Abstract
1. The mechanism of light adaptation was investigated by recording intracellularly from single rods in the isolated, superfused retina of the toad, Bufo marinus. Steady background lights produce decreases in rod sensitivity and changes in response wave form similar to those previously observed in the toad eyecup. 2. The sensitivity of a dark-adapted rod is halved by a background light which bleaches about 4 rhodopsins per rod per second. Since a toad rod contains over 2000 disks, a rhodopsin bleached in one disk must alter the effectiveness of rhodopsins bleached in others. This could occur if the state of adaptation in the rod were regulated by the concentration of some diffusable substance. 3. This diffusable substance cannot be Ca2+. Increases in intracellular Ca2+, produced experimentally either by increasing extracellular Ca2+ or by facilitating Ca2+ permeability into the rod with the ionophore X537A, cause a hyperpolarization of membrane potential and a decrease in response amplitude; but they do not produce changes in sensitivity and response wave form like those produced by background light. 4. Either Ca2+ is not the internal transmitter released from the disks during excitation, or the disks release or otherwise alter the concentration of a second diffusable substance, in addition to Ca2+, which regulates the state of adaptation.
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- Baylor D. A., Hodgkin A. L. Changes in time scale and sensitivity in turtle photoreceptors. J Physiol. 1974 Nov;242(3):729–758. doi: 10.1113/jphysiol.1974.sp010732. [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]
- Bertrand D., Fuortes M. G., Pochobradsky J. Actions of EGTA and high calcium on the cones in the turtle retina. J Physiol. 1978 Feb;275:419–437. doi: 10.1113/jphysiol.1978.sp012198. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brown J. E., Pinto L. H. Ionic mechanism for the photoreceptor potential of the retina of Bufo marinus. J Physiol. 1974 Feb;236(3):575–591. doi: 10.1113/jphysiol.1974.sp010453. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chabre M., Cavaggioni A. X-ray diffraction studies of retinal rods. II. Light effect on the osmotic properties. Biochim Biophys Acta. 1975 Mar 25;382(3):336–343. doi: 10.1016/0005-2736(75)90275-8. [DOI] [PubMed] [Google Scholar]
- Cohen A. I., Hall I. A., Ferrendelli J. A. Calcium and cyclic nucleotide regulation in incubated mouse retinas. J Gen Physiol. 1978 May;71(5):595–612. doi: 10.1085/jgp.71.5.595. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Célis H., Estrada S., Montal M. Model translocators for divalent and monovalent ion transport in phospholipid membranes. I. The ion permeability induced in lipid bilayers by the antibiotic X-537A. J Membr Biol. 1974;18(2):187–199. doi: 10.1007/BF01870111. [DOI] [PubMed] [Google Scholar]
- Donner K. O., Hemilä S. Excitation and adaptation in the vertebrate rod photoreceptor. Med Biol. 1978 Apr;56(2):52–63. [PubMed] [Google Scholar]
- Dowling J. E., Ripps H. Adaptation in skate photoreceptors. J Gen Physiol. 1972 Dec;60(6):698–719. doi: 10.1085/jgp.60.6.698. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Estrada S., Célis H., Calderón E., Gallo G., Montal M. Model translocators for divalent and monovalent ion transport in phospholipid membranes. II. The effects of ion translocator X-537A on the energy-conserving properties of mitochondrial membranes. J Membr Biol. 1974;18(3-4):201–218. doi: 10.1007/BF01870112. [DOI] [PubMed] [Google Scholar]
- Fain G. L., Quandt F. N., Bastian B. L., Gerschenfeld H. M. Contribution of a caesium-sensitive conductance increase to the rod photoresponse. Nature. 1978 Mar 30;272(5652):466–469. doi: 10.1038/272467a0. [DOI] [PubMed] [Google Scholar]
- Fain G. L., Quandt F. N., Gerschenfeld H. M. Calcium-dependent regenerative responses in rods. Nature. 1977 Oct 20;269(5630):707–710. doi: 10.1038/269707a0. [DOI] [PubMed] [Google Scholar]
