Literature DB >> 11099349

The role of steady phosphodiesterase activity in the kinetics and sensitivity of the light-adapted salamander rod photoresponse.

S Nikonov1, T D Lamb, E N Pugh.   

Abstract

We investigated the kinetics and sensitivity of photocurrent responses of salamander rods, both in darkness and during adaptation to steady backgrounds producing 20-3,000 photoisomerizations per second, using suction pipet recordings. The most intense backgrounds suppressed 80% of the circulating dark current and decreased the flash sensitivity approximately 30-fold. To investigate the underlying transduction mechanism, we expressed the responses as a fraction of the steady level of cGMP-activated current recorded in the background. The fractional responses to flashes of any fixed intensity began rising along a common trajectory, regardless of background intensity. We interpret these invariant initial trajectories to indicate that, at these background intensities, light adaptation does not alter the gain of any of the amplifying steps of phototransduction. For subsaturating flashes of fixed intensity, the fractional responses obtained on backgrounds of different intensity were found to "peel off" from their common initial trajectory in a background-dependent manner: the more intense the background, the earlier the time of peeling off. This behavior is consistent with a background-induced reduction in the effective lifetime of at least one of the three major integrating steps in phototransduction; i.e., an acceleration of one or more of the following: (1) the inactivation of activated rhodopsin (R*); (2) the inactivation of activated phosphodiesterase (E*, representing the complex G(alpha)-PDE of phosphodiesterase with the transducin alpha-subunit); or (3) the hydrolysis of cGMP, with rate constant beta. Our measurements show that, over the range of background intensities we used, beta increased on average to approximately 20 times its dark-adapted value; and our theoretical analysis indicates that this increase in beta is the primary mechanism underlying the measured shortening of time-to-peak of the dim-flash response and the decrease in sensitivity of the fractional response.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11099349      PMCID: PMC2231811          DOI: 10.1085/jgp.116.6.795

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


  38 in total

1.  Responses of retinal rods to single photons.

Authors:  D A Baylor; T D Lamb; K W Yau
Journal:  J Physiol       Date:  1979-03       Impact factor: 5.182

2.  Induction by cyclic GMP of cationic conductance in plasma membrane of retinal rod outer segment.

Authors:  E E Fesenko; S S Kolesnikov; A L Lyubarsky
Journal:  Nature       Date:  1985 Jan 24-30       Impact factor: 49.962

3.  Photoreceptor light adaptation is mediated by cytoplasmic calcium concentration.

Authors:  H R Matthews; R L Murphy; G L Fain; T D Lamb
Journal:  Nature       Date:  1988-07-07       Impact factor: 49.962

4.  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

5.  Regulation of cyclic GMP metabolism in toad photoreceptors. Definition of the metabolic events subserving photoexcited and attenuated states.

Authors:  S M Dawis; R M Graeff; R A Heyman; T F Walseth; N D Goldberg
Journal:  J Biol Chem       Date:  1988-06-25       Impact factor: 5.157

6.  Kinetics and components of the flash photocurrent of isolated retinal rods of the larval salamander, Ambystoma tigrinum.

Authors:  W H Cobbs; E N Pugh
Journal:  J Physiol       Date:  1987-12       Impact factor: 5.182

7.  Magnitude of increase in retinal cGMP metabolic flux determined by 18O incorporation into nucleotide alpha-phosphoryls corresponds with intensity of photic stimulation.

Authors:  N D Goldberg; A A Ames; J E Gander; T F Walseth
Journal:  J Biol Chem       Date:  1983-08-10       Impact factor: 5.157

8.  Control of light-sensitive current in salamander rods.

Authors:  A L Hodgkin; B J Nunn
Journal:  J Physiol       Date:  1988-09       Impact factor: 5.182

9.  Role of calcium in regulating the cyclic GMP cascade of phototransduction in retinal rods.

Authors:  V Torre; H R Matthews; T D Lamb
Journal:  Proc Natl Acad Sci U S A       Date:  1986-09       Impact factor: 11.205

10.  In situ cGMP phosphodiesterase and photoreceptor potential in gecko retina.

Authors:  S Kawamura; M Murakami
Journal:  J Gen Physiol       Date:  1986-05       Impact factor: 4.086

View more
  71 in total

1.  Transduction gain in light adaptation of rod photoreceptors.

Authors:  D R Pepperberg
Journal:  J Gen Physiol       Date:  2001-04       Impact factor: 4.086

2.  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

3.  G-protein betagamma-complex is crucial for efficient signal amplification in vision.

Authors:  Alexander V Kolesnikov; Loryn Rikimaru; Anne K Hennig; Peter D Lukasiewicz; Steven J Fliesler; Victor I Govardovskii; Vladimir J Kefalov; Oleg G Kisselev
Journal:  J Neurosci       Date:  2011-06-01       Impact factor: 6.167

Review 4.  Photoreceptor signaling: supporting vision across a wide range of light intensities.

Authors:  Vadim Y Arshavsky; Marie E Burns
Journal:  J Biol Chem       Date:  2011-11-10       Impact factor: 5.157

Review 5.  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

6.  Phototransduction in primate cones and blowfly photoreceptors: different mechanisms, different algorithms, similar response.

Authors:  J H van Hateren; H P Snippe
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2005-10-25       Impact factor: 1.836

7.  Toward a unified model of vertebrate rod phototransduction.

Authors:  R D Hamer; S C Nicholas; D Tranchina; T D Lamb; J L P Jarvinen
Journal:  Vis Neurosci       Date:  2005 Jul-Aug       Impact factor: 3.241

8.  Light responses and light adaptation in rat retinal rods at different temperatures.

Authors:  S Nymark; H Heikkinen; C Haldin; K Donner; A Koskelainen
Journal:  J Physiol       Date:  2005-07-21       Impact factor: 5.182

9.  Dynamics of mouse rod phototransduction and its sensitivity to variation of key parameters.

Authors:  L Shen; G Caruso; P Bisegna; D Andreucci; V V Gurevich; H E Hamm; E DiBenedetto
Journal:  IET Syst Biol       Date:  2010-01       Impact factor: 1.615

10.  Kinetics of turn-offs of frog rod phototransduction cascade.

Authors:  Luba A Astakhova; Michael L Firsov; Victor I Govardovskii
Journal:  J Gen Physiol       Date:  2008-11       Impact factor: 4.086

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.