Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-26T08:20:00.374Z Has data issue: false hasContentIssue false

Effect of nature of dietary lipids on European sea bass morphogenesis: implication of retinoid receptors

Published online by Cambridge University Press:  08 March 2007

Laure Villeneuve*
Affiliation:
UMR1067, Nutrition Aquaculture Génomique, IFREMER, 29280 Plouzané, France
Enric Gisbert
Affiliation:
Centre d'Aqüicultura, Institut de Recerca i Tecnologia Agroalimentaries (IRTA), Aptat. Correus 200, 43540 Sant Carles de la Ràpita, Tarragona, Spain
Jose L. Zambonino-Infante
Affiliation:
UMR1067, Nutrition Aquaculture Génomique, IFREMER, 29280 Plouzané, France
Patrick Quazuguel
Affiliation:
UMR1067, Nutrition Aquaculture Génomique, IFREMER, 29280 Plouzané, France
Chantal L. Cahu
Affiliation:
UMR1067, Nutrition Aquaculture Génomique, IFREMER, 29280 Plouzané, France
*
*Corresponding author: Dr Laure Villeneuve, fax +33 298 224 366, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The effect of the nature and form of supply of dietary lipids on larval development was investigated in European sea bass larvae, by considering the expression of several genes involved in morphogenesis. Fish were fed from 7 to 37 d post-hatch with five isoproteic and isolipidic compound diets incorporating different levels of EPA and DHA provided by phospholipid or neutral lipid. Phospholipid fraction containing 1·1 % (PL1 diet) to 2·3 % (PL3 diet) of EPA and DHA sustained good larval growth and survival, with low vertebral and cephalic deformities. Similar levels of EPA and DHA provided by the neutral lipid fraction were teratogenic and lethal. Nevertheless, dietary phospholipids containing high levels of DHA and EPA (PL5 diet) induced cephalic (8·5 %) and vertebral column deformities (35·3 %) adversely affecting fish growth and survival; moreover, a down-regulation of retinoid X receptor α (RXRα), retinoic acid receptor α, retinoic acid receptor γ and bone morphogenetic protein-4 genes was also noted in PL5 dietary group at day 16. High levels of dietary PUFA in neutral lipid (NL3 diet) first up-regulated the expression of RXRα at day 16 and then down-regulated most of the studied genes at day 23, leading to skeletal abnormalities and death of the larvae. A moderate level of PUFA in neutral lipids up-regulated genes only at day 16, inducing a lesser negative effect on growth, survival and malformation rate than the NL3 group. These results showed that retinoid pathways can be influenced by dietary lipids leading to skeletal malformation during sea bass larvae development.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2005

