bioactive additives, carotenoids, retinoids, shrimp

Authors

  • J. Paniagua-Michel CICESE-Department of Marine Biotechnology
  • M. Liñan-Cabello CICESE-Department of Marine Biotechnology

Keywords:

bioactive additives, carotenoids, retinoids, shrimp

Abstract

Additional efforts need to be devoted to understanding of the bioactive forms of non-produced
de novo metabolites such as carotenoids and their derived metabolites, retinoids in crustaceans. Dietary
carotenoids are the sole biological precursos of retinoids in animal systems. The results obtained in survival,
gonadosomatic and hepatosomatic index in treatments with carotenoids and retinol, demonstrated the
importance of carotenoids to yield retinal and retinol needed for significicantly better gonad development. A
rough correlation exists between the rate of retinal formation and the biological activity of the administered
carotenoids. The presence of 9-cis and 13-cis retinol in reproductive tissue of P. vannamei shrimp points-out
their role in the RXR receptors due to the previously reported function of these isomers in the binding
domains fo genes which induces growth and development by controlling the production of local morphogenic
signals by a nuclear receptor signaling pathway.

Downloads

Download data is not yet available.

References

Alava, V.R., Kanazawa, A., Teshima, S., Koshio, S., 1993. Effects of dietary vitamins A, E, and C on the ovarian

development of Penaeus japonicus, Nippon Sussian Gakkaishi, 59: 235-242.

Brody, T., 1999. Nutritional Biochemistry. Academic Press. New York. 1000pp.

Duester, G., 1996. Involvement of alcohol dehydrogenase, short-chain dehydrogenase/reductase, and cytochrome p450 in

the control of retinoid signaling by activation of retinoic acid synthesis. Biochemistry, 35: 12221-12227.

Durica, D., Chung, A., Hopkins, P., 1999. Characterization of EcR and RXR gene homologs and receptor expression

during the molt cycle in the crab, Uca pugilator. Amer. Zool. 39: 758-773.

Lakshman, M.R., Johnson, L.H., Okoh, C., Attlesey, M., Mydhkorsky, I., 1993. Conversion of all trans ß-carotene to retinal

by an enzyme from the intestinal mucosa of human neonates. J. Nutr. Biochem. 4: 659-663.

Mangelsdorf, D.J., Borgmeyer, U., Heyman, R.A., Zhou, J.Y., Ong, E.S., Oro, A.E., Evans, R.M., 1995. Characterization of

three RXR genes that mediate the action of 9-cis retinoic acid. Genes Dev. 6:329-344.

Meyers, S. P., Latscha, T., 1997. Carotenoids. In advances in world aquaculture. Vo.6. Crustacean Nutrition. World

Aquaculture Society.

Napoli, J.L., Horst, R.L., 1989. Quantitative analysis of naturally occurring retinoids. In: Redfern, Ch. (ed). Retinoid

protocols. Humana Press. New Jersey.

Petkovich, M., 1992. Regulation of gene expression by vitamin a: The role of nuclear retinoic acid receptors. Ann. Rev.

Nutr. 12: 443-471.

Schiedt, K., Bishop, S. Glinz, E., 1993. Recent progress on carotenoid metabolism in animals. Pure and App. Chem. 63: 89-

Takeuchi, T., Dedi, J., Haga Y., Seikai, T., Watanabe, T. 1998. Effect of vitamin A compounds on bone deformity in larval

Japanese flounder (Paralichthys olivaceus). Aquaculture, 169: 155-165.

Wolf, G. 1990. Recent Progres in vitamin A research: nuclear retinoic acid receptors and their interactions with gene

elements. J. Nutr. Biochem. 1: 284-289.

Downloads

How to Cite

Paniagua-Michel, J., & Liñan-Cabello, M. (2019). bioactive additives, carotenoids, retinoids, shrimp. Avances En Nutrición Acuicola. Retrieved from https://nutricionacuicola.uanl.mx/index.php/acu/article/view/281

Similar Articles

<< < 3 4 5 6 7 8 9 10 > >> 

You may also start an advanced similarity search for this article.