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Effect of Supplementing the Diet of Olive Flounder Paralichthys olivaceus with Sea Mustard Undaria pinnatifida Glycoprotein on Growth and the Immune System

사료 내 미역(Undaria pinnatifida) 당단백질의 첨가가 넙치(Paralichthys olivaceus) 치어의 성장 및 면역 증강에 미치는 영향

  • An, Cheul-Min (Aquafeed Research Center, National Fisheries Research & Development Institute) ;
  • Kim, Kang-Woong (Aquafeed Research Center, National Fisheries Research & Development Institute) ;
  • Kim, Kyoung-Duck (Aquafeed Research Center, National Fisheries Research & Development Institute) ;
  • Kim, Young-Min (Department of Food Science and Nutrition, Pukyong National University) ;
  • Kim, In-Hye (Department of Food Science and Nutrition, Pukyong National University) ;
  • Park, Su-Jin (Department of Food Science and Nutrition, Pukyong National University) ;
  • Choi, Youn Hee (Institute of Fisheries Sciences, Pukyong National University) ;
  • Nam, Taek Jeong (Department of Food Science and Nutrition, Pukyong National University)
  • 안철민 (국립수산과학원 사료연구센터) ;
  • 김강웅 (국립수산과학원 사료연구센터) ;
  • 김경덕 (국립수산과학원 사료연구센터) ;
  • 김영민 (부경대학교 식품영양학과) ;
  • 김인혜 (부경대학교 식품영양학과) ;
  • 박수진 (부경대학교 식품영양학과) ;
  • 최윤희 (부경대학교 수산과학연구소) ;
  • 남택정 (부경대학교 식품영양학과)
  • Received : 2012.07.26
  • Accepted : 2012.10.18
  • Published : 2012.10.31

Abstract

This study evaluated the effects of adding sea mustard Undaria pinnatifida glycoprotein to the diet of juvenile olive flounder Paralichthys olivaceus on its growth, and levels of insulin-like growth factor I (IGF-I), IGF binding proteins (IGFBPs), and interleukins. Three experimental diets (U0, U0.5, and U1.0) were formulated that contained different amounts of an extract of U. pinnatifida (0, 0.5, and 1.0%, respectively). Experimental groups were established in triplicate (30 fish/group) and fed for 12 weeks. The experimental group fed 1.0% added U. pinnatifida glycoprotein had the greatest rate of weight gain, which differed significantly from the other experimental groups. SDS-PAGE of the plasma IGF-I and muscle protein showed that the experimental groups taking U. pinnatifida glycoprotein had significantly more IGF-I and a ca. 200 kDa protein, as compared to the control group. In addition, the amount of IGFBP-3 at ca. 43 kDa increased in the group given the U. pinnatifida extract, as compared to the control group. The interluekin-2, -4, -6, and -12 levels paralleled the level of growth factor in the groups given the U. pinnatifida extract. In conclusion, supplementing the diet of olive flounder with U. pinnatifida glycroprotein improved its growth and immunity.

