Hostname: page-component-76fb5796d-22dnz Total loading time: 0 Render date: 2024-04-25T20:40:47.632Z Has data issue: false hasContentIssue false

Pre- and postprandial changes in plasma hormone and metabolite levels and hepatic deiodinase activities in meal-fed broiler chickens

Published online by Cambridge University Press:  09 March 2007

Johan Buyse*
Affiliation:
Laboratory for Physiology and Immunology of Domestic Animals, Department of Animal Production, Katholieke Universiteit Leuven, Kasteelpark Arenberg 30, 3001 Leuven, Belgium
Kristel Janssens
Affiliation:
Laboratory of Comparative Endocrinology, Katholieke Universiteit Leuven, Naamsestraat 61, 3000 Leuven, Belgium
Serge Van der Geyten
Affiliation:
Laboratory of Comparative Endocrinology, Katholieke Universiteit Leuven, Naamsestraat 61, 3000 Leuven, Belgium
Pieter Van As
Affiliation:
Laboratory for Physiology and Immunology of Domestic Animals, Department of Animal Production, Katholieke Universiteit Leuven, Kasteelpark Arenberg 30, 3001 Leuven, Belgium
Eddy Decuypere
Affiliation:
Laboratory for Physiology and Immunology of Domestic Animals, Department of Animal Production, Katholieke Universiteit Leuven, Kasteelpark Arenberg 30, 3001 Leuven, Belgium
Veerle M. Darras
Affiliation:
Laboratory of Comparative Endocrinology, Katholieke Universiteit Leuven, Naamsestraat 61, 3000 Leuven, Belgium
*
*Corresponding author: Dr J. Buyse, fax +32 16 321994, email johan.buyse@agr.kuleuven.ac.be
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 present study aimed to study the effects of food deprivation and subsequent postprandial changes in plasma somatotrophic and thyrotrophic hormone levels and focused on the inter-relationships between these hormonal axes and representative metabolites of the intermediary metabolism of meal-fed broiler chickens. Male broiler chickens (2 weeks old) were fed a meal of 40–45 g/bird per d for two consecutive weeks (food-restricted (FR) treatment). The daily allowance was consumed in about 30 min. At 4 weeks of age, FR chickens were killed at several time intervals (ten per sampling time) in relation to the daily food allowance: before feeding (about 23·5 h of food deprivation), and at 10, 20, 30 (end of feeding), 40, 50, 60, 90, 120 and 200 min after initiation of feeding. Birds fed ad libitum served as controls (ad-libitum (AL) treatment). Liver tissue was collected for deiodinase type I and type III activity measurements and blood samples for analysis of growth hormone (GH), insulin-like growth factor (IGF)-I, thyroxine (T4), 3,3′,5-triiodothyronine (T3), glucose, non-esterified fatty acids (NEFA), uric acid, triacylglycerol (TG) and lactate levels. Food deprivation caused a shift from lipogenesis to lipolysis and increased fatty acid turnover, a reduction in protein anabolism and reduced metabolic rate. Food intake was followed immediately by a pronounced increase in metabolic rate, initially mainly based on anaerobic mechanisms. Refeeding gradually reversed the fasting-induced alterations in plasma hormone and metabolite levels, but the time course of changes differed between metabolites, which clearly preceded those of the hormones investigated. The order of responsiveness after food provision were glucose>uric acid≥NEFA>lactate>TG for the plasma metabolites and GH>T3>T4>IGF–I for hormones. Based on these different postprandial time courses, several functional relationships are proposed. Glucose is believed to be the primary trigger for the normalisation of the effects of fasting on these plasma variables by restoring hepatic GH receptor capacity, as well as decreasing deiodinase type III activity.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2002

