Abstract
1. Responses of salamander cones to steps of light on their surrounding area were intracellularly recorded through micropipettes filled with 2 M-potassium acetate or 2 M-potassium chloride. 2. Using 2 M-potassium acetate, cone step responses showed a larger relaxation for a 1100 micrometers diameter spot than for a 100 micrometers spot, but dim annular illumination failed to evoke any detectable response. With 2 M-potassium chloride the larger spot or an anulus evoked responses that were mainly or purely depolarizing, respectively, while the responses to the smaller spot were still hyperpolarizing. 3. The depolarizing response to annular illumination had an increased amplitude immediately after discontinuing the injection of inward current through a micropipette filled with 2 M-potassium chloride. 4. Depolarization by extrinsic current reversed the polarity of the depolarizing response to annular illumination. 5. It is suggested that the enhancement of the depolarizing influence of the surround is due to an increase in the intracellular concentration of chloride ions, which issue from the electrodes by passive diffusion or electrophoresis. Taking into consideration the effect of depolarizing current, it would follow that surround illumination induces an increase in the chloride conductance of the cone membrane. 6. Preliminary observations on the properties of the enhanced surround response reveal a slow time course and a receptive field of more than 270 micrometers radius.
Full text
PDF










Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- 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]
- Bortoff A. Localization of slow potential responses in the Necturus retina. Vision Res. 1964 Dec;4(11):627–635. doi: 10.1016/0042-6989(64)90048-3. [DOI] [PubMed] [Google Scholar]
- Lasansky A. Contacts between receptors and electrophysiologically identified neurones in the retina of the larval tiger salamander. J Physiol. 1978 Dec;285:531–542. doi: 10.1113/jphysiol.1978.sp012587. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lasansky A., Marchiafava P. L. Light-induced resistance changes in retinal rods and cones of the tiger salamander. J Physiol. 1974 Jan;236(1):171–191. doi: 10.1113/jphysiol.1974.sp010429. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lasansky A. Organization of the outer synaptic layer in the retina of the larval tiger salamander. Philos Trans R Soc Lond B Biol Sci. 1973;265(872):471–489. doi: 10.1098/rstb.1973.0033. [DOI] [PubMed] [Google Scholar]
- Lasansky A., Vallerga S. Horizontal cell responses in the retina of the larval tiger salamander. J Physiol. 1975 Sep;251(1):145–165. doi: 10.1113/jphysiol.1975.sp011085. [DOI] [PMC free article] [PubMed] [Google Scholar]
- O'Bryan P. M. Properties of the depolarizing synaptic potential evoked by peripheral illumination in cones of the turtle retina. J Physiol. 1973 Nov;235(1):207–223. doi: 10.1113/jphysiol.1973.sp010385. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Piccolino M., Gerschenfeld H. M. Activation of a regenerative calcium conductance in turtle cones by peripheral stimulation. Proc R Soc Lond B Biol Sci. 1978 May 16;201(1144):309–315. doi: 10.1098/rspb.1978.0048. [DOI] [PubMed] [Google Scholar]
- Saito T., Kondo H., Toyoda J. I. Ionic mechanisms of two types of on-center bipolar cells in the carp retina. I. The responses to central illumination. J Gen Physiol. 1979 Jan;73(1):73–90. doi: 10.1085/jgp.73.1.73. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Weight F. F., Padjen A. Slow synaptic inhibition: evidence for synaptic inactivation of sodium conductance in sympathetic ganglion cells. Brain Res. 1973 May 30;55(1):219–224. doi: 10.1016/0006-8993(73)90505-2. [DOI] [PubMed] [Google Scholar]
- Weight F. F., Votava J. Slow synaptic excitation in sympathetic ganglion cells: evidence for synaptic inactivation of potassium conductance. Science. 1970 Nov 13;170(3959):755–758. doi: 10.1126/science.170.3959.755. [DOI] [PubMed] [Google Scholar]
- 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]

