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The effects of feeding time and time-restricted feeding on the fattening traits of White Roman geese

Published online by Cambridge University Press:  06 January 2014

S.-Y. Ho ,
Y.-C. Wu ,
Y.-H. Chen  and
S.-K. Yang
S.-Y. Ho
Affiliation:
Department of Animal Science and Biotechnology, Tunghai University, 40704 Taichung, Taiwan
Y.-C. Wu
Affiliation:
Department of Animal Science and Biotechnology, Tunghai University, 40704 Taichung, Taiwan
Y.-H. Chen
Affiliation:
Department of Animal Science and Biotechnology, Tunghai University, 40704 Taichung, Taiwan
S.-K. Yang*
Affiliation:
Department of Animal Science and Biotechnology, Tunghai University, 40704 Taichung, Taiwan
*
† E-mail: [email protected]
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Abstract

This study comprises two trials that investigated the effects of feeding time and time-restricted feeding on the fattening traits and plasma metabolite levels of White Roman geese. In Trial I, 24 geese aged 8 weeks of each sex were allowed free access to a fattening diet for 1 h either in the morning (morning-feeding group) or afternoon (afternoon-feeding group). At 12 weeks of age, blood samples were collected hourly for 4 h, beginning 1 h after feeding to determine the plasma levels of glucose, triacylglycerols and uric acid. The results showed a lower (P<0.05) daily feed intake (DFI) and daily gain (DG) and higher (P<0.05) feed efficiency (FE) for the morning-feeding group compared with those of the afternoon-feeding group. In addition, the postprandial plasma levels of glucose, triacylglycerols and uric acid did not differ (P>0.05) between groups. In Trial II, 12 geese aged 8 weeks of each sex were randomly assigned to either the ad libitum feeding group (control group) or time-restricted feeding group (restricted group). The geese in the control group were fed a fattening diet ad libitum, whereas those in the restricted group were allowed access to the diet for 2 h every morning. All geese were killed at 13 weeks of age and their carcass traits were evaluated. The results showed a lower DFI and DG and higher FE for the restricted group compared with those of the control group (P<0.05). In addition, the restricted group exhibited lower visceral and abdominal fat and higher empty digestive tract and liver weights than those of the control group (P<0.05). The results showed that time-restricted feeding in the morning resulted in superior DG and FE compared with feeding in the afternoon. Moreover, time-restricted feeding implemented in the morning during the fattening period reduced DFI and increased FE in geese compared with ad libitum feeding.

Keywords

carcass traitfatteningfeed efficiencygoosetime-restricted feeding
Type
Full Paper
Information
animal , Volume 8 , Issue 3 , March 2014 , pp. 395 - 400
Copyright
© The Animal Consortium 2014 

