Home LiteratureArticle Details
PMID: 6816919 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

The effects of low calcium and background light on the sensitivity of toad rods.

The Journal of physiology ·Vol. 330 ·1982-09-00 ·Pages 307-29

Bastian BL, Fain GL

Abstract

1. We have examined the effects of decreases in extracellular Ca(2+) concentration on the intracellularly recorded light responses of rods from the toad, Bufo marinus. In agreement with previous results (Brown & Pinto, 1974; Lipton, Ostroy & Dowling, 1977), Ca(2+) concentrations below 10(-6) M produced a depolarization of rod resting membrane potential of approximately 30-40 mV and a corresponding increase in the maximum amplitude of the rod's light responses, so that saturating flashes in normal and low Ca(2+) Ringer produced hyperpolarizations to approximately the same membrane potential.2. The rod's sensitivity was reduced in low Ca(2+) Ringer by an amount dependent upon the extracellular Ca(2+) concentration. At 10(-6) M-Ca(2+), sensitivity was approximately 0.6 log units below normal. Thereafter, it dropped nearly linearly with [Ca(2+)](o) to a value approximately 4.0 log units below normal at 10(-9) M-Ca(2+). Most of the decline occurred within 1-2 min after the solution change as the membrane potential depolarized, but sensitivity continued to fall slowly with time at the lowest Ca(2+) concentrations. Exposure to low Ca(2+) solutions altered the kinetics of the receptor response to brief flashes, delaying response onset and time-to-peak but affecting the time course of decay very little.3. The sensitivity of the rod to maintained steps of light was also reduced in low Ca(2+). Furthermore, the changes in sensitivity produced by background illumination were very much smaller in low Ca(2+) than in normal Ringer. In some cases backgrounds actually increased sensitivity.4. In 10(-8) M-Ca(2+), backgrounds which themselves produced no response in the rod and no changes in rod sensitivity produced large decreases in response latency for responses of all amplitudes, and pronounced changes in time-to-peak and time-to-decay for moderate and large amplitude responses.5. Since the effects of background light and low Ca(2+) on the wave form of the rod are distinct and in some cases antagonistic, and since the changes in receptor sensitivity produced by backgrounds and low Ca(2+) are not additive, the decreases in sensitivity produced by exposure to low Ca(2+) appear to be caused by a mechanism distinct from normal light adaptation. We suggest that they are caused by an increase in the buffering capacity of the receptor cytosol for Ca(2+) and that Ca(2+) is the excitatory messenger or ;internal transmitter', as originally suggested by Yoshikami & Hagins (1971).