References

Aman Yaman, M, Kita, K & Okumura, K (2000) Different responses of protein synthesis to refeeding in various muscles of fasted chickens. British Poultry Science 41, 224228.CrossRefGoogle Scholar
Anthony, NB, Vasilatos-Younken, R, Bacon, WL & Lilburn, MS (1990) Secretory pattern of growth hormone, insulin and related metabolites in growing male turkeys – effects of overnight fasting and refeeding. Poultry Science 69, 801811.CrossRefGoogle ScholarPubMed
Bacon, WL (1986) Age and short-term feed restriction effects on plasma triglyceride and free fatty acid concentrations in male turkeys. Poultry Science 65, 19451948.CrossRefGoogle ScholarPubMed
Berghman, L, Van Beeumen, E, Decuypere, E, Kühn, ER & Vandesande, F (1988) One step purification of chicken growth hormone from a crude pituitary extract by use of a monoclonal immunoadsorbent. Journal of Endocrinology 108, 381387.CrossRefGoogle Scholar
Bensadoun, A & Rothfield, A (1972) The form of absorption of lipids in the chicken, Gallus domesticus. Proceedings of the Society for Experimental Biology and Medicine 41, 814817.CrossRefGoogle Scholar
Brameld, JM, Gilmore, RS & Buttery, PJ (1999) Glucose and amino acids interact with hormones to control expression of insulin-like growth hormone-I and growth hormone receptor mRNA in cultured pig hepatocytes. Journal of Nutrition 129, 12981306.CrossRefGoogle Scholar
Buyse, J, Darras, VM, Vleurick, L, Kühn, ER & Decuypere, E (2001a) Nutritional regulation of the somatotrophic axis and intermediary metabolism in the chicken. In Avian Endocrinology, pp. 303313 [Dawson, A and Chaturvedi, CM, editors]. New Dehli: Narosa Publishing House.Google Scholar
Buyse, J & Decuypere, E (1999) The role of the somatotrophic axis in the metabolism of the chicken. Domestic Animal Endocrinology 17, 245255.CrossRefGoogle Scholar
Buyse, J, Decuypere, E, Darras, VM, Vleurick, LM, Kühn, ER & Veldhuis, JD (2000) Food deprivation and feeding is associated with rapid and interdependent changes in the somatotropic and thyrothrophic axes. British Poultry Science 41, 107116.CrossRefGoogle Scholar
Buyse, J, Decuypere, E & Kühn, ER (1995) Effect of progressive fasting on physiological criteria of adult Warren SSL hens. Hormone and Metabolic Research 27, 482484.CrossRefGoogle ScholarPubMed
Buyse, J, Decuypere, E, Leenstra, FR & Scanes, CG (1992) Abdominal adipose tissue from broiler chickens selected for body weight or for food efficiency differ in their.in vitro lipolytic sensitivity to glucagon and growth hormone but not to dibutyryl-cAMP. British Poultry Science 33, 10691075.CrossRefGoogle ScholarPubMed
Buyse, J, Janssens, GPJ & Decuypere, E (2001b) The effects of l-carnitine supplementation on the performance, organ weights and circulating hormone and metabolite concentrations of broiler chickens reared under a normal or low temperature schedule. British Poultry Science 43, 230241.CrossRefGoogle Scholar
Chineme, CN, Buyse, J, Buys, N, Hassanzadeh Ladmakhi, M, Albers, G & Decuypere, E (1995) Interaction of genotype, egg shell conductance and dietary T3 supplementation in the development of heart failure syndrome and ascites in broiler chickens. Archiv für Geflügelkunde 59, 129134.Google Scholar
Costa, MJ (1981) Fundamental principles of broiler breeders nutrition and the design of feeding programs. World's Poultry Science Journal 37, 177192.CrossRefGoogle Scholar
Darras, VM, Visser, TJ, Berghman, LR & Kühn, ER (1992) Ontogeny of type I and type III deiodinase activities in embryonic and posthatch chickens: relationship with changes in plasma triiodothyronine and growth hormone levels. Comparative Biochemistry and Physiology 103A, 131136.CrossRefGoogle Scholar
Decuypere, E & Kühn, ER (1984) Effect of fasting and feeding time on circadian rhythms of serum thyroid hormone concentrations, glucose, liver monodeiodinase activity and rectal temperature in growing chickens. Domestic Animal Endocrinology 1, 251262.CrossRefGoogle Scholar
Gavin, LA & Moeller, M (1983) The mechanisms of recovery of hepatic T4-5'-deiodinase during glucose-refeeding: role of glucagon and insulin. Metabolism 32, 543551.CrossRefGoogle Scholar
Goodridge, AG, Crish, JF, Hillgartner, FB & Wilson, SB (1989) Nutritional and hormonal regulation of the gene for avian malic enzyme. Journal of Nutrition 119, 299308.CrossRefGoogle ScholarPubMed
Harvey, S, Fraser, RA & Lea, RW (1991) Growth hormone secretion in poultry. Critical Reviews in Poultry Biology 3, 239282.Google Scholar
Harvey, S & Klandorf, H (1983) Reduced adrenocortical function and increased thyroid function in fasted and refed chickens. Journal of Endocrinology 98, 129135.CrossRefGoogle ScholarPubMed
Hocking, PM, Maxwell, MH & Mitchell, MA (1996) Relationships between the degree of food restriction and welfare indices in broiler breeder females. British Poultry Science 37, 263278.CrossRefGoogle ScholarPubMed