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References

Benyi, K and Habi, H 1998. Effects of food restriction during the finishing period on the performance of broiler chickens. British Poultry Science 39, 423–425.CrossRefGoogle ScholarPubMed
Boa-Amponsem, K, Dunnington, EA and Siegel, PB 1991. Genotype, feeding regime and diet interaction in meat chickens. 1. Growth, organ size and feed utilisation. Poultry Science 70, 680–688.CrossRefGoogle Scholar
Chen, YH, Hsu, JC, Shih, BL, Lio, DC and Chen, MT 2003. A study on the optimal marketing age of geese. Journal of the Chinese Society of Animal Science 32, 111–121.Google Scholar
Gidenne, T, Combes, S and Fortun-Lamothe, L 2012. Feed intake limitation strategies for the growing rabbit: effect on feeding behaviour, welfare, performance, digestive physiology and health: a review. Animal 6, 1407–1419.CrossRefGoogle ScholarPubMed
Ho, SY 2010. Effect of feeding system on growth performances and plasma levels of metabolites in White Roman geese. Thesis MS, Tunghai University, Taichung, Taiwan.Google Scholar
Koopmans, SJ, van der Meulen, J, Dekker, R, Corbijn, H and Mroz, Z 2006. Diurnal variation in insulin-stimulated systemic glucose and amino acid utilization in pigs fed with identical meals at 12-hour intervals. Hormone and Metabolic Research 38, 607–613.CrossRefGoogle ScholarPubMed
Kumar, V, Singh, S, Misra, M and Malik, S 2001. Effects of duration and time of food availability on photoperiodic responses in the migratory male blackheaded bunting (Emberiza melanocephala). The Journal of Experimental Biology 204, 2843–2848.CrossRefGoogle ScholarPubMed
Lin, MJ, Chang, SC, Wu, KC, Chen, TF, Jea, TS, Lee, SR and Fan, YK 2007. Feeding value of green napiergrass and nilegrass supplement to diets for white Roman geese. Journal of the Chinese Society of Animal Science 36, 231–242.Google Scholar
Lovatto, PA, Sauvant, D, Noblet, J, Dubois, S and van Milgen, J 2006. Effects of feed restriction and subsequent refeeding on energy utilization in growing pigs. Journal of Animal Science 84, 3329–3336.CrossRefGoogle ScholarPubMed
MacLeod, MG, Tullett, SG and Jewitt, TR 1979. Effect of food intake regulation on the energy metabolism of hens and cockerels of a layer strain. British Poultry Science 20, 521–531.CrossRefGoogle ScholarPubMed
Mittendorfer, B, Patterson, BW and Klein, S 2003. Effect of weight loss on VLDL-triglyceride and apoB-100 kinetics in women with abdominal obesity. American Journal of Physiology – Endocrinology and Metabolism 284, E549–E556.CrossRefGoogle ScholarPubMed
Morgan, PJ, Ross, AW, Mercer, JG and Barrett, P 2003. Photoperiodic programming of body weight through the neuroendocrine hypothalamus. Journal of Endocrinology 177, 27–34.CrossRefGoogle ScholarPubMed
Mullan, BP, Trezona, M, D'Souza, DN and Kim, JC 2009. Effects of continual fluctuation in feed intake on growth performance response and carcass fat-to-lean ratio in grower-finisher pigs. Journal of Animal Science 87, 179–188.CrossRefGoogle ScholarPubMed
Nelson, W, Scheving, L and Halberg, F 1975. Circadian rhythms in mice fed a single daily meal at different stages of lighting regimen. Journal of Nutrition 105, 171–184.CrossRefGoogle ScholarPubMed
Noeske-Hallin, TA, Spieler, RE, Parker, NC, Suttle, MA 1985. Feeding time differentially affects fattening and growth of channel catfish. Journal of Nutrition 115, 1228–1232.CrossRefGoogle ScholarPubMed
NRC 1994. Nutrient requirements of poultry, 9th edition. National Academy Press, Washington, DC, USA.Google Scholar
Ocak, N and Sivri, F 2008. Liver colourations as well as performance and digestive tract characteristics of broilers may change as influenced by stage and schedule of feed restriction. Journal of Animal Physiology and Animal Nutrition (Berlin) 92, 546–553.CrossRefGoogle ScholarPubMed
Philippens, KMH, Von Mayersbach, H and Scheving, LE 1977. Effects of the scheduling of meal-feeding at different phases of the circadian system in rats. Journal of Nutrition 107, 176–193.CrossRefGoogle ScholarPubMed
Rashotte, ME, Basco, PS and Henderson, RP 1995. Daily cycles in body temperature, metabolic rate, and substrate utilization in pigeons: influence of amount and timing of food consumption. Physiology and Behavior 57, 731–746.CrossRefGoogle ScholarPubMed
Scheving, LE, Tsai, TH and Scheving, LA 1983. Chronobiology of the intestinal tract of the mouse. American Journal of Anatomy 168, 433–465.CrossRefGoogle ScholarPubMed
Su, G, Sorensen, P and Kestin, SC 1999. Meal feeding is more effective than early feed restriction at reducing the prevalence of leg weakness in broiler chickens. Poultry Science 78, 949–955.CrossRefGoogle ScholarPubMed
Sundararaj, BI, Nath, P and Halberg, F 1982. Circadian meal timing in relation to lighting schedule optimizes catfish body weight gain. Journal of Nutrition 112, 1085–1097.CrossRefGoogle ScholarPubMed
Svihus, B, Sacranie, A, Denstadli, V and Choct, M 2010. Nutrient utilization and functionality of the anterior digestive tract caused by intermittent feeding and inclusion of whole wheat in diets for broiler chickens. Poultry Science 89, 2617–2625.CrossRefGoogle ScholarPubMed