Two components of electrical dark noise in toad retinal rod outer segments.

1. Physiological noise in the visual transduction mechanism was studied by recording membrane current from single rod outer segments in pieces of isolated toad retina. 2. The inward current in darkness showed spontaneous fluctuations which disappeared during the response to bright light. 3. The dark noise consisted of two components, a continuous fluctuation of rms amplitude about 0.2 pA and occasional discrete events about 1 pA in size. 4. Intervals between discrete events followed the exponential distribution expected of a Poisson process with a mean rate of about one event per 50 sec (20 degrees C). 5. The amplitude and power spectrum of the discrete events resembled those of single photon effects in the same rod, suggesting that discrete events may arise from spontaneous activation of single rhodopsin molecules. 6. The temperature dependence of the mean frequency of occurrence of discrete events gave an activation energy of 22 kcal mole‐1, probably characteristic of thermal isomerization of rhodopsin. 7. The variance of the continuous component of the dark noise rose linearly with the length of the outer segment drawn into the suction electrode, indicating that this component is generated in the outer segment. 8. The power spectrum of a rod's continuous noise was usually fitted by the square of a Lorentzian with the same time constant as that of the four first‐order delays in the cell's single photon response. The shot effects composing the continuous component thus appear to be shaped by two of four sequential processes in transduction. 9. The variance and spectrum of the continuous noise are interpreted to reflect shot effects about 1/400 the size of a single photon effect occurring at a frequency of 6 x 10(3) sec‐1. 10. The rod's flash sensitivity was halved by a steady light to giving about 8 photoisomerizations sec‐1. The much lower mean rate of discrete events indicates that Io in increment sensitivity experiments on individual receptors is not set by thermal activation of rhodopsin. 11. Values of sensitivity and time‐to‐peak flash response collected from many cells in darkness were correlated by the same power law relation obtaining in the presence of backgrounds. The correlation observed would be explained if a single variable controlled both the gain and time scale of several stages of the transduction mechanism in background light and in darkness.

[1]  M. Muir Physical Chemistry , 1888, Nature.

[2]  S. Rice Mathematical analysis of random noise , 1944 .

[3]  R. Hubbard THE THERMAL STABILITY OF RHODOPSIN AND OPSIN , 1958, The Journal of general physiology.

[4]  A. Hodgkin,et al.  Changes in time scale and sensitivity in the ommatidia of Limulus , 1964, The Journal of physiology.

[5]  M. Rosenlicht Introduction to Analysis , 1970 .

[6]  D. Baylor,et al.  Electrical responses of single cones in the retina of the turtle , 1970, The Journal of physiology.

[7]  W. A. Hagins,et al.  Kinetics of the photocurrent of retinal rods. , 1972, Biophysical journal.

[8]  H. Barlow Dark and Light Adaptation: Psychophysics , 1972 .

[9]  B Katz,et al.  The statistical nature of the acetylcholine potential and its molecular components , 1972, The Journal of physiology.

[10]  A. Hodgkin,et al.  Detection and resolution of visual stimuli by turtle photoreceptors , 1973, The Journal of physiology.

[11]  R. Cone The Internal Transmitter Model for Visual Excitation: Some Quantitative Implications , 1973 .

[12]  C. Stevens,et al.  Voltage clamp analysis of acetylcholine produced end‐plate current fluctuations at frog neuromuscular junction , 1973, The Journal of physiology.

[13]  A. Hodgkin,et al.  Reconstruction of the electrical responses of turtle cones to flashes and steps of light , 1974, The Journal of physiology.

[14]  L. Pinto,et al.  Ionic mechanism for the photoreceptor potential of the retina of Bufo marinus , 1974, The Journal of physiology.

[15]  A. Hodgkin,et al.  The electrical response of turtle cones to flashes and steps of light , 1974, The Journal of physiology.

[16]  A. Hodgkin,et al.  Changes in time scale and sensitivity in turtle photoreceptors , 1974, The Journal of physiology.

[17]  F. I. Hárosi Absorption spectra and linear dichroism of some amphibian photoreceptors , 1975, The Journal of general physiology.

[18]  I. Willis PHOTOSENSITIVITY , 1975, International journal of dermatology.

[19]  A. Hodgkin,et al.  Spontaneous voltage fluctuations in retinal cones and bipolar cells , 1975, Nature.

[20]  E. Pugh Rhodopsin flash photolysis in man. , 1975, The Journal of physiology.

[21]  G. Fain,et al.  Quantum sensitivity of rods in the toad retina. , 1975, Science.

[22]  G. Fain,et al.  Sensitivity of toad rods: Dependence on wave‐length and background illumination. , 1976, The Journal of physiology.

[23]  T. Lamb,et al.  The relation between intercellular coupling and electrical noise in turtle photoreceptors. , 1976, The Journal of physiology.

[24]  E. A. Schwartz,et al.  Electrical properties of the rod syncytium in the retina of the turtle. , 1976, The Journal of physiology.

[25]  T. Lamb,et al.  Analysis of electrical noise in turtle cones , 1977, The Journal of physiology.

[26]  E. A. Schwartz,et al.  Voltage noise observed in rods of the turtle retina , 1977, The Journal of physiology.

[27]  J. Ashmore,et al.  Dark noise in retinal bipolar cells and stability of rhodopsin in rods , 1977, Nature.

[28]  D. Baylor,et al.  Light-induced fluctuations in membrane current of single toad rod outer segments , 1977, Nature.

[29]  F. Wong Nature of light-induced conductance changes in ventral photoreceptors of Limulus , 1978, Nature.

[30]  D. Baylor,et al.  Responses of retinal rods to single photons. , 1979, The Journal of physiology.

[31]  G. Fain,et al.  Light adaptation in toad rods: requirement for an internal messenger which is not calcium. , 1979, The Journal of physiology.

[32]  D. Baylor,et al.  Thermal activation of the visual transduction mechanism in retinal rods , 1979, Nature.

[33]  D. Baylor,et al.  The membrane current of single rod outer segments , 1979, Vision Research.

[34]  G. H. Gold Photoreceptor coupling in retina of the toad, Bufo marinus. II. Physiology. , 1979, Journal of neurophysiology.

[35]  A. Hodgkin,et al.  Temporal and spatial characteristics of the voltage response of rods in the retina of the snapping turtle , 1980, The Journal of physiology.