1967 Jan 20;155(3760):273–279. doi: 10.1126/science.155.3760.273. [DOI] [PubMed] [Google Scholar]
  11. GOURAS P. Graded potentials of bream retina. J Physiol. 1960 Jul;152:487–505. doi: 10.1113/jphysiol.1960.sp006504. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Glantz R. M. Light adaptation in the photoreceptor of the crayfish, Procambarus clarki. Vision Res. 1968 Nov;8(11):1407–1421. doi: 10.1016/0042-6989(68)90087-4. [DOI] [PubMed] [Google Scholar]
  13. Kaneko A. Physiological and morphological identification of horizontal, bipolar and amacrine cells in goldfish retina. J Physiol. 1970 May;207(3):623–633. doi: 10.1113/jphysiol.1970.sp009084. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. MACNICHOL E. J., SVAETICHIN G. Electric responses from the isolated retinas of fishes. Am J Ophthalmol. 1958 Sep;46(3 Pt 2):26–46. doi: 10.1016/0002-9394(58)90053-9. [DOI] [PubMed] [Google Scholar]
  15. Naka K. I. Factors influencing the time course of S-potentials resulting from brief flashes. J Physiol. 1969 Feb;200(2):373–385. doi: 10.1113/jphysiol.1969.sp008699. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Naka K. I. Receptive field mechanism in the vertebrate retina. Science. 1971 Feb 19;171(3972):691–693. doi: 10.1126/science.171.3972.691. [DOI] [PubMed] [Google Scholar]
  17. Naka K. I., Rushton W. A. S-potential and dark adaptation in fish. J Physiol. 1968 Jan;194(1):259–269. doi: 10.1113/jphysiol.1968.sp008406. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Naka K. I., Rushton W. A. S-potentials from luminosity units in the retina of fish (Cyprinidae). J Physiol. 1966 Aug;185(3):587–599. doi: 10.1113/jphysiol.1966.sp008003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Norton A. L., Spekreijse H., Wolbarsht M. L., Wagner H. G. Receptive field organization of the S-potential. Science. 1968 May 31;160(3831):1021–1022. doi: 10.1126/science.160.3831.1021. [DOI] [PubMed] [Google Scholar]
  20. Penn R. D., Hagins W. A. Signal transmission along retinal rods and the origin of the electroretinographic a-wave. Nature. 1969 Jul 12;223(5202):201–204. doi: 10.1038/223201a0. [DOI] [PubMed] [Google Scholar]
  21. RUSHTON W. A. Increment threshold and dark adaptation. J Opt Soc Am. 1963 Jan;53:104–109. doi: 10.1364/josa.53.000104. [DOI] [PubMed] [Google Scholar]
  22. RUSHTON W. A. THE SENSITIVITY OF RODS UNDER ILLUMINATION. J Physiol. 1965 May;178:141–160. doi: 10.1113/jphysiol.1965.sp007620. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Ripps H., Weale R. A. Flash bleaching of rhodopsin in the human retina. J Physiol. 1969 Jan;200(1):151–159. doi: 10.1113/jphysiol.1969.sp008686. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Ripps H., Weale R. A. The photophysiology of vertebrate color vision. Photophysiology. 1970;5:127–168. [PubMed] [Google Scholar]
  25. Steinberg R. H. Rod-cone interaction in S-potentials from the cat retina. Vision Res. 1969 Nov;9(11):1331–1344. doi: 10.1016/0042-6989(69)90070-4. [DOI] [PubMed] [Google Scholar]
  26. Steinberg R. H., Schmidt R. Identification of horizontal cells as S-potential generators in the cat retina by intracellular dye injection. Vision Res. 1970 Sep;10(9):817–820. doi: 10.1016/0042-6989(70)90160-4. [DOI] [PubMed] [Google Scholar]
  27. TOMITA T., TOSAKA T., WATANABE K., SATO Y. The fish EIRG in response to different types of illumination. Jpn J Physiol. 1958 Mar 30;8(1):41–50. doi: 10.2170/jjphysiol.8.41. [DOI] [PubMed] [Google Scholar]
  28. Tomita T. Electrophysiological study of the mechanisms subserving color coding in the fish retina. Cold Spring Harb Symp Quant Biol. 1965;30:559–566. doi: 10.1101/sqb.1965.030.01.054. [DOI] [PubMed] [Google Scholar]
  29. Weinstein G. W., Hobson R. R., Dowling J. E. Light and dark adaptation in the isolated rat retina. Nature. 1967 Jul 8;215(5097):134–138. doi: 10.1038/215134a0. [DOI] [PubMed] [Google Scholar]
  30. Werblin F. S. Adaptation in a vertebrate retina: intracellular recording in Necturus. J Neurophysiol. 1971 Mar;34(2):228–241. doi: 10.1152/jn.1971.34.2.228. [DOI] [PubMed] [Google Scholar]
  31. Werblin F. S., Dowling J. E. Organization of the retina of the mudpuppy, Necturus maculosus. II. Intracellular recording. J Neurophysiol. 1969 May;32(3):339–355. doi: 10.1152/jn.1969.32.3.339. [DOI] [PubMed] [Google Scholar]
  32. Witkovsky P. A comparison of ganglion cell and S-potential response properties in carp retina. J Neurophysiol. 1967 May;30(3):546–561. doi: 10.1152/jn.1967.30.3.546. [DOI] [PubMed] [Google Scholar]

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