Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-26T20:38:45.400Z Has data issue: false hasContentIssue false

Influence of salbutamol administered as the single active enantiomer (R-salbutamol) on the growth performance and carcass characteristics of broiler chickens

Published online by Cambridge University Press:  18 August 2016

J. P. Fawcett
Affiliation:
School of Pharmacy, University of Otago, Dunedin, New Zealand
V. Ravindran*
Affiliation:
Institute of Food, Nutrition and Human Health, Massey University, Palmerston North, New Zealand
P. C. H. Morel
Affiliation:
Institute of Food, Nutrition and Human Health, Massey University, Palmerston North, New Zealand
M. Zhang
Affiliation:
School of Pharmacy, University of Otago, Dunedin, New Zealand
V. B. Ciofalo
Affiliation:
Bridge Pharma, Inc., 902 Contento Street, Sarasota, Florida 34242, USA
C. B. Spainhour
Affiliation:
Bridge Pharma, Inc., 902 Contento Street, Sarasota, Florida 34242, USA
G. Aberg
Affiliation:
Bridge Pharma, Inc., 902 Contento Street, Sarasota, Florida 34242, USA
*
Corresponding author. E-mail:[email protected]
Get access

Abstract

Salbutamol (albuterol) is a β-adrenergic agonist marketed as a racemic (50: 50) mixture of R- and S-enantiomers (rac-salbutamol). Since only R-salbutamol is pharmacologically active and S-salbutamol has a longer half-life in humans, we examined R-salbutamol as a performance enhancer and repartitioning agent in domestic chickens. The effects of feeding diets containing R-salbutamol (5, 10 and 15 mg/kg diet) and rac-salbutamol (10 mg/kg diet) from day 21 to 42 post hatching on growth performance, carcass characteristics and tissue concentrations of R- and S-salbutamol in male and female broilers were compared with a control diet. R-salbutamol in the diet lowered the weight gains in both sexes, but the magnitude of reduction was greater in males as indicated by a significant R-salbutamol ✕ gender interaction. R-salbutamol also lowered food intake and improved food conversion ratios in both sexes. The relative weights of breast muscle and leg muscle were significantly increased and the relative weight of the fat pad was significantly decreased in birds of both sexes given diets containing R-salbutamol. Carcass protein content increased and carcass fat content decreased but the differences were not statistically significant. A significant dose-response effect was observed for tissue concentrations of R-salbutamol in all tissues, except the fat. Performance and carcass parameters in chickens given the 5 mg/kg R-salbutamol diet were similar to those given the 10 mg/kg rac-salbutamol diet, but tissue concentrations of R-salbutamol were lower. Chickens given the 10 mg/ kg rac-salbutamol diet had higher tissue concentrations of salbutamol than chickens given the 10 mg/kg R-salbutamol diet and higher concentrations of S-salbutamol than R-salbutamol in liver and leg muscle. Overall, these results demonstrate that R-salbutamol is an effective repartitioning agent in broiler chickens.

Type
Growth, development and meat science
Copyright
Copyright © British Society of Animal Science 2004