Huybrechts, LM, King, DB, Lauterio, TJ, Marsh, J & Scanes, CG (1985) Plasma concentrations of somatomedin-C in hypophysectomized, dwarf and intact growing domestic fowl as determined by heterologous radioimmunoassay. Journal of Endocrinology 104, 233239.CrossRefGoogle ScholarPubMed
Hull, KL & Harvey, S (1998) Autoregulation of central and peripheral growth hormone receptor mRNA in domestic fowl. Journal of Endocinology 156, 323329.CrossRefGoogle ScholarPubMed
Kita, K, Hangsanet, K & Okumura, J (1998a) Influence of refeeding of protein, carbohydrate and fat on hepatic insulin-like growth factor-I mRNA level in fasted chicks. Asian–Australian Journal of Animal Sciences 11, 245248.CrossRefGoogle Scholar
Kita, K, Hangsanet, K, Shibata, T, Conlon, MA, Sasaki, T, Saito, N & Okumura, J (1998b) Refeeding increases hepatic insulin-like growth factor-I (IGF-I) gene expression and plasma IGF-I concentration in fasted chicks. British Poultry Science 39, 679682.CrossRefGoogle ScholarPubMed
Klandorf, H & Harvey, S (1985) Food intake regulation of circulating thyroid hormones in the domestic fowl. General and Comparative Endocrinology 60, 162170.CrossRefGoogle ScholarPubMed
Klandorf, H, Sharp, PJ & MacLeod, MG (1981) Relationship between heat production and concentrations of plasma thyroid hormones in the domestic hen. General and Comparative Endocrinology 45, 513520.CrossRefGoogle ScholarPubMed
Langslow, DR & Lewis, RJ (1974) Alterations with age in composition and lipolytic activity of adipose tissue from male and female chickens. British Poultry Science 15, 267273.CrossRefGoogle ScholarPubMed
Leveille, GA, Romsos, DR, Yeh, YY & O'Hea, EK (1975) Lipid biosynthesis in the chick. A consideration of site of synthesis, influence of diet and possible regulatory mechanisms. Poultry Science 54, 10751093.CrossRefGoogle Scholar
Lien, TF, Chou, RCR, Chen, SY, Jeng, YI & Jan, DF (1999) Lipid metabolism of Tsaiya ducks: plasma and liver related traits under ad libitum and fasting. Journal of the Science of Food and Agriculture 79, 14131416.3.0.CO;2-K>CrossRefGoogle Scholar
Lien, TF, Wu, CP, Chen, KL & Yang, KH (2000) Effects of different fatty acids in the lipogenesis capacity and lipolysis of broilers in vitro. Asian–Australian Journal of Animal Sciences 23, 12851289.CrossRefGoogle Scholar
Niimi, S, Hayakawa, T, Tanaka, A & Ichihara, A (1991) Glucose regulation of growth hormone receptors in primary cultured rat hepatocytes. Endocrinology 129, 27342739.CrossRefGoogle ScholarPubMed
Okumura, L & Kita, K (1999) Recent advances in the relationship between endocrine status and nutrition in chickens. Asian–Australian Journal of Animal Sciences 12, 11351141.CrossRefGoogle Scholar
Simon, J (1991) Chicken as a useful species for the comprehension of insulin action. Critical Reviews in Poultry Biology 2, 121148.Google Scholar
Stryer, L (1981) Biochemistry, 2nd ed. San Francisco, CA: W. H. Freeman and Company.Google Scholar
Tsukada, A, Ohkubo, T, Sakaguchi, K, Tanaka, M, Nakashimi, K, Hayashida, Y, Wakita, M & Hoshino, S (1998) Thyroid hormones are involved in insulin-like growth factor-I (IGF-I) production by stimulating hepatic growth hormone receptor (GHR) gene expression in the chicken. Growth Hormone and Insulin-Like Growth Factor Research 8, 235242.CrossRefGoogle ScholarPubMed
Van As, P, Janssens, W, Onagbesan, OM, Buys, N, Sanders, J, Van der Geyten, S, Darras, VM & Decuypere, E (2001) Quantification of growth hormone receptor extra- and intracellular domain gene expression in chicken liver by quantitative competitive RT-PCR. General and Comparative Endocrinology 122, 213224.CrossRefGoogle ScholarPubMed
Van der Geyten, S, Van Rompaey, E, Sanders, JP, Visser, TJ, Kühn, ER & Darras, VM (1999) Regulation of thyroid hormone metabolism during fasting and refeeding in chicken. General and Comparative Endocrinology 116, 272280.CrossRefGoogle ScholarPubMed
Vanderpooten, A, Dewil, E, Decuypere, E & Kühn, ER (1989) The effect of fasting on growth hormone receptor in liver membranes of adult chickens. Medical Science Research 17, 10311032.Google Scholar
Vasilatos-Younken, R, Cravener, TL, Cogburn, LA, Mast, MG & Wellenreiter, RK (1988) Effect of pattern of administration on the response to exogenous, pituitary-derived chicken growth hormone by broiler strain pullets. General and Comparative Endocrinology 71, 268283.CrossRefGoogle ScholarPubMed
Vasilatos-Younken, R, Zhou, Y, Wang, X, McMurtry, JP, Rosebrough, RW, Decuypere, E, Buys, N, Darras, VM, Van der Geyten, S & Tomas, F (2000) Altered chicken thyroid hormone metabolism with chronic GH enhancement in vivo: consequences for skeletal muscle growth. Journal of Endocrinology 166, 609620.CrossRefGoogle ScholarPubMed