References

Andrades, JA, Becerra, J & Fernandez-Llebrez, P (1994) Skeletal deformities of the gilthead sea bream ( Sparus aurata L.): study of the subcommisural organ (SCO) and Reissner's fiber (RF). Anat Anz 174, 381383.CrossRefGoogle Scholar
Balmer, JE & Blomhoff, R (2002) Gene expression regulation by retinoic acid. J Lipid Res 43, 17731808.CrossRefGoogle ScholarPubMed
Boglione, C, Gagliardi, F, Scardi, M & Cataudella, S (2001) Skeletal descriptors and quality assessment in larvae and post-larvae of wild-caught and hatchery-reared gilthead sea bream ( Sparus aurata L. 1758). Aquaculture 192, 122.CrossRefGoogle Scholar
Bonilla, S, Redonnet, A, Noël-Suberville, C, Pallet, V, Garcin, H & Higueret, P (2000) High-fat diets affect the expression of nuclear retinoic acid receptor in rat liver. Br J Nutr 83, 665671.CrossRefGoogle ScholarPubMed
Brinkmeyer, R & Holt, GJ (1998) Highly unsaturated fatty acids in diets for red drum (Scianops ocellatus) larvae. Aquaculture 161, 253268.CrossRefGoogle Scholar
Cahu, C, Zambonino-Infante, J & Takeuchi, T (2003a) Nutritional components affecting skeletal development in fish larvae. Aquaculture 227, 245258.CrossRefGoogle Scholar
Cahu, CL, Zambonino Infante, JL & Barbosa, V (2003b) Effect of dietary phospholipid level and phospholipid:neutral lipid value on the development of sea bass ( Dicentrarchus labrax ) larvae fed a compound diet. Br J Nutr 90, 2128.CrossRefGoogle ScholarPubMed
Dagnelie, P (1975) Les méthodes de l'inférence statistique. In Théorie et méthodes statistiques, vol. 2, pp. 1463 [Ducolot, J, editor]. Belgium: Les Presses Agronomiques de Gembloux.Google Scholar
Egea, PF, Rochel, N, Birck, C, Vachette, P, Timmins, PA & Moras, D (2001) Effects of ligand binding on the association and conformation in solution of retinoic acid receptors RXR and RAR. J Mol Biol 307, 557576.CrossRefGoogle ScholarPubMed
Fu, Z, Noguchi, T & Kato, H (2001) Vitamin A deficiency reduces insulin-like growth factor (IGF)-I gene expression and increases IGF-I receptor and insulin receptor gene expression in tissues of Japanese quail (Coturnix coturnix japonica). J Nutr 131, 11891194.CrossRefGoogle ScholarPubMed
Gabbitas, B & Canalis, E (1997) Retinoic acid regulates the expression of insulin-like growth factors I and II in osteoblasts. J Cell Physiol 172, 253264.3.0.CO;2-A>CrossRefGoogle Scholar
Gause, WC & Adamovicz, J (1994) The use of the PCR to quantitate gene expression. PCR Methods Appl 3, 123135.CrossRefGoogle ScholarPubMed
Gisbert, E, Villeneuve, L, Zambonino-Infante, JL, Quazuguel, P & Cahu, CL (2005) Dietary phospholipids are more efficient than neutral lipids for long chain polyunsaturated fatty acid supply in European sea bass Dicentrarchus labrax larval development. Lipids 40, 609618.CrossRefGoogle ScholarPubMed
Glozak, MA & Rogers, MB (1998) BMP4 and RA-induced apoptosis is mediated through the activation of retinoic acid receptors α and γ in P19 embryonal carcinoma cells. Exp Cell Res 242, 165173.CrossRefGoogle ScholarPubMed
Kliewer, SA, Sundseth, SS, Jones, SA, et al. (1997) Fatty acids and eicosanoids regulate gene expression through direct interactions with peroxisome proliferator-activated receptors α and γ. Proc Natl Acad Sci USA 94, 43184323.CrossRefGoogle ScholarPubMed
Krumlauf, R (1994) Hox genes in vertebrate development. Cell 78, 191201.CrossRefGoogle ScholarPubMed
Lemberger, T, Saladin, R, Vásquez, M, Assimacopoulos, F, Staels, B, Desvergne, B, Wahli, W & Auwerx, J (1996) Expression of the peroxisome proliferator-activated receptor α gene is stimulated by stress and follows a diurnal rhythm. J Biol Chem 271, 17641769.CrossRefGoogle Scholar
Mata de Urquiza, A, Liu, S, Sjöberg, M, Zetterström, RH, Griffiths, W, Sjöval, J & Perlmann, T (2000) Docosahexaenoic acid, a ligand for the retinoid X receptor in mouse brain. Science 290, 21402144.CrossRefGoogle Scholar
National Research Council (1985) Guide for the Care and Use of Laboratory Animals, Publication no. 85–23 (rev.). Bethesda, MD: National Institutes of Health.Google Scholar
National Research Council (1993) Nutrient Requirements of Fish. Washington, DC: National Academy Press.Google Scholar
Ogura, T & Evans, RM (1995) A retinoic acid-triggered cascade of HOXB1 gene activation. Proc Natl Acad Sci USA 92, 387391.CrossRefGoogle ScholarPubMed
Pfaffl, MW (2001) A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res 29, 20022007.CrossRefGoogle ScholarPubMed
Pfaffl, MW, Horgan, GW & Dempfle, L (2002) Relative expression software tool (REST ©) for group-wise comparison and statistical analysis of relative expression results in real-time PCR. Nucleic Acids Res 30, 936.CrossRefGoogle Scholar
Rodriguez, C, Perez, JA, Badia, P, Izquierdo, MS, Fernández-Palacios, H & Hernández, AL (1998) The n-3 highly unsaturated fatty acids requirements of gilthead sea bream ( Sparus aurata L.) larvae when using an appropriate ratio in the diet. Aquaculture 169, 923.CrossRefGoogle Scholar
Ross, SA, McCaffery, PJ, Drager, UC & De Luca, LM (2000) Retinoids in embryonal development. Physiol Rev 80, 10211054.CrossRefGoogle ScholarPubMed
Sargent, JR, McEvoy, LA & Bell, JG (1997) Requirements, presentation and sources of polyunsaturated fatty acids in marine larval fish. Aquaculture 155, 117127.CrossRefGoogle Scholar
Sargent, J, McEvoy, L, Estevez, A, Bell, G, Bell, M, Henderson, J & Tocher, D (1999) Lipid nutrition of marine fish during early development: current status and future directions. Aquaculture 179, 217229.CrossRefGoogle Scholar
Sargent, JR, Tocher, DR & Bell, JG (2002) The lipids. In Fish Nutrition, 3rd ed., pp. 182259 [Halver, JE and Hardy, RW, editors]. London: Academic Press.Google Scholar
Sasagawa, S, Takabatake, T, Takabatake, Y, Muramatsu, T & Takeshima, K (2002) Axes establishment during eye morphogenesis in Xenopus by coordinate and antagonistic actions of BMP4, shh, and RA. Genesis 33, 8696.CrossRefGoogle ScholarPubMed
Steineger, HH, Arnsten, BM, Spydevold, Ø & Sørensen, HN (1998) Gene transcription of the retinoid X receptor α (RXRα) is regulated by fatty acids and hormones in rat hepatic cells. J Lipid Res 39, 744754.CrossRefGoogle ScholarPubMed
Suzuki, T, Oohara, I & Kurokawa, T (1998) Hoxd-4 expression during pharyngeal arch development in flounder ( Paralichthys olivaceus ) embryos and effects of retinoic acid on expression. Zool Sci 15, 5767.CrossRefGoogle ScholarPubMed
Thompson, DL, Gerlach-Banck, LM, Barald, KF & Koenig, RJ (2003) Retinoic acid repression of bone morphogenetic protein 4 in inner ear development. Mol Cell Biol 23, 22772286.CrossRefGoogle ScholarPubMed
Villeneuve, L, Gisbert, E, Cahu, CL, Le Gall, MM & Zambonino-Infante, JL (2004) Expression and localization of some retinoid receptors during European sea bass ( Dicentrarchus labrax ) larvae development. Aquaculture 242, 537551.CrossRefGoogle Scholar
Villeneuve, L, Gisbert, E, Le Delliou, H, Cahu, CL & Zambonino-Infante, JL (2005) Dietary levels of all- trans retinol affect retinoid nuclear receptor expression and skeletal development in European sea bass larvae. Br J Nutr 93, 791801.CrossRefGoogle ScholarPubMed
Zambonino-Infante, JL, Cahu, CL & Péres, A (1997) Partial substitution of di- and tripeptides for native protein in sea bass diet improves Dicentrarchus labrax larval development. J Nutr 127, 604614.CrossRefGoogle ScholarPubMed