Abstract
1. The properties of isolated single cones were studied using the voltage-clamp technique, with two micro-electrodes inserted under visual control.
2. Single cones had input resistances, when impaled with two electrodes, of up to 270 MΩ. This is probably lower than the true membrane resistance, because of damage by the impaling electrodes. The cone capacitance was about 85 pF.
3. The cone membrane contains a time-dependent current, IB, controlled by voltage, and a separate photosensitive current.
4. The gated current, IB, is an inward current with a reversal potential around -25 mV. It is activated by hyperpolarization over the range -30 to -80 mV, and at constant voltage obeys first order (exponential) kinetics. The gating time constant is typically 50 ms at the resting potential of -45 mV, rises to 170 ms at -70 mV, and decreases for further hyperpolarization.
5. The spectral sensitivity curve of the cone light response peaks at 620 nm wave-length, and is narrower than the nomogram for vitamin A2-based pigments. The light responses of isolated cones are spectrally univariant.
6. Voltage-clamped photocurrents were recorded at various membrane potentials, for light steps of various intensities. The photocurrent reversed at around -8 mV. The time course of the photocurrent, for a given intensity, was approximately independent of voltage (although its magnitude was voltage-dependent). The shape of the peak current—voltage relation of the light-sensitive current was independent of light intensity (although its magnitude was intensity-dependent).
7. These results can be explained if: (a) light simply changes the number of photosensitive channels open, without altering the properties of an open channel; (b) the reactions controlling the production of internal transmitter, the binding of internal transmitter to the photosensitive channels, and the closing and opening of the channels are unaffected by the electric field in the cone membrane, even though at least some of these reactions take place in the membrane.
8. IB plays only a small role in shaping the cone voltage response to light.
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- Attwell D., Wilson M. Behaviour of the rod network in the tiger salamander retina mediated by membrane properties of individual rods. J Physiol. 1980 Dec;309:287–315. doi: 10.1113/jphysiol.1980.sp013509. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BROWN P. K., GIBBONS I. R., WALD G. THE VISUAL CELLS AND VISUAL PIGMENT OF THE MUDPUPPY, NECTURUS. J Cell Biol. 1963 Oct;19:79–106. doi: 10.1083/jcb.19.1.79. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bader C. R., Macleish P. R., Schwartz E. A. A voltage-clamp study of the light response in solitary rods of the tiger salamander. J Physiol. 1979 Nov;296:1–26. doi: 10.1113/jphysiol.1979.sp012988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Baylor D. A., Fuortes M. G. Electrical responses of single cones in the retina of the turtle. J Physiol. 1970 Mar;207(1):77–92. doi: 10.1113/jphysiol.1970.sp009049. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Baylor D. A., Hodgkin A. L. Detection and resolution of visual stimuli by turtle photoreceptors. J Physiol. 1973 Oct;234(1):163–198. doi: 10.1113/jphysiol.1973.sp010340. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Baylor D. A., Hodgkin A. L., Lamb T. D. The electrical response of turtle cones to flashes and steps of light. J Physiol. 1974 Nov;242(3):685–727. doi: 10.1113/jphysiol.1974.sp010731. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bortoff A., Norton A. L. An electrical model of the vertebrate photoreceptor cell. Vision Res. 1967 Mar;7(3):253–263. doi: 10.1016/0042-6989(67)90089-2. [DOI] [PubMed] [Google Scholar]
- Dennis M. J., Sargent P. B. Loss of extrasynaptic acetylcholine sensitivity upon reinnervation of parasympathetic ganglion cells. J Physiol. 1979 Apr;289:263–275. doi: 10.1113/jphysiol.1979.sp012736. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Detwiler P. B., Hodgkin A. L. Electrical coupling between cones in turtle retina. J Physiol. 1979 Jun;291:75–100. doi: 10.1113/jphysiol.1979.sp012801. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ebrey T. G., Honig B. New wavelength dependent visual pigment nomograms. Vision Res. 1977;17(1):147–151. doi: 10.1016/0042-6989(77)90213-9. [DOI] [PubMed] [Google Scholar]
- FRANKENHAEUSER B. Potassium permeability in myelinated nerve fibres of Xenopus laevis. J Physiol. 1962 Jan;160:54–61. doi: 10.1113/jphysiol.1962.sp006834. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fain G. L. Sensitivity of toad rods: Dependence on wave-length and background illumination. J Physiol. 1976 Sep;261(1):71–101. doi: 10.1113/jphysiol.1976.sp011549. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fuortes M. G., Schwartz E. A., Simon E. J. Colour-dependence of cone responses in the turtle retina. J Physiol. 1973 Oct;234(1):199–216. doi: 10.1113/jphysiol.1973.sp010341. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HODGKIN A. L., HUXLEY A. F. The components of membrane conductance in the giant axon of Loligo. J Physiol. 1952 Apr;116(4):473–496. doi: 10.1113/jphysiol.1952.sp004718. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hárosi F. I. Absorption spectra and linear dichroism of some amphibian photoreceptors. J Gen Physiol. 1975 Sep;66(3):357–382. doi: 10.1085/jgp.66.3.357. [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]
- Liebman P. A., Entine G. Visual pigments of frog and tadpole (Rana pipiens). Vision Res. 1968 Jul;8(7):761–775. doi: 10.1016/0042-6989(68)90128-4. [DOI] [PubMed] [Google Scholar]
- Noble D., Tsien R. W. The kinetics and rectifier properties of the slow potassium current in cardiac Purkinje fibres. J Physiol. 1968 Mar;195(1):185–214. doi: 10.1113/jphysiol.1968.sp008454. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Normann R. A., Perlman I. The effects of background illumination on the photoresponses of red and green cones. J Physiol. 1979 Jan;286:491–507. doi: 10.1113/jphysiol.1979.sp012633. [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]
- Schnapf J. L., McBurney R. N. Light-induced changes in membrane current in cone outer segments of tiger salamander and turtle. Nature. 1980 Sep 18;287(5779):239–241. doi: 10.1038/287239a0. [DOI] [PubMed] [Google Scholar]
- Schwartz E. A. Cones excite rods in the retina of the turtle. J Physiol. 1975 Apr;246(3):639–651. doi: 10.1113/jphysiol.1975.sp010908. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Toyoda J., Nosaki H., Tomita T. Light-induced resistance changes in single photoreceptors of Necturus and Gekko. Vision Res. 1969 Apr;9(4):453–463. doi: 10.1016/0042-6989(69)90134-5. [DOI] [PubMed] [Google Scholar]
- Werblin F. S. Time- and voltage-dependent ionic components of the rod response. J Physiol. 1979 Sep;294:613–626. doi: 10.1113/jphysiol.1979.sp012949. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Werblin F. S. Transmission along and between rods in the tiger salamander retina. J Physiol. 1978 Jul;280:449–470. doi: 10.1113/jphysiol.1978.sp012394. [DOI] [PMC free article] [PubMed] [Google Scholar]