Iron Status of the Late Term Broiler (Gallus gallus) Embryo and Hatchling
DOI:
https://doi.org/10.3923/ijps.2011.42.48Keywords:
Broiler, brush border membrane, DMT1, embryo, ferritin, ironAbstract
Our objective was to investigate and elucidate the iron status of the late term broiler (Gallus gallus) embryo and young chick. This would be vital for better understanding of the transition period that the hatchling experience immediately after hatch. For that, blood, liver and small intestinal samples from broiler embryos were taken on embryonic days 12 (12E), 14E, 17E, 19E, day of hatch and 3 days post hatch. Expression of transporters and enzyme involved in Fe uptake and transfer, ie. Divalent metal transporter-1 (DMT1; iron uptake transporter), ferroportin (iron transport across the enterocyte) and duodenal cytochrome-B reductase (DcytB; reduces iron at brush border membrane) were determined. In addition, liver tissue samples were analyzed for iron and ferritin (cellular iron storage protein) contents. Samples were also collected from the intestinal contents, yolk sac, amniotic fluid and intestinal content for iron concentration analysis. The intestinal mRNA abundance of DMT1 and DcytB were shown to increase as from day 12E until day 17E, whereas ferroportin expression was unchanged. As from 19E a graduate decrease in relative expression occurred. Liver iron and ferritin concentrations were shown to decrease as from day 12E and as day of hatch approaches. In addition, yolk iron concentrations decreased while iron concentrations in amniotic fluid have increased (days 12E through 17E). This was followed by iron concentrations increase in the intestinal content (day 17E trough day of hatch). In this study, we first document the late term broiler embryo iron related enzyme and transporters gene expression as well as the changes in liver ferritin and liver iron contents.
References
llen, L.H. and J.M. Peerson, 2009. Impact of multiple micronutrient versus iron-folic acid supplements on maternal anemia and micronutrient status in pregnancy. Food Nutr. Bull., 30: S527-S532.
Aoyagi, S. and D.H. Baker, 1995. Iron requirement of chicks fed a semipurified diet based on casein and soy protein concentrate. Poult. Sci., 74: 412-415.
Bauminger, E.R., S.G. Cohen, S. Ofer and U. Bachrach, 1982. Study of storage iron in cultured chick embryo fibroblasts and rat glioma cells, using Mossbauer spectroscopy. Biochem. Biophys. Acta, 720: 133-140.
Dewar, W.A., P.W. Teague and J.N. Downie, 1974. The transfer of minerals from the egg to the chick embryo from the 5th to 18th days of incubation. Br. Poult. Sci., 15: 119-129.
Geyra, A., Z. Uni and D. Sklan, 2001. The effect of fasting at different ages on growth and tissue dynamics in the small intestine of the young chick. Br. J. Nutr., 86: 53-61.
Klempa, K.L., W.T. Willis, R. Chengson, P.R. Daalman and G.A. Brooks, 1989. Iron deficiency decreases gluconeogenesis in isolated rat hepatocytes. J. Applied Physiol., 67: 1868-1872.
Li, M. and C. Zhao, 2009. Study on Tibetan chicken embryonic adaptability to chronic hypoxia by revealing differential gene expression in heart tissue. Sci. China. C. Life. Sci., 52: 284-295.
Liu, C., L.F. Zhang, M.L. Song, H.G. Bao, C.J. Zhao and N. Li, 2009. Highly efficient dissociation of oxygen from hemoglobin in Tibetan chicken embryos compared with lowland chicken embryos incubated in hypoxia. Poult. Sci., 88: 2689-2694.
Ludwiczek, S., I. Theurl, E. Artner-Dworzak, M. Chorney and G. Weiss, 2004. Duodenal HFE expression and hepcidin levels determine body iron homeostasis: Modulation by genetic diversity and dietary iron availability. J. Mol. Med., 82: 373-382.
Marchaim, U. and R.G. Kulka, 1967. The non-parallel increase of amylase, chymotrypsinogen and procarboxypeptidase in the developing chick pancreas. Bioch. Biophys. Acta, 146: 553-559.
Mete, A., Y.R.A. van Zeeland, A.B. Vaandrager, J.E. van Dijk, J.J. Marx and G.M. Dorrestein, 2005. Partial purification and characterization of ferritin from the liver and intestinal mucosa of chickens, turtledoves and mynahs. Avian Pathol., 34: 430-434.
Nitsan, Z., I. Turro-Vincent, G. Liu, E.A. Dunnington and P.B. Siegel, 1995. Intubation of weight-selected chicks with soybean oil or residual yolk: Effect on early growth and development. Poult. Sci., 74: 925-936.
Noy, Y. and D. Sklan, 1998. Yolk utilisation in the newly hatched poult. Br. Poult. Sci., 39: 446-451.
