Hostname: page-component-78c5997874-dh8gc Total loading time: 0 Render date: 2024-11-10T16:58:16.087Z Has data issue: false hasContentIssue false

Crude protein and supplemental dietary tryptophan effects on growth and tissue neurotransmitterlevels in the broiler chicken*

Published online by Cambridge University Press:  09 March 2007

R.W Rosebrough
Affiliation:
Growth Biology Laboratory, Livestock and Poultry Sciences Institute, United States Department of Agriculture-Agricultural Research Service, Beltsville Agricultural Research Center, Beltsville, MD 20705, USA
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.

Indian River male broiler chickens growing from 7 to 28 d of age were fed on diets containing 120,210 and 300 g crude protein/kg diet and 0, 1–67 or 16·7 g added tryptophan (TRP)/kg diet. The hypothesis tested was that crude protein levels and TRP would affect both growth and neurotransmitter metabolism. Heart, brain and pancreatic neurotransmitter (noradrenaline (NA), dopamine(DA), serotonin (5-HT) and 5-hydroxy-indole-3-acetic acid (5-HIAA) concentrations were determined by HPLC separation and electrochemical detection. Malate dehydrogenase (2-oxoglntarate decarboxylating) (NADP+) (MDH(NADP+); EC 1.1.1.40), isocitrate dehydrogenase (NADP+) (ICD(NADP+); EC 1.1.1.42) and aspartate aminotransferase (AAT; EC 2.6.1.1) activities were also measured. Supplemental TRP decreased growth and feed intake. Increasing dietary crude protein decreased MDH(NADP+), but increased (ICD(NADP+) and AAT activities. Additional dietary TRP decreased MDH(NADP+) activity, but had no effect on other enzyme activities. Cardiac NA concentrations were directly related to dietary crude protein levels while pancreatic levels were inversely related. An increase in dietary crude protein decreased both brain NA and DA. Supplemental dietary TRP increased both 5- HIAA and 5-HT. Changes in feed intake caused by different levels of botb dietary crude protein and TRP are accompanied by altered levels of neurotransmitters. The present study indicates that much arger amounts of TRP are required to make simultaneous changes in feed intake and neurotransmitters.

