Literature DB >> 2037836

Light adaptation in retinal rods of the rabbit and two other nonprimate mammals.

K Nakatani1, T Tamura, K W Yau.   

Abstract

The responses of rabbit rods to light were studied by drawing a single rod outer segment projecting from a small piece of retina into a glass pipette to record membrane current. The bath solution around the cells was maintained at near 40 degrees C. Light flashes evoked transient outward currents that saturated at up to approximately 20 pA. One absorbed photon produced a response of approximately 0.8 pA at peak. At the rising phase of the flash response, the relation between response amplitude and flash intensity (IF) had the exponential form 1-e-kappa FIF (where kappa F is a constant denoting sensitivity) expected from the absence of light adaptation. At the response peak, however, the amplitude-intensity relation fell slightly below the exponential form. At times after the response peak, the deviation was progressively more substantial. Light steps evoked responses that rose to a transient peak and rapidly relaxed to a lower plateau level. The response-intensity relation again indicated that light adaptation was insignificant at the early rising phase of the response, but became progressively more prominent at the transient peak and the steady plateau of the response. Incremental flashes superposed on a steady light of increasing intensity evoked responses that had a progressively shorter time-to-peak and faster relaxation, another sign of light adaptation. The flash sensitivity changed according to the Weber-Fechner relation (i.e., inversely) with background light intensity. We conclude that rabbit rods adapt to light in a manner similar to rods in cold-blooded vertebrates. Similar observations were made on cattle and rat rods.

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Year:  1991        PMID: 2037836      PMCID: PMC2216483          DOI: 10.1085/jgp.97.3.413

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


  36 in total

1.  Changes in time scale and sensitivity in turtle photoreceptors.

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

2.  Detection and resolution of visual stimuli by turtle photoreceptors.

Authors:  D A Baylor; A L Hodgkin
Journal:  J Physiol       Date:  1973-10       Impact factor: 5.182

3.  Kinetics of the photocurrent of retinal rods.

Authors:  R D Penn; W A Hagins
Journal:  Biophys J       Date:  1972-08       Impact factor: 4.033

4.  Light adaptation in the rat retina: evidence for two receptor mechanisms.

Authors:  D G Green
Journal:  Science       Date:  1971-11-05       Impact factor: 47.728

5.  Incremental responses to light recorded from pigment epithelial cells and horizontal cells of the cat retina.

Authors:  R H Steinberg
Journal:  J Physiol       Date:  1971-08       Impact factor: 5.182

6.  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

7.  Intracellular recordings from gecko photoreceptors during light and dark adaptation.

Authors:  J Kleinschmidt; J E Dowling
Journal:  J Gen Physiol       Date:  1975-11       Impact factor: 4.086

8.  Control of retinal sensitivity. I. Light and dark adaptation of vertebrate rods and cones.

Authors:  R A Normann; F S Werblin
Journal:  J Gen Physiol       Date:  1974-01       Impact factor: 4.086

9.  Regulation of cGMP levels by guanylate cyclase in truncated frog rod outer segments.

Authors:  S Kawamura; M Murakami
Journal:  J Gen Physiol       Date:  1989-10       Impact factor: 4.086

10.  Adaptation in skate photoreceptors.

Authors:  J E Dowling; H Ripps
Journal:  J Gen Physiol       Date:  1972-12       Impact factor: 4.086

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  57 in total

1.  Computational analysis of vertebrate phototransduction: combined quantitative and qualitative modeling of dark- and light-adapted responses in amphibian rods.

Authors:  R D Hamer
Journal:  Vis Neurosci       Date:  2000 Sep-Oct       Impact factor: 3.241

2.  Electroretinographic determination of human rod flash response in vivo.

Authors:  D R Pepperberg; D G Birch; D C Hood
Journal:  Methods Enzymol       Date:  2000       Impact factor: 1.600

3.  Reciprocity between light intensity and rhodopsin concentration across the rat retina.

Authors:  T P Williams; A Squitieri; R P Henderson; J P Webbers
Journal:  J Physiol       Date:  1999-05-01       Impact factor: 5.182

4.  Time course of the flash response of dark- and light-adapted human rod photoreceptors derived from the electroretinogram.

Authors:  C Friedburg; M M Thomas; T D Lamb
Journal:  J Physiol       Date:  2001-07-01       Impact factor: 5.182

5.  Dynamic and steady-state light adaptation of mouse rod photoreceptors in vivo.

Authors:  G A Silva; J R Hetling; D R Pepperberg
Journal:  J Physiol       Date:  2001-07-01       Impact factor: 5.182

6.  Excitation and desensitization of mouse rod photoreceptors in vivo following bright adapting light.

Authors:  Jennifer J Kang Derwent; Nasser M Qtaishat; David R Pepperberg
Journal:  J Physiol       Date:  2002-05-15       Impact factor: 5.182

Review 7.  Speed, sensitivity, and stability of the light response in rod and cone photoreceptors: facts and models.

Authors:  Juan I Korenbrot
Journal:  Prog Retin Eye Res       Date:  2012-05-29       Impact factor: 21.198

8.  Retinal synaptic pathways underlying the response of the rabbit local edge detector.

Authors:  Thomas L Russell; Frank S Werblin
Journal:  J Neurophysiol       Date:  2010-03-24       Impact factor: 2.714

9.  Divergent photic thresholds in the non-image-forming visual system: entrainment, masking and pupillary light reflex.

Authors:  Matthew P Butler; Rae Silver
Journal:  Proc Biol Sci       Date:  2010-09-22       Impact factor: 5.349

10.  Light responses of primate and other mammalian cones.

Authors:  Li-Hui Cao; Dong-Gen Luo; King-Wai Yau
Journal:  Proc Natl Acad Sci U S A       Date:  2014-02-03       Impact factor: 11.205

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