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Association of Official Analytical Chemists. 1990. Official methods of analysis, 15th edition. AOAC, Washington, DC.Google Scholar
Bardsley, R. G., Allcock, S. M. J., Dawson, J. M., Dumelow, N. W., Higgins, J. A., Lasslett, Y. V., Lockley, A. K., Parr, T. and Buttery, P. J. 1992. Effect of ß-agonists on expression of calpain and calpastatin activity in skeletal muscle. Biochimie 74: 267273.CrossRefGoogle Scholar
Boulton, D. W. and Fawcett, J. P. 1995. Determination of salbutamol enantiomers in human plasma and urine by chiral high-performance liquid chromatography. Journal of Chromatography B 672: 103109.Google Scholar
Boulton, D. W. and Fawcett, J. P. 1996. Enantioselective disposition of salbutamol in man following oral and intravenous administration. British Journal of Clinical Pharmacology 41: 3540.Google Scholar
Boulton, D. W. and Fawcett, J. P. 1997. Pharmacokinetics and pharmacodynamics of single oral doses of albuterol and its enantiomers in humans. Clinical Pharmacology and Therapeutics 62: 138144.CrossRefGoogle ScholarPubMed
Cole, D. J. A., Wood, J. D. and Kilpatrick, M. J. 1987. Effects of the beta-agonist GAH/034 (salbutamol) on growth, carcass quality and meat quality of pigs. In Beta-agonists and their effects on animal growth and carcass quality (ed. Hanrahan, J. P.), p. 137. Elsevier Applied Science, New York.Google Scholar
Duquett, P. F. and Muir, L. 1982. Effect of the beta-adrenergic agonists isoproterenol, clenbuterol, L-640, 033 and BRL 35135 on lipolysis and lipogenesis in rat adipose tissue in vitro . Journal of Animal Science 46: 310321.Google Scholar
Malucelli, A., Ellendorff, F. and Meyer, H. H. D. 1994. Tissue distribution and residues of clenbuterol, salbutamol, and terbutaline in tissues of treated broiler chickens. Journal of Animal Science 72: 15551560.CrossRefGoogle ScholarPubMed
Mazzanti, G., Daniele, C., Boatto, G., Manca, G., Brambilla, G. and Loizzo, A. 2003. New beta-adrenergic agonists used illicitly as growth promoters in animal breeding: chemical and pharmacodynamic studies. Toxicology 187: 9199.CrossRefGoogle ScholarPubMed
Moloney, A., Allen, P., Joseph, R. and Tarrant, V. 1991. Influence of beta-adrenergic agonists and similar compounds on growth. In Growth regulation in farm animals (ed. Pearson, A. M. and Dutson, T. R.), pp. 455513. Elsevier, New York.Google Scholar
Moody, D. E., Hancock, D. L. and Anderson, D. B. 2000. Phenethanolamine repartitioning agents. In Farm animal metabolism and nutrition (ed. D’Mello, J. P. F.), pp. 6596. CAB International, Wallingford.Google Scholar
National Research Council. 1990. Metabolic modifiers – effects on the nutrient requirements of food-producing animals. National Academy of Sciences, Washington, DC.Google Scholar
National Research Council. 1994. Nutrient requirements of domestic animals. Nutrient requirements of poultry. National Academy Press, Washington, DC.Google Scholar
Reeds, P. J., Hay, S. M., Dorwood, P. M. and Palmer, R. M. 1986. Stimulation of muscle growth by clenbuterol: lack of effect on muscle protein biosynthesis. British Journal of Nutrition 56: 249258.CrossRefGoogle ScholarPubMed
Rehfeldt, C., Schadereit, R., Weikard, R. and Reichel, K. 1997. Effect of clenbuterol on growth, carcase and skeletal muscle characteristics in broiler chickens. British Poultry Science 38: 366373.CrossRefGoogle ScholarPubMed
Smith, D. J. 1998. The pharmacokinetic, metabolism, and tissue residues of β-adrenergic agonists in livestock. Journal of Animal Science 76: 173194.Google Scholar
Statistical Analysis Systems Institute. 1997. SAS/STAT® user’s guide: statistics, version 6•12. SAS Institute Inc., Cary, NC.Google Scholar
Warriss, P. D., Kestin, S. C., Rolph, T. P. and Brown, S. N. 1990. The effects of the beta-adrenergic agonist salbutamol on meat quality in pigs. Journal of Animal Science 68: 128.Google Scholar
Warriss, P. D., Nute, G. R., Rolph, T. P., Brown, S. N. and Kestin, S. C. 1991. Eating quality of meat from pigs given the beta-adrenergic agonist salbutamol. Meat Science 30: 7580.Google Scholar
Wellenreiter, R. H. 1991. β-adrenergic agonists for poultry. Critical Reviews in Poultry Biology 3: 229237.Google Scholar