Keywords

References

  1. Baxter RC. 1993. Circulating binding proteins for the insulinlike growth factors. Trends Endocrinol Metab 4, 91-96. https://doi.org/10.1016/1043-2760(93)90085-S
  2. Cha BK, Chang MW, Jung YK, Kim KH. 2006. Effects of Eucalyptus and Geranium on Production of IL-2 and IL-4 in Mouse Splenocytes. J Life Sci 16, 162-167. https://doi.org/10.5352/JLS.2006.16.1.162
  3. Duan C and Xu Q. 2005. Roles of insulin-like growth factor (IGF) binding proteins in regulating IGF actions. Gen Comp Endocrinol 142, 44-52. https://doi.org/10.1016/j.ygcen.2004.12.022
  4. Gutierrez J, Asgard T, Fabbri E and Plisetskaya EM. 1991. Insulin-receptor binding in skeletal-muscle of trout. Fish Physiol Biochem 9, 351-360. https://doi.org/10.1007/BF02265155
  5. Hwang HJ, Kwon MJ, Kim IH, Nam TJ. 2008. Chemoprotective effects of a protein from the red algae Porphyra yezoensis on acetaminophen-induced liver injury in rats. Phytother Res 22, 1149-53. https://doi.org/10.1002/ptr.2368
  6. Hirayasu H, Yoshikawa Y, Tsuzuki S and Fushiki T. 2005. Sulfated polysaccharides derived from dietary seaweeds increase the esterase activity of a lymphocyte tryptase, granzyme A. J Nutr Sci Vitaminol 51, 475-477. https://doi.org/10.3177/jnsv.51.475
  7. Kim KD, Seo JY, Hong SH, Kim JH, Byun HG, Kim KW, Son MH and Lee SM. 2011. Effects of dietary inclusion of various additives on growth performance, hematological parameters, fatty acid composition, gene expression and histopathological changes in juvenile olive flounder Paralichthys olivaceus. Kor J Fish Aquat Sci 44, 141-148. https://doi.org/10.5657/kfas.2011.44.2.141
  8. Kim SS, Jang JW, Song JW, Lim SJ, Jeong JB, Lee SM, Kim KW, Son MH and Lee KJ. 2009. Effects of dietary supplementation of alga mixtures (Hizikia fusiformis and Ecklonia cava) on innate immunity and disease resistance against Edwardsiella tarda in olive flounder (Paralichthys olivaceus). Kor J Fish Aquat Sci 42, 614-620. https://doi.org/10.5657/kfas.2009.42.6.614
  9. Kim SS and Lee KJ. 2008. Effects of dietary kelp (Ecklonia cava) on growth and innate immunity in juvenile olive flounder Paralichthys olivaceus (Temminck et Schlegel). Aquacult Res 39, 1687-1690.
  10. Maeda H, Hosokawa M, Sashima T, Funayama K and Miyashita K. 2005. Fucoxanthin from edible seaweed, Undaria pinnatifida, shows antiobesity effect through UCP1 expression in white adipose tissues. Biochem Biophys Res Commun 332, 392-397. https://doi.org/10.1016/j.bbrc.2005.05.002
  11. Moriyama S, Ayson FG and Kawauchi H. 2000. Growth regulation by insulin-like growth factor-I in fish. Biotechnol Biochem 64, 1553-1562. https://doi.org/10.1271/bbb.64.1553
  12. Nam TJ, Lee SM and Pyeun JH. 1998. Effects of insulin-like growth factor-I (IGF-I) on body weight and the concentration of serum IGF binding proteins in Korean rockfish (Sebastes schlegeli). J Korean Fish Soc 31, 774-778.
  13. Park SH. 2006. The Regulation of Insulin-Like Growth (IGF) Factors and IGF Binding Proteins by High Glucose in Mesangial Cell. J Exp Biomed Sci 10, 203-210.
  14. Pham MA, Lee KJ, Lee BJ, Lim SJ, Kim SS, Lee YD, Heo MS and Lee KW. 2006. Effects of dietary Hizikia fusiformis on growth and immune responses in juvenile olive flounder (Paralichthys olivaceus). Ian-Aust J Anim Sci 19, 1769- 1775. https://doi.org/10.5713/ajas.2006.1769
  15. Peter RE and Marchant TA. 1995. The endocrinology of growth in carp and related species. Aquaculture 129, 299-321. https://doi.org/10.1016/0044-8486(94)00302-5
  16. Peterson BC and Small BC. 2005. Effects of exogenous cortisol on the GH/IGF-I/IGFBP network in channel catfish. Domest Anim Endocrinol 28, 391-404. https://doi.org/10.1016/j.domaniend.2005.01.003
  17. Peterson BC and Waldbieser GC. 2009. Effects of fasting on IGF-I, IGF-II, and IGF-binding protein mRNA concentrations in channel catfish (Ictalurus punctatus). Domest Anim Endocrinol 37, 74-83. https://doi.org/10.1016/j.domaniend.2009.03.004
  18. Planas JV, Mendez E, Banos N, Capilla E, Navarro I and Gutierrez J. 2000. Insulin and IGF-I receptors in trout adipose tissue are physiologically regulated by circulating hormone levels. J Exp Biol 203, 1153-1159.
  19. Refstie S, Storebakken T, Baeverfjord G and Roem AJ. 2001. Long-term protein and lipid growth of Atlantic salmon (Salmo salar) fed diets with partial replacement of fish meal by soy protein products at medium or high lipid level. Aquaculture 193, 91-106. https://doi.org/10.1016/S0044-8486(00)00473-7
  20. Ryu HS, Kim KO, Kim HS. 2009. Effects of plant water extract Codonopsis Lanceolatae on mouse immune cell activation ex vivo. Korean J Nutr 42, 207-212. https://doi.org/10.4163/kjn.2009.42.3.207
  21. Soler-Vila A, Coughlan S, Guiry MD and Kraan S. 2009. The red alga Porphyra dioica as a fish-feed ingredient for rainbow trout (Oncorhynchus mykiss): effects on growth, feed efficiency, and carcass composition. J Appl Phycol 21, 617-624. https://doi.org/10.1007/s10811-009-9423-z
  22. Song JW, Jang JW, Kim SS, Oh DH, Cha JH and Lee KJ. 2011. Effect of dietary supplementation with alga (Hizikia fusiformis and Ecklonia cava) on the non-specific immune responses of parrot fish Oplegnathus fasciatus. Kor J Fish Aquat Sci 44, 332-338. https://doi.org/10.5657/KFAS.2011.0332
  23. Vera Cruz EM, Brown CL, Luckenbach JA, Picha ME, Bolivar RB and Borski RJ. 2006. Insulin-like growth factor-I cDNA cloning, gene expression and potential use as a growth rate indicator in Nile tilapia, Oreochromis niloticus. Aquaculture 251, 585-595. https://doi.org/10.1016/j.aquaculture.2005.06.039
  24. Yuan YV and Walsh NA. 2006. Antioxidant and antiproliferative activities of extracts from a variety of edible seaweeds. Food Chem Toxicol 44, 1144-1150. https://doi.org/10.1016/j.fct.2006.02.002

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