Abstract
Changes in the steady state level of retinols, retinaldehydes and retinyl esters in the trans and 11-cis forms and trans retinoic acid were measured in whole chicken eye during development from day 6in ovo to day 3 post-hatch. These retinoids, quantified by different HPLC systems, were detected in this time sequence: trans-retinol and trans-retinyl esters in the first weekin ovo, 11-cis-retinol in the second week. The highest level of 11-cis-retinaldehyde and 11-cis-retinyl esters was reached at the end of developmentin ovo; however, their levels increased further after hatching. The retinoic acid level decreased at the end of the first week, rising again at the end of the second week.
The enzyme activities involved in the metabolism of these retinoids-acyl-CoA: retinol acyltransferase, trans-retinol dehydrogenase, 11-cis-retinol dehydrogenase, trans-retinyl ester hydrolase and trans: 11-cis-retinol isomerase were also estimated and they were detectable already in the first week of developmentin ovo.
At day 6 of the biosynthesis of retinoic acid by the retinaldehyde dehydrogenase activity from retina cytosol was also shown.
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Zimmerman WF: The distribution and proportions of vitamin A compounds during the visual cycle in the rat. Vision Res 14: 795–802 1974
Hubbard R, Dowling JE: Formation and utilization of 11-cis vitamin A by the eye tissues during light and dark adaptation. Nature 193: 341–343, 1962
Bridges CDB: Storage, distribution and utilization of vitamin A in the eyes of adult amphibians and their tadpoles. Vision Res 15: 1311–1323, 1975
Carter-Dawson L, Alvarez RA, Fong SL, Liou GI, Sperling HG, Bridges CDB: Rhodopsin, 11-cis vitamin A, and interstitial retinol-binding protein (IRBP) during development in normal and rd mutant mice. Devel Biol 116: 431–438, 1986
Wiggert B, Masterson E, Coulombre AJ: Changes in retinoid binding levels during development of the chicken cornea. Exp Eye Res 37: 499–505, 1983
Groenendijk GWT, De Grip WJ, Daemen FJM: Quantitative determination of retinals with complete retention of their geometric configuration. Biochim Biophys Acta 617: 430–438, 1980
Ong DE, Chytil F: Cellular retinoic acid-binding protein from rat testis-purification and characterization. J Biol Chem 253: 4551–4554, 1978
Bridges CDB, Alvarez RA: Measurement of the vitamin A cycle. Methods Enzymol 81: 463–485, 1982
Hubbard R, Brown PK, Bownds D: Methodology of vitamin A and visual pigments. Methods Enzymol 18: 615–653, 1971
Futterman S, Rollins MH: The catalytic isomerization of all-transretinal to 9-cis-retinal and 13-cis-retinal. J Biol Chem 248: 7773–7779, 1973
Landers GM, Olson JA: Statistical solvent optimization for the separation of geometric isomers of retinol by high-performance liquid chromatography. J Chromat 291: 51–57, 1984
Groenendijk GWT, Jansen PAA, Bonting SL, Daemen FJM: Analysis of geometrically isomeric vitamin A compounds. Methods Enzymol 67: 203–220, 1980
Gueli MC, Nicotra CMA, Pintaudi AM, Paganini A, Pandolfo L, De Leo G, Di Bella MA: Retinyl ester hydrolases in retinal pigment epithelium. Arch Biochem Biophys 288: 572–577, 1991
Lowry OH, Rosebrough NJ, Farr AL, Randall RJ: Protein measurement with the Folin phenol reagent. J Biol Chem 193: 265–275, 1951
Stroeva OG, Mitashov VI: Retinal pigment epithelium: proliferation and differentiation during development and regeneration. Intern Rev Cytol 83: 221–291, 1983
Frickel F: Chemistry and physical properties of retinoids. In: MB Sporn, AB Roberts, DS Goodman (eds) The Retinoids, Vol. I. Academic Press, New York, 1984, pp 7–145
Rando RR, Chang A: Studies on the catalyzed interconversions of vitamin A derivatives. J Am Chem Soc 105: 2879–2882, 1983