Type
Animal Nutrition
Copyright
Copyright © The Nutrition Society 1996

References

REFERENCES

Anton, A. H. & Sayre, D. F. (1962). A study of the factors affecting the aluminum oxide trihydroxyindole procedure for the analysis of catecholamines. Journal of Pharmacology and Experimental Therapeutics 138, 360375.Google ScholarPubMed
Cleland, W. W., Thompson, V. M. & Barden, R. E. (1969). Isocitrate dehydrogenase (TPN specific) from pig heart. In Methods in Enzymology, vol. 13, pp. 3033 [Lowenstein, J. M., editor]. New York: Academic Press.Google Scholar
Colmenares, J. L., Wurtman, R. J. & Fernstrom, J. D. (1975). Effects of ingestion of a carbohydrate-fat meal on the levels and synthesis of 5-hydroxyindoles in various regions of the ratcentral nervous system. Journal of Neurochemistry 25, 825829.CrossRefGoogle ScholarPubMed
Denbow, D. M. (1983). Food intake and temperature response to injections of catcholamines into the lateral ventricle of the turkey brain. Poultry Science 62, 10881092.CrossRefGoogle Scholar
Denbow, D. M., Hobbs, F. C., Hulet, R. M., Graham, P. P. & Potter, L. M. (1993). Supplemental dietary L-tryptophan effects on growth, meat quality, and brain catecholamine and indolamineconcentrations in turkeys. British Poultry Science 34, 715–124.CrossRefGoogle ScholarPubMed
Denbow, D. M. & Sheppard, B. J. (1993). Food and water intake responses of the domestic fowl to norepinephrine infusion at circumscribed neural sites. Brain Research Bulletin 31, 121128CrossRefGoogle ScholarPubMed
Eriksson, B.-M. & Persson, B.-A. (1982). Determination of catecholamines in rat heart tissue and plasma samples by liquid chromatography and electrochemical detection. Journal of Chromatography 228, 143154.CrossRefGoogle ScholarPubMed
Fernstrom, J. D. (1979). Diet-induced changes in plasma amino acid pattern: effects on the brain uptake of large neutral amino acids, and on brain serotonin synthesis. Journal of Neural Transmission 15, 217219.Google Scholar
Fernstrom, J. D. (1983). Role of precursor availability in control of monoamine biosynthesis inbrain. Physiological Reviews 93, 484546.CrossRefGoogle Scholar
Goldman, C. K., Marino, L. & Leibowitz, S. F. (1985). Postsynaptic α2-noradrenergic receptors mediate feeding induced by paraventricular nucleus injection of norepinephrine and clonidine. European Journal of Pharmacology 115, 1119.CrossRefGoogle Scholar
Hsu, R. Y. & Lardy, H. A. (1969). Malic enzyme. In Methods in Enzymology, vol. 13, pp. 230235 [Lowenstein, J. M., editor]. New York: Abdemic Press.Google Scholar
Kaufman, L. N., Young, J. B. & Landsberg, L. (1984). Protein stimulates sympathetic nervous(CNS) activity less than carbohydrate: evidence for nutrient-specific CNS responses. Clinical Research 32, 478490.Google Scholar
Kaufman, L. N., Young, J. B. & Landsberg, L. (1989). Differential catecholamine responses to dietary intake: effects of macronutrients on dopamine and epinephrine excretion in the rat. Metabolism 38, 9199.CrossRefGoogle ScholarPubMed
Kirk, R. E. (1968). Experimental Design Procedures for the Behavioral Sciences, Belmont, CA: Wadsworth Publishing Company.Google Scholar
Lacy, M. P.,Van Krey, H. P., Skewes, P. A., Denbow, D. M. & Siegel, P. B. (1987). Food intake response of genetically selected high and low-weight line cockerels to plasma infusions from fasted fowl. Poultry Science 66 12241228.CrossRefGoogle ScholarPubMed
Leibowitz, S. F. (1978). Paraventricular nucleus: a primary site for mediating adrenergic stimulation of feeding and drinking. Pharmacology and Biochemistry of Behavior 8, 163175.CrossRefGoogle ScholarPubMed
Leibowitz, S. F., Hammer, N. J. & Chang, K. (1981). Hypothalamic paraventricular nucleus lesions produce overeating and obesity in the rat. Physiology of Behavior 27, 10311040.CrossRefGoogle ScholarPubMed
Leibowitz, S. F. & Shor-Posner, G. (1986). Hypothalamic monoamine systems for control of food intake: analysis of meal patterns and macronutrient selection. In Psycopharmacology of Eating Disorders: Theoretical and Clinical Advances, pp. 2949 [Carobe, M. O. and Blundel, J. E., editors]. New York: Raven Press.Google Scholar
Martin, R. J. & Herbein, J. H. (1976). A comparison of the enzyme levels and in vitro utilization of various substrates for lipogenesis in pair-fed lean and obese pigs. Proceedings of the Society for Experimental Biology and Medicine 151, 231235.CrossRefGoogle ScholarPubMed
Nielsen, J. A., Chapin, D. S., Johnson, J. L. & Torgersen, L. K. (1992). Sertraline, a serotonin-uptake inhibitor, reduces food intake and body weight in lean and genetically obese mice. American Journal of Clinical Nutrition 55, 185S189S.CrossRefGoogle ScholarPubMed
Rosebrough, R. W. & McMurtry, J. P. (1993). Protein and energy relations in the broiler chicken. 11. Effects of protein quantity and quality on metabolism. British Journal of Nutrition 70, 667678.CrossRefGoogle Scholar
Rosebrough, R. W., McMurtry, J. P. & Vasilatos-Younken, R. (1992). Metabolic and hormonal effects of feeding chickens thyroxine and diets containing varied calorie: protein ratios. Nutrition Research 12, 7787.CrossRefGoogle Scholar
Rosebrough, R. W. & Steele, N. C. (1985). Energy and protein relations in the broiler. I. Effect of protein levels and feeding regimes on growth, body composition, and in vitro lipogenesis of broiler chicks. Poultry Science 64, 119126.CrossRefGoogle Scholar
Schwartz, J. H., Young, J. B. & Landsberg, L. (1983). Effect of dietary fat on sympathetic nervous system activity in the rat. Journal of Clinical Investigation 72, 361370.CrossRefGoogle ScholarPubMed
Smith, N. K. & Waldroup, P. W. (1988). Estimation of the tryptophan requirement of male broiler chickens. Poultry Science 67, 11741177.CrossRefGoogle ScholarPubMed
Tackman, J. M., Tews, J. K. & Harper, A. E. (1990). Dietary disproportions of amino acids in the rat: effects on food intake, plasma and brain amino acids and brain serotonin. Journal of Nutrition 120, 521533.CrossRefGoogle ScholarPubMed
Vander Tuig, J. G. & Romsos, D. R. (1984). Effects of dietary carbohydrate, fat, and protein on norepinephrine turnover in rats. Metabolism 33, 2633.CrossRefGoogle ScholarPubMed
Young, J. B., Kaufman, L. N., Savile, M. E. & Landsberg, L. (1985). Increased sympathetic nervous system activity in rats fed a low-protein diet. American Journal of Physiology 248, R267R637.Google ScholarPubMed
Young, J. B. & Landsberg, L. (1977 a). Suppression of sympathetic nervous system during fasting. Science 196, 14731475.CrossRefGoogle ScholarPubMed
Young, J. B. & Landsberg, L. (1977 b). Stimulation of the sympathetic nervous system during sucrose feeding. Nature 269, 615617.CrossRefGoogle ScholarPubMed