The effect of light history on the aspartate-isolated fast-PIII responses of the albino rat retina.

PURPOSE To assess the effect of light-rearing history on the photon-capturing ability, amplitude, and kinetics of the fast-PIII response of the retina. METHODS Albino rats were raised on 12-hour light-12-hour dark cycles, with illumination at 3 lux or 200 lux, and killed at approximately 12 weeks. Retinal rhodopsin content was measured spectrophometrically. The morphology of the rod outer segments (ROS) and the thickness of the outer nuclear layer were determined histologically. Electroretinograms of isolated retinas to 3-microsecond flashes were recorded. The kinetics of fast PIII responses were assessed with a model of the phototransduction cascade. RESULTS Total rhodopsin of 200 lux animals was reduced to 60% that of 3 lux animals: 2.3 +/- 0.2 versus 1.4 +/- 0.1 nmol/eye (mean +/- SD). Length of ROS of 200 lux animals was reduced to 68% of the length of that of 3 lux animals: 20.1 +/- 1.2 versus 13.7 +/- 0.5 microns. The saturated amplitude of fast PIII of 200 lux animals was reduced to 56% that of the 3 lux group: 134 +/- 27 versus 239 +/- 37 microV (T = 22 degrees C). Fast PIII responses of both groups are well described by the kinetic model before slow PIII intrusion (up to 100 ms). Estimated kinetic parameters of the transduction cascade did not differ reliably between the two groups. CONCLUSIONS Diminished saturated amplitude of fast PIII in 200 lux animals is accounted for by the hypothesis that fast PIII is directly proportional to the rod photocurrent and by the finding that the ROS of 200 lux animals are short compared to those of 3 lux animals. Similarity in estimated kinetic parameters of phototransduction suggests that the rods of the two groups differ little in the biochemistry underlying the activation phase of phototransduction.

[1]  E. Pugh,et al.  Recovery phase of the murine rod photoresponse reconstructed from electroretinographic recordings , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[2]  T. Lamb,et al.  Stochastic simulation of activation in the G-protein cascade of phototransduction. , 1994, Biophysical journal.

[3]  D. Hood,et al.  Rod phototransduction in retinitis pigmentosa: estimation and interpretation of parameters derived from the rod a-wave. , 1994, Investigative ophthalmology & visual science.

[4]  A. Cideciyan,et al.  Negative electroretinograms in retinitis pigmentosa. , 1993, Investigative ophthalmology & visual science.

[5]  J. L. Schnapf,et al.  Visual transduction in human rod photoreceptors. , 1993, The Journal of physiology.

[6]  T. Lamb,et al.  Amplification and kinetics of the activation steps in phototransduction. , 1993, Biochimica et biophysica acta.

[7]  E N Pugh,et al.  A quantitative account of the activation steps involved in phototransduction in amphibian photoreceptors. , 1992, The Journal of physiology.

[8]  D. Organisciak,et al.  Adaptive changes in visual cell transduction protein levels: effect of light. , 1991, Experimental eye research.

[9]  D. Farber,et al.  Levels of mRNA encoding proteins of the cGMP cascade as a function of light environment. , 1991, Experimental eye research.

[10]  D. Hood,et al.  A quantitative measure of the electrical activity of human rod photoreceptors using electroretinography , 1990, Visual Neuroscience.

[11]  D. Hood,et al.  The A-wave of the human electroretinogram and rod receptor function. , 1990, Investigative ophthalmology & visual science.

[12]  W. Cobbs,et al.  Kinetics and components of the flash photocurrent of isolated retinal rods of the larval salamander, Ambystoma tigrinum. , 1987, The Journal of physiology.

[13]  R. E. Anderson,et al.  Effect of light history on rod outer-segment membrane composition in the rat. , 1987, Experimental eye research.

[14]  P. O’Brien,et al.  The acylation of rat rhodopsin in vitro and in vivo. , 1986, Experimental eye research.

[15]  T. Williams,et al.  Photostasis: regulation of daily photon-catch by rat retinas in response to various cyclic illuminances. , 1986, Experimental eye research.

[16]  D. Baylor,et al.  The photocurrent, noise and spectral sensitivity of rods of the monkey Macaca fascicularis. , 1984, The Journal of physiology.

[17]  D. M. Eadie,et al.  The effect of detergent selection on retinal outer segment A280/A500 ratios. , 1981, The Journal of biological chemistry.

[18]  D. Baylor,et al.  Responses of retinal rods to single photons. , 1979, The Journal of physiology.

[19]  M. Lavail,et al.  Rhodopsin content and rod outer segment length in albino rat eyes: modification by dark adaptation. , 1978, Experimental eye research.

[20]  W. Noell,et al.  The rod outer segment phospholipid/opsin ratio of rats maintained in darkness or cyclic light. , 1977, Investigative ophthalmology & visual science.

[21]  W. A. Hagins,et al.  Kinetics of the photocurrent of retinal rods. , 1972, Biophysical journal.

[22]  B. S. Winkler,et al.  The electroretinogram of the isolated rat retina. , 1972, Vision research.

[23]  W. A. Hagins,et al.  Dark current and photocurrent in retinal rods. , 1970, Biophysical journal.

[24]  W. Sickel Respiratory and Electrical Responses to Light Stimulation in the Retina of the Frog , 1965, Science.

[25]  K. S. Lashley,et al.  The mechanism of vision. V. The structure and image-forming power of the rat's eye. , 1932 .

[26]  E N Pugh,et al.  Analysis of ERG a-wave amplification and kinetics in terms of the G-protein cascade of phototransduction. , 1994, Investigative ophthalmology & visual science.

[27]  D. Baylor,et al.  Cyclic GMP-activated conductance of retinal photoreceptor cells. , 1989, Annual review of neuroscience.

[28]  I. Hanawa,et al.  The slow P III response of the isolated frog retina. , 1978, The Japanese journal of physiology.

[29]  M. Murakami,et al.  The early and late receptor potentials of monkey cones and rods. , 1965, Cold Spring Harbor symposia on quantitative biology.