Home LiteratureArticle Details
PMID: 650170 Published · ppublish English Journal Article

Ionizable groups and conductances of the rod photoreceptor membrane.

The Journal of general physiology ·Vol. 71 ·No. 3 ·1978-03-00 ·Pages 329-45

Pinto LH, Ostroy SE

Abstract

The ionizable groups and conductances of the rod plasma membrane were studied by measuring membrane potential and input impedance with micropipettes that were placed in the rod outer segments. Reduction of the pH from 8.0 to 6.8 or from 7.8 to 7.3 resulted in membrane depolarization in the dark from 8.0 to 6.8 or from 7.8 to 7.3 resulted in membrane depolarization in the dark (by 2- 3 mV) and an increased size of the light response (also by 2-3 mV). The dark depolarization was accompanied by and increased resting input impedance (by 11-35 Momega). When the pH was decreased in a perfusate in which Cl(-) was replaced by isethionate, the membrane depolarized. When the pH was decreased in a perfusate in which Na(+) was replaced by choline, an increase of input impedance was observed (11-50 Momega) even though a depolarization did not occur. These results are consistent with the interpretation that the effects of decreased extracellular pH result mainly from a decrease in rod membrane K(+) conductance that is presumably cause by protonation of ionizable groups having a pK(a) between 7.3 and 7.8. Furthermore, from these results and results obtained by using CO(2) and NH(3) to affect specifically the internal pH of the cell, it seems unlikely that altered cytoplasmic [H(+)] is a cytoplasmic messenger for excitation of the rod. When the rods were exposed to perfusate in which Na(+) was replaced by choline, the resting (dark) input impedance increased (by 26 Momega +/- 5 Momega SE), and the light-induced changes in input impedance became undetectable. Replacement of Cl(-) by isethionate had no detectable effect on either the resting input impedance or the light-induced changes in input impedance. These results confirm previous findings that the primary effect of light is to decrease the membrane conductance to Na(+) and show that, if any other changes in conductance occur, they depend upon the change in Na(+) conductance. The results are consistent with the following relative resting conductances of the rod membrane: G(Na(+)) similar to G(K(+)) more than 2-5 G(Cl(-)).