- Fain G. L. Quantum sensitivity of rods in the toad retina. Science. 1975 Mar 7;187(4179):838–841. doi: 10.1126/science.1114328. [DOI] [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]
- Flaming D. G., Brown K. T. Effects of calcium on the intensity-response curve of toad rods. Nature. 1979 Apr 26;278(5707):852–853. doi: 10.1038/278852a0. [DOI] [PubMed] [Google Scholar]
- Greengard P. Phosphorylated proteins as physiological effectors. Science. 1978 Jan 13;199(4325):146–152. doi: 10.1126/science.22932. [DOI] [PubMed] [Google Scholar]
- HAGINS W. A., ZONANA H. V., ADAMS R. G. Local membrane current in the outer segments of squid photoreceptors. Nature. 1962 Jun 2;194:844–847. doi: 10.1038/194844a0. [DOI] [PubMed] [Google Scholar]
- HODGKIN A. L., HUXLEY A. F. Currents carried by sodium and potassium ions through the membrane of the giant axon of Loligo. J Physiol. 1952 Apr;116(4):449–472. doi: 10.1113/jphysiol.1952.sp004717. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hagins W. A., Penn R. D., Yoshikami S. Dark current and photocurrent in retinal rods. Biophys J. 1970 May;10(5):380–412. doi: 10.1016/S0006-3495(70)86308-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hagins W. A. The visual process: Excitatory mechanisms in the primary receptor cells. Annu Rev Biophys Bioeng. 1972;1:131–158. doi: 10.1146/annurev.bb.01.060172.001023. [DOI] [PubMed] [Google Scholar]
- Hagins W. A., Yoshikami S. Proceedings: A role for Ca2+ in excitation of retinal rods and cones. Exp Eye Res. 1974 Mar;18(3):299–305. doi: 10.1016/0014-4835(74)90157-2. [DOI] [PubMed] [Google Scholar]
- Kleinschmidt J., Dowling J. E. Intracellular recordings from gecko photoreceptors during light and dark adaptation. J Gen Physiol. 1975 Nov;66(5):617–648. doi: 10.1085/jgp.66.5.617. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lipton S. A., Ostroy S. E., Dowling J. E. Electrical and adaptive properties of rod photoreceptors in Bufo marinus. I. Effects of altered extracellular Ca2+ levels. J Gen Physiol. 1977 Dec;70(6):747–770. doi: 10.1085/jgp.70.6.747. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lisman J. E., Brown J. E. Effects of intracellular injection of calcium buffers on light adaptation in Limulus ventral photoreceptors. J Gen Physiol. 1975 Oct;66(4):489–506. doi: 10.1085/jgp.66.4.489. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lisman J. E., Brown J. E. Light-induced changes of sensitivity in Limulus ventral photoreceptors. J Gen Physiol. 1975 Oct;66(4):473–488. doi: 10.1085/jgp.66.4.473. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lisman J. E., Brown J. E. The effects of intracellular iontophoretic injection of calcium and sodium ions on the light response of Limulus ventral photoreceptors. J Gen Physiol. 1972 Jun;59(6):701–719. doi: 10.1085/jgp.59.6.701. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McLaughlin S., Eisenberg M. Antibiotics and membrane biology. Annu Rev Biophys Bioeng. 1975;4(00):335–366. doi: 10.1146/annurev.bb.04.060175.002003. [DOI] [PubMed] [Google Scholar]
- Meech R. W., Thomas R. C. The effect of calcium injection on the intracellular sodium and pH of snail neurones. J Physiol. 1977 Mar;265(3):867–879. doi: 10.1113/jphysiol.1977.sp011749. [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]
- RUSHTON W. A. VISUAL ADAPTATION. Proc R Soc Lond B Biol Sci. 1965 Mar 16;162:20–46. doi: 10.1098/rspb.1965.0024. [DOI] [PubMed] [Google Scholar]
- Winkler B. S. Calcium and the fast and slow components of P3 of the electroretinogram of the isolated rat retina. Vision Res. 1974 Jan;14(1):9–15. doi: 10.1016/0042-6989(74)90110-2. [DOI] [PubMed] [Google Scholar]
- Woodruff M. L., Bownds M. D. Amplitude, kinetics, and reversibility of a light-induced decrease in guanosine 3',5'-cyclic monophosphate in frog photoreceptor membranes. J Gen Physiol. 1979 May;73(5):629–653. doi: 10.1085/jgp.73.5.629. [DOI] [PMC free article] [PubMed] [Google Scholar]