Noy, Y. and D. Sklan, 2002. Nutrient use in chicks during the first week posthatch. Poult. Sci., 81: 391-399.
NRC, 1994. Nutrition Requirements of Poultry. 9th Rev. Edn., National Acadmic Press, Washington, DC.
Passaniti, A. and T.F. Roth, 1989. Purification of chicken liver ferritin by two novel methods and structural comparison with horse spleen ferritin. Biochem. J., 258: 413-419.
Pietrangelo, A., G. Casalgrandi, D. Quaglino, R. Gualdi and D. Conte et al., 1995. Duodenal ferritin synthesis in genetic hemochromatosis. Gastroenterology, 108: 208-217.
Richards, M.P. and N.C. Steele, 1987. Trace element metabolism in the developing avian embryo: A review. J. Exp. Zool. Suppl., 1: 39-51.
Richards, M.P., 1991. Mineral metabolism in the developing turkey embryo-I. The effects of developmental age and shell-less culture on trace element contents of selected tissues. Comp. Biochem. Physiol., 100: 1009-1016.
Richards, M.P., 1997. Trace mineral metabolism in the avian embryo. Poult. Sci., 76: 152-164.
Ramsay, W.N.M., 1951. Iron metabolism and haemoglobin formation in the embryonated hen egg. 2. Some observations on the embryonic blood supply. J. Bioch., 49: 494-499.
Romanoff, A., 1967. Biochemistry of the Avian Embryo. Macmillan, New York.
Savage, J.E., 1968. Trace minerals and avian reproduction. Fed. Proc., 27: 927-931.
Scott, G.R., V. Cadena, G.J. Tattersall and W.K. Milsom, 2008. Body temperature depression and peripheral heat loss accompany the metabolic and ventilatory responses to hypoxia in low and high altitude birds. J. Exp. Biol., 211: 1326-1335.
Sinclair, P.R., W.J. Bement, N. Gorman, H.H. Liem, A.W. Wolkoff and U. Mullen-Eberhard, 1988. Effect of serum proteins on haem uptake and metabolism in primary cultures of liver cells. Biochem. J., 256: 159-165.
Tako, E., P.R. Ferket and Z. Uni, 2004. Effects of in ovo feeding of carbohydrates and β-hydroxy-β-methylbutyrate on the development of chicken intestine. Poult. Sci., 83: 2023-2028.
Tako, E., P.R. Ferket and Z. Uni, 2005. Changes in chicken intestinal zinc exporter mRNA expression and small intestinal functionality following intra-amniotic zinc-methionine administration. J. Nutr. Biochem., 16: 339-346.
Tako, E., M.A. Rutzke and R.P. Glahn, 2010. Using the domestic chicken (Gallus gallus) as an in vivo model for iron bioavailability1. Poult. Sci., 89: 514-521.
Tako, E. and R.P. Glahn, 2011. White beans provide more bioavailable iron than red beans: Studies in poultry (Gallus gallus) and an in vitro digestion/Caco-2 model. Int. J. Vit. Nutr. Res., (In Press).
Theil, E.C. and G.M. Tosky, 1979. Red cell ferritin and iron storage during chick embryonic development. Dev. Biol., 69: 666-672.
Theil, E.C., 1980. Embryonic erythropoiesis and iron metabolism. Br. J. Haematol., 45: 357-360.
Uni, Z., A. Smirnov and D. Sklan, 2003. Pre- and posthatch development of goblet cells in the broiler small intestine: Effect of delayed access to feed. Poult. Sci., 82: 320-327.
Uni, Z., E. Tako, O. Gal-Garber and D. Sklan, 2003. Morphological, molecular and functional changes in the chicken small intestine of the late-term embryo. Poult. Sci., 82: 1747-1754.
Uni, Z., P.R. Ferket, E. Tako and O. Kedar, 2005. In ovo feeding improves energy status of late-term chicken embryos. Poult. Sci., 84: 764-770.
Wei, Z.H., H. Zhang, C.L. Jia, Y. Ling, X. Gou, X.M. Deng and C.X. Wu, 2007. Blood gas, hemoglobin and growth of tibetan chicken embryos incubated at high altitude. Poult. Sci., 86: 904-908.
White, H., 1991. Maternal Diet, Maternal Proteins and Egg Quality. In: Egg Incubation: Its Effects on Embryonic Development in Birds and Reptiles. Deeming, D.C. and M.W.J. Ferguson (Eds.). Cambridge University Press, Cambridge, UK., pp: 1-5.
Whitnall, M. and D.R. Richardson, 2006. Iron: A new target for pharmacological intervention in neurodegenerative diseases. Seminars Pediatric Neurol., 13: 186-197.
Lozoff, B., N. Kacirot and T. Walter, 2006. Iron deficiency in infancy: Applying a physiologic framework for prediction. Am. J. Clin. Nutr., 84: 1412-1421.
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