MeSH Terms
Adaptation, Ocular Animals Bufo marinus Calcium/physiology Light Membrane Potentials/drug effects Photic Stimulation Photoreceptor Cells/physiology
Chemicals
Calcium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Bastian B L
Fain G L
References (31)
31 references, click to expand
  1. 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):701-19 PMID: 5025746
  2. Transport and metabolism of calcium ions in nerve.
    Prog Biophys Mol Biol. 1972;24:177-223 PMID: 4118937
  3. Ionic mechanism for the photoreceptor potential of the retina of Bufo marinus.
    J Physiol. 1974 Feb;236(3):575-91 PMID: 4207130
  4. Proceedings: A role for Ca2+ in excitation of retinal rods and cones.
    Exp Eye Res. 1974 Mar;18(3):299-305 PMID: 4833765
  5. Changes in time scale and sensitivity in turtle photoreceptors.
    J Physiol. 1974 Nov;242(3):729-58 PMID: 4449053
  6. Reconstruction of the electrical responses of turtle cones to flashes and steps of light.
    J Physiol. 1974 Nov;242(3):759-91 PMID: 4449054
  7. Quantum sensitivity of rods in the toad retina.
    Science. 1975 Mar 7;187(4179):838-41 PMID: 1114328
  8. Effects of adapting lights on the time course of the receptor potential of the anuran retinal rod.
    J Physiol. 1975 May;247(1):189-207 PMID: 805837
  9. Ionic aspects of excitation in rod outer segments.
    Ciba Found Symp. 1975;(31):169-89 PMID: 1080099
  10. Intracellular recordings from gecko photoreceptors during light and dark adaptation.
    J Gen Physiol. 1975 Nov;66(5):617-48 PMID: 1194887
  11. A possible model for the electrical responses of frog rods during light and dark adaptation.
    Biol Cybern. 1976 Aug 30;23(4):229-39 PMID: 963128
  12. Sensitivity of toad rods: Dependence on wave-length and background illumination.
    J Physiol. 1976 Sep;261(1):71-101 PMID: 825637
  13. Calcium content of frog rod outer segments and discs.
    Biochim Biophys Acta. 1977 Jul 14;468(2):194-208 PMID: 884086
  14. Electrical and adaptive properties of rod photoreceptors in Bufo marinus. I. Effects of altered extracellular Ca2+ levels.
    J Gen Physiol. 1977 Dec;70(6):747-70 PMID: 412914
  15. Actions of EGTA and high calcium on the cones in the turtle retina.
    J Physiol. 1978 Feb;275:419-37 PMID: 416204
  16. Ionizable groups and conductances of the rod photoreceptor membrane.
    J Gen Physiol. 1978 Mar;71(3):329-45 PMID: 650170
  17. Ionic blockage of the light-regulated sodium channels in isolated rod outer segments.
    J Gen Physiol. 1978 Jun;71(6):657-81 PMID: 27574
  18. The membrane current of single rod outer segments.
    J Physiol. 1979 Mar;288:589-611 PMID: 112242
  19. Calcium translocation and storage of isolated intact cattle rod outer segments in darkness.
    Biochim Biophys Acta. 1979 Jul 5;554(2):441-59 PMID: 114221
  20. Spread of activation and desensitisation in rod outer segments.
    Nature. 1980 Jan 3;283(5742):85-7 PMID: 7350530
  21. Light adaptation in toad rods: requirement for an internal messenger which is not calcium.
    J Physiol. 1979 Dec;297(0):493-520 PMID: 119846
  22. Ion selectivity of the cation transport system of isolated intact cattle rod outer segments: evidence for a direct communication between the rod plasma membrane and the rod disk membranes.
    Biochim Biophys Acta. 1980 May 8;598(1):66-90 PMID: 7417431
  23. Calcium flux across disk membranes. Studies with intact rod photoreceptors and purified disks.
    J Gen Physiol. 1980 Sep;76(3):253-86 PMID: 6252276
  24. Measuring calcium uptake and release by invertebrate photoreceptor cells by laser microprobe mass spectroscopy.
    Scan Electron Microsc. 1980;(Pt 2):647-54, 606 PMID: 7423134
  25. Calcium spikes in toad rods.
    J Physiol. 1980 Jun;303:495-513 PMID: 6776262
  26. Control of the cyclic GMP phosphodiesterase of frog photoreceptor membranes.
    J Gen Physiol. 1980 Nov;76(5):631-45 PMID: 6255064
  27. Biochemical steps in visual transduction: roles for nucleotides and calcium ions.
    Photochem Photobiol. 1980 Oct;32(4):487-90 PMID: 6256785
  28. Effects of changing external potassium and chloride concentrations on the photoresponses of Bufo bufo rods.
    J Physiol. 1980 Oct;307:529-51 PMID: 6782240
  29. Membrane conductances of photoreceptors.
    Prog Biophys Mol Biol. 1981;37(2):91-147 PMID: 6264547
  30. Effect of ions on the light-sensitive current in retinal rods.
    Nature. 1981 Aug 6;292(5823):502-5 PMID: 6265800
  31. CHANGES IN TIME SCALE AND SENSITIVITY IN THE OMMATIDIA OF LIMULUS.
    J Physiol. 1964 Aug;172:239-63 PMID: 14205019
Article Info
Journal
The Journal of physiology
Abbr.
J Physiol
ISSN
0022-3751
Published
1982-09-00
Pages
307-29
Language
English
Region
England
NLM ID
0266262
PMCID
PMC1225300
Subset
IM
Grants
NEI NIH HHS · EY 00331 · United States
NEI NIH HHS · EY 02728 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]