The DOI matches its Crossref record; 16 of the 16 references it cites were found in a registry or an index.
The electrical response of turtle cones to flashes and steps of light
Open accessAbstract
1. The linear response of turtle cones to weak flashes or steps of light was usually well fitted by equations based on a chain of six or seven reactions with time constants varying over about a 6‐fold range. 2. The temperature coefficient (Q10) of the reciprocal of the time to peak of the response to a flash was 1·8 (15‐25° C), corresponding to an activation energy of 10 kcal/mole. 3. Electrical measurements with one internal electrode and a balancing circuit gave the following results on red‐sensitive cones of high resistance: resistance across cell surface in dark 50–170 MΩ; time constant in dark 4‐6·5 msec. The effect of a bright light was to increase the resistance and time constant by 10–30%. 4. If the cell time constant, resting potential and maximum hyperpolarization are known, the fraction of ionic channels blocked by light at any instant can be calculated from the hyperpolarization and its rate of change. At times less than 50 msec the shape of this relation is consistent with the idea that the concentration of a blocking molecule which varies linearly with light intensity is in equilibrium with the fraction of ionic channels blocked. 5. The rising phase of the response to flashes and steps of light covering a 10 5‐fold range of intensities is well fitted by a theory in which the essential assumptions are that (i) light starts a linear chain of reactions leading to the production of a substance which blocks ionic channels in the outer segment, (ii) an equilibrium between the blocking molecules and unblocked channels is established rapidly, and (iii) the electrical properties of the cell can be represented by a simple circuit with a time constant in the dark of about 6 msec. 6. Deviations from the simple theory which occur after 50 msec are attributed partly to a time‐dependent desensitization mechanism and partly to a change in saturation potential resulting from a voltage‐dependent change in conductance. 7. The existence of several components in the relaxation of the potential to its resting level can be explained by supposing that the ‘substance’ which blocks light sensitive ionic channels is inactivated in a series of steps.
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Citations
Cites
A Note on the Kinetics of Enzyme Action
Briggs, G. E., & Haldane, J. B. S. (1925) · Biochemical Journal · doi:10.1042/bj0190338 · Cited by 1,327
Receptive fields of cones in the retina of the turtle
Baylor, D. A., Fuortes, M. G. F., & O'Bryan, P. M. (1971) · The Journal of Physiology · doi:10.1113/jphysiol.1971.sp009432 · Cited by 833
Self-citationDark Current and Photocurrent in Retinal Rods
Hagins, W. A., Penn, R. D., & Yoshikami, S. (1970) · Biophysical Journal · doi:10.1016/s0006-3495(70)86308-1 · Cited by 556
Electrical responses of single cones in the retina of the turtle
Baylor, D. A., & Fuortes, M. G. F. (1970) · The Journal of Physiology · doi:10.1113/jphysiol.1970.sp009049 · Cited by 545
Self-citationChanges in time scale and sensitivity in turtle photoreceptors
Baylor, D. A., & Hodgkin, A. L. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010732 · Cited by 533
Self-citationChanges in time scale and sensitivity in the ommatidia of Limulus
Fuortes, M. G. F., & Hodgkin, A. L. (1964) · The Journal of Physiology · doi:10.1113/jphysiol.1964.sp007415 · Cited by 518
Self-citationThe Visual Process: Excitatory Mechanisms in the Primary Receptor Cells
Hagins, W. A. (1972) · Annual Review of Biophysics and Bioengineering · doi:10.1146/annurev.bb.01.060172.001023 · Cited by 480
Detection and resolution of visual stimuli by turtle photoreceptors
Baylor, D. A., & Hodgkin, A. L. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010340 · Cited by 445
Self-citationThe Ferrier Lecture, 1962 Visual adaptation
Rushton, W. A. H. (1965) · Proceedings of the Royal Society of London. Series B. Biological Sciences · doi:10.1098/rspb.1965.0024 · Cited by 352
Kinetics of the Photocurrent of Retinal Rods
Penn, R. D., & Hagins, W. A. (1972) · Biophysical Journal · doi:10.1016/s0006-3495(72)86145-9 · Cited by 331
Cited by
Responses of retinal rods to single photons.
Baylor, D. A., Lamb, T. D., & Yau, K. W. (1979) · The Journal of Physiology · doi:10.1113/jphysiol.1979.sp012716 · Cited by 992
Self-citationEye Smarter than Scientists Believed: Neural Computations in Circuits of the Retina
Gollisch, T., & Meister, M. (2010) · Neuron · doi:10.1016/j.neuron.2009.12.009 · Cited by 795
Visual transduction in cones of the monkey Macaca fascicularis.
Schnapf, J. L., Nunn, B. J., Meister, M., & Baylor, D. A. (1990) · The Journal of Physiology · doi:10.1113/jphysiol.1990.sp018193 · Cited by 478
Self-citationPugh, E. N., & Lamb, T. D. (2000) · Handbook of Biological Physics · doi:10.1016/s1383-8121(00)80008-1 · Cited by 324
Self-citationDistributed Delays Facilitate Amplitude Death of Coupled Oscillators
Atay, F. M. (2003) · Physical Review Letters · doi:10.1103/physrevlett.91.094101 · Cited by 320
Metadata
- Authors
- Baylor, D. A., Hodgkin, A. L., & Lamb, T. D.
- Venue
- The Journal of Physiology
- Publisher
- Wiley
- Published
- 1974-11
- Volume
- 242
- Issue
- 3
- Pages
- 685-727
- ISSN
- 0022-3751 (ISSN-L)
- 1469-7793
- OpenAlex
- W1992818546
- Cited by
- 469
- References
- 16
- FWCI
- 4.38
- Type
- journal article
- Language
- en
- Open access
- green
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