Hostname: page-component-cd9895bd7-7cvxr Total loading time: 0 Render date: 2024-12-18T13:57:38.263Z Has data issue: false hasContentIssue false

Recovery from bleaching in photoreceptors promoted by biotin, pyruvate, and glucose

Published online by Cambridge University Press:  02 June 2009

K.N. Leibovic
Affiliation:
State University of New York at Buffalo, Department of Biophysical Sciences, Buffalo
J. Bandarchi
Affiliation:
State University of New York at Buffalo, Department of Biophysical Sciences, Buffalo

Abstract

In the rods of Bufo marinus and other species, bleaching of the rhodopsin in isolated cells leads to a loss of sensitivity and response amplitude and to a shortened response duration. These changes are permanent for cells bathed in Ringer&s solution. They are due to as yet unknown modulations in the transduction biochemistry. In this paper, we report that these changes can be partly or completely reversed by supplying biotin, pyruvate, and elevated glucose to the rod. The time course of this reversal and the substances which promote it imply that these are metabolically mediated effects. Based on the reported action of biotin and pyruvate on the one hand and on the changes of the response waveforms on the other hand, we believe that the phenomena we observe involve the later steps of the transduction cycle.

Type
Short Communication
Copyright
Copyright © Cambridge University Press 1990

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Azuma, K., Azuma, M. & Sickel, W. (1977). Regeneration of rhodopsin in frog rod outer segments. Journal of Physiology 271, 747759.CrossRefGoogle ScholarPubMed
Clack, J.W., OakleyII, B. II, B. & Pepperberg, D.R. (1982). Light-dependent effects of a hydrolysis-resistant analog of GTP on rod photoresponses in the toad retina. Proceedings of the National Academy of Sciences of the U.S.A. 79, 26902694.CrossRefGoogle ScholarPubMed
Cocozza, J.D. & Ostroy, S.E. (1987). Factors affecting the regeneration of rhodopsin in the isolated amphibian retina. Vision Research 27, 10851091.CrossRefGoogle ScholarPubMed
Cornwall, M.C., Fein, A. & MacNichol, E.F. (1983). Spatial localization of bleaching adaptation in isolated rod photoreceptors. Proceedings of the National Academy of Sciences of the U.S.A. 80, 27852788.CrossRefGoogle Scholar
Donner, K.O. & Hemila, S. (1975). Kinetics of long-lived rhodopsin in frog rod outer segments. Vision Research 15, 985995.CrossRefGoogle Scholar
Dowling, J.E. & Ripps, H. (1972). Adaptation in skate photoreceptors. Journal of General Physiology 60, 698719.CrossRefGoogle ScholarPubMed
Fesenko, E.E., Kolesnikov, S.S. & Lyubarski, A.L. (1985). Induction by cGMP of cationic conductance in plasma membrane of rod outer segments. Nature 313, 310313.CrossRefGoogle Scholar
Lamb, T.D. & Matthews, H.R. (1988). Incorporation of analogs of GTP and GDP into rod photoreceptors isolated from the tiger salamander. Journal of Physiology 407, 463489.CrossRefGoogle ScholarPubMed
Leibovic, K.N. (1983). Bleaching of the isolated retina. Biological Cybernetics 48, 109114.CrossRefGoogle ScholarPubMed
Leibovic, K.N. (1986). A new method of nonenzymatic dissociation of the Bufo retina. Journal of Neuroscience Methods 15, 301306.CrossRefGoogle ScholarPubMed
Leibovic, K.N., Dowling, J.E. & Kim, Y.Y. (1987). Background and bleaching equivalence in steady-state adaptation of vertebrate rods. Journal of Neuroscience 7(4), 10561063.CrossRefGoogle ScholarPubMed
Matthews, H.R., Murphy, R.L.W., Fain, G.L. & Lamb, T.D. (1988). Photoreceptor light adaptation is mediated by cytoplasmic calcium concentration. Nature 334, 6769.CrossRefGoogle ScholarPubMed
Nakatani, K. & Yau, K.-W. (1988). Calcium and light adaptation in retinal rods and cones. Nature 334, 6971.CrossRefGoogle ScholarPubMed
Normann, R.A. & Werblin, F.S. (1974). Control of retinal sensitivity, I: Light and dark adaptation of vertebrate rods and cones. Journal of General Physiology 63, 3761.CrossRefGoogle ScholarPubMed
Pepperberg, D.R., Brown, P.K., Lurie, M. & Dowling, J.E. (1978). Visual pigment and photoreceptor sensitivity in the isolated skate retina. Journal of General Physiology 71, 369396.CrossRefGoogle ScholarPubMed
Pugh, E.N. & Cobbs, W.H. (1986). Visual transduction in vertebrate rods and cones. Vision Research 26(10), 16131643.CrossRefGoogle ScholarPubMed
Stryer, L. (1986). Cyclic GMP cascade of vision. Annual Review of Neuroscience 9, 87119.CrossRefGoogle ScholarPubMed
Torre, V., Matthews, H.R. & Lamb, T.D. (1986). Role of calcium in regulating the cGMP cascade of phototransduction in retinal rods. Proceedings of the National Academy of Sciences of the U.S.A. 83, 71097113.CrossRefGoogle ScholarPubMed
Vesely, D.L. (1982). Biotin enhances guanylate cyclase activity. Science 216, 13291330.CrossRefGoogle ScholarPubMed
Weinstein, G.W., Hobson, R.R. & Dowling, J.E. (1976). Light and dark adaptation in isolated rat retina. Nature 215, 134138.CrossRefGoogle Scholar
Yau, K.-W. & Nakatani, K. (1985). Light-suppressible cyclic GMP-sensitive conductance in the plasma membrane of a truncated rod outer segment. Nature 317, 252255.CrossRefGoogle ScholarPubMed