MeSH Terms
Ambystoma Animals Anions Binding Sites Bufonidae Cations, Monovalent Membrane Potentials Photoreceptor Cells/physiology
Chemicals
Anions Cations, Monovalent
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Pinto L H
Ostroy S E
References (32)
32 references, click to expand
  1. Acid-base properties of rhodopsin and opsin.
    J Gen Physiol. 1956 Jul 20;39(6):909-22 PMID: 13346044
  2. Effects of injections of calcium and EGTA into the outer segments of retinal rods of Bufo marinus.
    J Physiol. 1977 Aug;269(3):707-22 PMID: 408483
  3. The relation between intercellular coupling and electrical noise in turtle photoreceptors.
    J Physiol. 1976 Dec;263(2):257-86 PMID: 1018249
  4. Rhodopsin and the visual process.
    Biochim Biophys Acta. 1977 Jun 21;463(1):91-125 PMID: 19062
  5. Light-induced resistance changes in retinal rods and cones of the tiger salamander.
    J Physiol. 1974 Jan;236(1):171-91 PMID: 4818491
  6. Ionic mechanism for the photoreceptor potential of the retina of Bufo marinus.
    J Physiol. 1974 Feb;236(3):575-91 PMID: 4207130
  7. Intracellular pH of snail neurones measured with a new pH-sensitive glass mirco-electrode.
    J Physiol. 1974 Apr;238(1):159-80 PMID: 4838803
  8. The electrical response of turtle cones to flashes and steps of light.
    J Physiol. 1974 Nov;242(3):685-727 PMID: 4449052
  9. Dark ionic flux and the effects of light in isolated rod outer segments.
    J Gen Physiol. 1972 Jul;60(1):20-45 PMID: 4537779
  10. Optical measurements of the rapid pH-change in the visual process during the metarhodopsin I-II reaction.
    Z Naturforsch B. 1971 Apr;26(4):352-6 PMID: 4397073
  11. Dark current and photocurrent in retinal rods.
    Biophys J. 1970 May;10(5):380-412 PMID: 5439318
  12. Light-induced resistance changes in single photoreceptors of Necturus and Gekko.
    Vision Res. 1969 Apr;9(4):453-63 PMID: 5822014
  13. Signal transmission along retinal rods and the origin of the electroretinographic a-wave.
    Nature. 1969 Jul 12;223(5202):201-4 PMID: 4307228
  14. The renewal of photoreceptor cell outer segments.
    J Cell Biol. 1967 Apr;33(1):61-72 PMID: 6033942
  15. Functional characteristics of lateral interactions between rods in the retina of the snapping turtle.
    J Physiol. 1976 Jul;259(2):251-82 PMID: 986460
  16. Electrical properties of the rod syncytium in the retina of the turtle.
    J Physiol. 1976 May;257(2):379-406 PMID: 950599
  17. Reconstitution of purple membrane vesicles catalyzing light-driven proton uptake and adenosine triphosphate formation.
    J Biol Chem. 1974 Jan 25;249(2):662-3 PMID: 4272126
  18. Quantum sensitivity of rods in the toad retina.
    Science. 1975 Mar 7;187(4179):838-41 PMID: 1114328
  19. Receptor coupling in the toad retina.
    Cold Spring Harb Symp Quant Biol. 1976;40:547-61 PMID: 820506
  20. Effects of increased intracellular pH-buffering capacity on the light response of Limulus ventral photoreceptor.
    Biochim Biophys Acta. 1976 Jun 4;436(1):140-53 PMID: 6063
  21. Hydrogen ion effects and the vertebrate late receptor potential.
    Biochim Biophys Acta. 1972 Nov 17;283(2):373-80 PMID: 4540875
  22. Hydrogen ion changes of rhodopsin. pK changes and the thermal decay of metarhodopsin II380.
    Arch Biochem Biophys. 1974 Sep;164(1):275-84 PMID: 4473959
  23. Light-induced changes in photoreceptor membrane resistance and potential in Gecko retinas. I. Preparations treated to reduce lateral interactions.
    J Gen Physiol. 1974 Jul;64(1):26-48 PMID: 4837685
  24. Hydrogen ion changes of rhodopsin I. Proton uptake during the metarhodopsin I 478 metarhodopsin II 308 reaction.
    Arch Biochem Biophys. 1973 Jan;154(1):1-7 PMID: 4689776
  25. Chemiosmotic coupling in oxidative and photosynthetic phosphorylation.
    Biol Rev Camb Philos Soc. 1966 Aug;41(3):445-502 PMID: 5329743
  26. [Passive electric properties of a flat cell model].
    Biofizika. 1969 Mar-Apr;14(2):328-35 PMID: 5397659
  27. Hydrogen ion and the activation of electrically excitable membranes.
    Nature. 1969 Nov 8;224(5219):547-9 PMID: 5346594
  28. The light-induced proton uptake in bovine retinal outer segment fragments.
    J Biol Chem. 1968 Nov 25;243(22):5820-6 PMID: 5696620
  29. Effect of external and internal pH changes on K and Cl conductances in the muscle fiber membrane of a giant barnacle.
    J Gen Physiol. 1968 Nov;52(5):773-92 PMID: 5688083
  30. Charges and potentials at the nerve surface. Divalent ions and pH.
    J Gen Physiol. 1968 Feb;51(2):221-36 PMID: 5641636
  31. Protein configuration changes in the photolysis of rhodopsin. I. The thermal decay of cattle lumirhodopsin in vitro.
    Biochim Biophys Acta. 1966 Feb 7;112(2):256-64 PMID: 5942956
  32. Hydrogen ion buffers for biological research.
    Biochemistry. 1966 Feb;5(2):467-77 PMID: 5942950
Article Info
Journal
The Journal of general physiology
Abbr.
J Gen Physiol
ISSN
0022-1295
Published
1978-03-00
Pages
329-45
Language
English
Region
United States
NLM ID
2985110R
PMCID
PMC2215729
Subset
IM
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: product@genelibs.com