Literature DB >> 650170

Ionizable groups and conductances of the rod photoreceptor membrane.

L H Pinto, S E Ostroy.   

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(-)).

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Year:  1978        PMID: 650170      PMCID: PMC2215729          DOI: 10.1085/jgp.71.3.329

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  32 in total

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Authors:  S E Ostroy
Journal:  Biochim Biophys Acta       Date:  1977-06-21

2.  The relation between intercellular coupling and electrical noise in turtle photoreceptors.

Authors:  T D Lamb; E J Simon
Journal:  J Physiol       Date:  1976-12       Impact factor: 5.182

3.  Optical measurements of the rapid pH-change in the visual process during the metarhodopsin I-II reaction.

Authors:  H M Emrich
Journal:  Z Naturforsch B       Date:  1971-04       Impact factor: 1.047

4.  The electrical response of turtle cones to flashes and steps of light.

Authors:  D A Baylor; A L Hodgkin; T D Lamb
Journal:  J Physiol       Date:  1974-11       Impact factor: 5.182

5.  Dark ionic flux and the effects of light in isolated rod outer segments.

Authors:  J I Korenbrot; R A Cone
Journal:  J Gen Physiol       Date:  1972-07       Impact factor: 4.086

6.  Light-induced resistance changes in retinal rods and cones of the tiger salamander.

Authors:  A Lasansky; P L Marchiafava
Journal:  J Physiol       Date:  1974-01       Impact factor: 5.182

7.  Ionic mechanism for the photoreceptor potential of the retina of Bufo marinus.

Authors:  J E Brown; L H Pinto
Journal:  J Physiol       Date:  1974-02       Impact factor: 5.182

8.  Intracellular pH of snail neurones measured with a new pH-sensitive glass mirco-electrode.

Authors:  R C Thomas
Journal:  J Physiol       Date:  1974-04       Impact factor: 5.182

9.  Effects of injections of calcium and EGTA into the outer segments of retinal rods of Bufo marinus.

Authors:  J E Brown; J A Coles; L H Pinto
Journal:  J Physiol       Date:  1977-08       Impact factor: 5.182

10.  Acid-base properties of rhodopsin and opsin.

Authors:  C M RADDING; G WALD
Journal:  J Gen Physiol       Date:  1956-07-20       Impact factor: 4.086

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  6 in total

1.  Protons suppress the dark current of frog retinal rods.

Authors:  P A Liebman; P Mueller; E N Pugh
Journal:  J Physiol       Date:  1984-02       Impact factor: 5.182

2.  Effects of changing external potassium and chloride concentrations on the photoresponses of Bufo bufo rods.

Authors:  M Capovilla; L Cervetto; V Torre
Journal:  J Physiol       Date:  1980-10       Impact factor: 5.182

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

Authors:  B L Bastian; G L Fain
Journal:  J Physiol       Date:  1982-09       Impact factor: 5.182

4.  Light-induced proton permeability changes in retinal rod photoreceptor disk membranes.

Authors:  H G Smith; R S Fager
Journal:  Biophys J       Date:  1991-02       Impact factor: 4.033

5.  Modulation of membrane conductance in rods of Bufo marinus by intracellular calcium ion.

Authors:  B Oakley; L H Pinto
Journal:  J Physiol       Date:  1983-06       Impact factor: 5.182

6.  Light induced changes of internal pH in a barnacle photoreceptor and the effect of internal pH on the receptor potential.

Authors:  H M Brown; R W Meech
Journal:  J Physiol       Date:  1979-12       Impact factor: 5.182

  6 in total

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