Literature DB >> 5315587

Rhodopsin and porphyropsin fields in the adult bullfrog retina.

T E Reuter, R H White, G Wald.   

Abstract

Though it had been supposed earlier that the bullfrog undergoes a virtually complete metamorphosis of visual systems from vitamin A(2) and porphyropsin in the tadpole to vitamin A(1) and rhodopsin in the adult, the present observations show that the retina of the adult frog may contain as much as 30-40% porphyropsin, all of it segregated in the dorsal zone. The most dorsal quarter of the adult retina may contain 81-89% porphyropsin mixed with a minor amount of rhodopsin; the ventral half contains only rhodopsin. Further, the dorsal zone contains a two to three times higher concentration of visual pigments than the ventral retina. The pigment epithelium underlying the retina contains a corresponding distribution of vitamins A(1) and A(2), predominantly vitamin A(2) in the dorsal pigment epithelium, exclusively vitamin A(1) in the ventral zone. The retina accepts whatever vitamin A the pigment epithelium provides it with, and turns it into the corresponding visual pigment. Thus, a piece of light-adapted dorsal retina laid back on ventral pigment epithelium regenerates rhodopsin, whereas a piece of light-adapted ventral retina laid back on dorsal pigment epithelium regenerates predominantly porphyropsin. Vitamin A(2) must be made from vitamin A(1), by dehydrogenation at the 3,4-bond in the ring. This conversion must occur in the pigment epithelium, presumably through the action of a vitamin A-3,4-dehydrogenase. The essential change at metamorphosis is to make much less of this dehydrogenase, and to sequester it in the dorsal pigment epithelium. Some adult bullfrogs, perhaps characteristically taken in the summer, contain very little porphyropsin-only perhaps 5%-still sequestered in the dorsal retina. The gradient of light over the retinal surface has little if any effect on this distribution. The greater density of visual pigments in the dorsal retina, and perhaps also-although this is less clear-the presence of porphyropsin in this zone, has some ecological importance in increasing the retinal sensitivity to the dimmer and, on occasion, redder light received from below.

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Year:  1971        PMID: 5315587      PMCID: PMC2226032          DOI: 10.1085/jgp.58.4.351

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


  32 in total

1.  Molecular basis of visual excitation.

Authors:  G Wald
Journal:  Science       Date:  1968-10-11       Impact factor: 47.728

2.  Visual pigments of frog and tadpole (Rana pipiens).

Authors:  P A Liebman; G Entine
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3.  The visual pigment of the green rods.

Authors:  H J Dartnall
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4.  The visual pigments of freshwater fishes.

Authors:  S A Schwanzara
Journal:  Vision Res       Date:  1967-03       Impact factor: 1.886

5.  Spectroscopic properties of porphyropsins.

Authors:  C D Bridges
Journal:  Vision Res       Date:  1967-05       Impact factor: 1.886

6.  Absorption properties, interconversions, and environmental adaptation of pigments from fish photoreceptors.

Authors:  C D Bridges
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1965

7.  A critical analysis of the visual pigments of salmon and trout.

Authors:  F W Munz; D D Beatty
Journal:  Vision Res       Date:  1965-01       Impact factor: 1.886

8.  Visual pigments in a fish exposed to different light-environments.

Authors:  C D Bridges
Journal:  Nature       Date:  1965-06-12       Impact factor: 49.962

9.  The spectral clustering of visual pigments.

Authors:  H J Dartnall; J N Lythgoe
Journal:  Vision Res       Date:  1965-04       Impact factor: 1.886

10.  Visual pigments and spectral sensitivity in Rana temporaria and other European tadpoles.

Authors:  W R Muntz; T Reuter
Journal:  Vision Res       Date:  1966-12       Impact factor: 1.886

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  23 in total

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Authors:  Petri Ala-Laurila; Kristian Donner; Ari Koskelainen
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2.  The frequency of isomerization-like 'dark' events in rhodopsin and porphyropsin rods of the bull-frog retina.

Authors:  K Donner; M L Firsov; V I Govardovskii
Journal:  J Physiol       Date:  1990-09       Impact factor: 5.182

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5.  Two temporal phases of light adaptation in retinal rods.

Authors:  Peter D Calvert; Victor I Govardovskii; Vadim Y Arshavsky; Clint L Makino
Journal:  J Gen Physiol       Date:  2002-02       Impact factor: 4.086

6.  Seasonal cycle in vitamin A1/A2-based visual pigment composition during the life history of coho salmon (Oncorhynchus kisutch).

Authors:  S E Temple; E M Plate; S Ramsden; T J Haimberger; W-M Roth; C W Hawryshyn
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7.  Transduction heats in retinal rods: tests of the role of cGMP by pyroelectric calorimetry.

Authors:  W A Hagins; P D Ross; R L Tate; S Yoshikami
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8.  Ganglion cell performance at absolute threshold in toad retina: effects of dark events in rods.

Authors:  D R Copenhagen; K Donner; T Reuter
Journal:  J Physiol       Date:  1987-12       Impact factor: 5.182

9.  Effects of adapting lights on the time course of the receptor potential of the anuran retinal rod.

Authors:  J A Coles; S Yamane
Journal:  J Physiol       Date:  1975-05       Impact factor: 5.182

10.  Competition between retinol and 3,4-didehydroretinol for esterification in crude pigment epithelial cell fractions.

Authors:  A T Tsin
Journal:  Experientia       Date:  1986-08-15
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