Goodman DS, Huang HS: Biosynthesis of vitamin A with rat intestinal enzymes. Science 149: 879–880, 1965
Olson JA, Hayaishi O: The enzymatic cleavage of beta carotene into vitamin A by soluble enzymes of rat liver and intestine. Proc Natl Acad Sci USA 54: 1364–1369, 1965
Wolken JJ: The vertebrate visual pigments. In: JJ Wolken (ed.) Photoprocesses, photoreceptors and evolution. Academic Press, New York, 1975, pp 195–211
Hansen S, Maret W: Retinal is not formedin vitro by enzymatic central cleavage of B-carotene. Biochemistry 27: 200–206, 1988
Olson JA: Provitamin A function of carotenoids: the conversion of B-carotene into vitamin A. J Nutr 119: 105–108, 1989
Bowmaker JK, Knowles A: The visual pigments and oil droplets of the chicken retina. Vision Res 17: 755–764, 1977
Fager LY, Fager RS: Chicken blue and chicken violet, short wavelength sensitive visual pigments. Vision Res 21: 581–586, 1981
Schiedt K: New aspects of carotenoid metabolism in animals. In: NI Krinski, MM Mathews-Roth, RF Taylor (eds) Carotenoids: chemistry and biology. Plenum Press, New York, 1989, pp 247–268
Rodriguez KA, Tsin ATC: Retinyl esters in the vertebrate neuroretina. Am J Physiol 25: R255-R258, 1989
Bridges CDB, Alvarez RA, Fong SL, Liou GI, Ulshafer RJ: Rhodopsin, vitamin A, and interstitial retinoid-binding protein in the rd chicken. Invest Ophthalmol Vis Sci 28: 613–617, 1987
Saari JC, Bredberg DL: Lecithin: retinol acyltransferase in retinal pigment epithelium microsomes. J Biol Chem 264: 8636–8640, 1989
Ubels JL, Huebler SM: Esterification of retinol in lacrimal gland —evidence for acyl-CoA: retinol acyltransferase activity. Invest Ophthalmol Vis Sci 31: 582–589, 1990
Bernstein PS, Law WC, Rando RR: Isomerization of all-trans-retinoids to 11-cis-retinoidsin vitro. Proc Natl Acad Sci USA 84: 1849–1853, 1987
Deigner PS, Law WC, Canada FJ, Rando RR: Membranes as the energy source in the endergonic transformation of vitamin A to 11-cis-retinol. Science 244: 968–971, 1989
Rando RR: Membrane phospholipids as an energy source in the operation of the visual cycle. Biochemistry 30: 595–602, 1991
Bridges CDB: Retinoids in photosensitive systems. In: MB Sporn, AB Roberts, DS Goodman (eds) The Retinoids, Vol. 2. Academic Press, New York, 1984, pp 125–176
Plantner JJ, Lentrichia BB, Kean EL: Biogenesis and content of rhodopsin in the retina of the chick during development. Curr Eye Res 7: 503–510, 1988
Kahn AJ: An autoradiographic analysis of the time of appearance of neurons in the developing chick neural retina. Devel Biol 38: 30–40, 1974
Wiggert B, Bergsma DR, Helmsen R, Chader GJ: Vitamin A receptors. Retinoic acid binding in ocular tissues. Biochem J 169: 87–94, 1978
Wiggert B, Masterson E, Israel P, Chader GJ: Differential retinoid binding in chick pigment epithelium and choroid. Invest Ophthalmol Visual Sci 18: 306–310, 1979
Degenstein L, Moscona AA: Retinoic acid inhibits conversion of dissociated Müller glia into lens-like cells. Exp Eye Res 43: 93–102, 1986
Gaur VP, De Leeuw AM, Milam AH, Saari JC: Localization of cellular retinoic acid-binding protein to amacrine cells of rat retina. Exp Eye Res 50: 505–511, 1990
Hinds JW, Hinds PL: Early development of amacrine cells in the mouse retina: an electron microscopic, serial section analysis. J Comp Neur 179: 277–300, 1978
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Nicotra, C.M.A., Gueli, M.C., De Luca, G. et al. Retinoid dynamics in chicken eye during pre-and postnatal development. Mol Cell Biochem 132, 45–55 (1994). https://doi.org/10.1007/BF00925674
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DOI: https://doi.org/10.1007/BF00925674