Hostname: page-component-cd9895bd7-jn8rn Total loading time: 0 Render date: 2024-12-27T11:33:02.888Z Has data issue: false hasContentIssue false

Consequences of dietary calcium and phosphorus depletion and repletion feeding sequences on growth performance and body composition of growing pigs

Published online by Cambridge University Press:  25 October 2017

E. Gonzalo
Affiliation:
Département de Sciences Animales, Université Laval, 2425 rue de l’Agriculture, ville de Québec, QC, Canada G1V 0A6 Dairy and Swine Research and Development Centre, Agriculture and Agri-Food Canada, 2000 College Street, Sherbrooke, QC, Canada J1M 1Z3
M. P. Létourneau-Montminy
Affiliation:
Département de Sciences Animales, Université Laval, 2425 rue de l’Agriculture, ville de Québec, QC, Canada G1V 0A6
A. Narcy
Affiliation:
Unités de Recherches Avicoles, INRA, UR83, 37380 Nouzilly, Centre-Val de Loire, France
J. F. Bernier
Affiliation:
Département de Sciences Animales, Université Laval, 2425 rue de l’Agriculture, ville de Québec, QC, Canada G1V 0A6
C. Pomar*
Affiliation:
Dairy and Swine Research and Development Centre, Agriculture and Agri-Food Canada, 2000 College Street, Sherbrooke, QC, Canada J1M 1Z3
*
Get access

Abstract

The effect of a calcium (Ca) and phosphorus (P) depletion and repletion strategy was studied in four consecutive feeding phases of 28 days each. In all, 60 castrated male pigs (14±1.6 kg initial BW) received 60% (low (L) diet; depletion) or 100% (control (C) diet; repletion) of their Ca and digestible P requirements according to six feeding sequences (CCCC, CCCL, CLCC, CCLC, LCLC and LLLL; subsequent letters indicate the diet received in phases 1, 2, 3 and 4, respectively). Pigs bone mineral content in whole-body (BMCb) and lumbar vertebrae L2 to L4 (BMCv) was measured in every feeding phase by dual-energy X-ray absorptiometry. Growth performance was slightly (<10%) affected by depletion, however, dietary treatments did not affect overall growth. Compared with control pigs, depletion reduced BMCb (34%, 38%, 33% and 22%) and BMCv (46%, 54%, 38% and 26%) in phases 1 to 4, respectively. Depletion increased however digestible P retention efficiency from the second to the fourth phases allowing LLLL pigs to present no differences in BMCb and BMCv gain compared with CCCC pigs in phase 4. Growth performance in repleted compared with control pigs was lower in phase 2, was no different in phase 3 and was lower in CLCC pigs in phase 4. Repletion increased body P and Ca retention efficiency when compared with control pigs (respectively, 8% and 10% for LC v. CC, P<0.01; 8% and 10% for CLC v. CCC, P<0.10; 18% and 25% for CLCC, CCLC, LCLC v. CCCC, P<0.001). Moreover, BMCv gain was higher in CLC pigs (P<0.001) and gains of body P, Ca, BMCb and BMCv in phase 4 were also higher in repleted than in CCCC pigs (respectively, 14%, 20%, 20% and 52%; P⩽0.02). Repletion reduced body P, Ca, BMCb and BMCv masses in phase 2 but no differences were found in phase 4 compared with control pigs. Lumbar vertebrae L2 to L4 bone mineral content was more sensitive to depletion and repletion sequences than BMCb especially in the first phase probably due to a higher proportion of metabolically active trabecular bone in vertebrae than in the whole skeleton. Dietary Ca was, however, oversupply in L compared with C diets (3.1 v. 2.5 Ca:digestible P ratio, respectively) suggesting that P has probably driven the regulations. Phosphorus and Ca depletion and repletion increases dietary P utilization efficiency and can help to reduce dietary P supply, but the underlying mechanisms need elucidation before its practical application.

Type
Research Article
Copyright
© The Animal Consortium 2017 and Her Majesty the Queen in Right of Canada, represented by the Minister of Agriculture and Agri-Food Canada and the Minister of Health Canada 

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

Agriculture and Agri-Food Canada 2012. Recommended code of practice for the care and handling of farm animals: Pigs. AAFC Publication, Ottawa, Ontario, Canada.Google Scholar
Aiyangar, AK, Au, AG, Crenshaw, TD and Ploeg, HL 2010. Recovery of bone strength in young pigs from an induced short-term dietary calcium deficit followed by a calcium replete diet. Medical Engineering and Physics 32, 11161123.CrossRefGoogle ScholarPubMed
Alexander, LS, Qu, A, Cutler, SA, Mahajan, A, Lonergan, SR, Rothschild, MF, Weber, TE, Kerr, BJ and Stahl, CH 2008. Response to dietary phosphorus deficiency is affected by genetic background in growing pigs. Journal of Animal Science 86, 25852595.Google Scholar
Association of Official Analytical Chemists 1990. Official methods of analysis, 15th edition. AOAC, Arlington, VA, USA.Google Scholar
Brautbar, N, Lee, DN, Coburn, JW and Kleeman, CR 1979. Normophosphatemic phosphate depletion in growing rat. American Journal of Physiology 236, 283288.Google ScholarPubMed
Bullock, J, Boyle, J and Wang, MB 2001. NMS physiology Volume 578, 4th edition. Lippincott Williams & Wilkins, Philadelphia, PA, USA.Google Scholar
Canadian Council of Animal Care 2009. CCAC guidelines on: the care and use of farm animals in research, teaching and testing. CCAC, Ottawa, Ontario, Canada.Google Scholar
Clarke, B 2008. Normal bone anatomy and physiology. Clinical Journal of the American Society of Nephrology 3, 131139.Google Scholar
Cordell, D, Drangert, JO and White, S 2009. The story of phosphorus: global food security and food for thought. Global Environmental Change 19, 292305.Google Scholar
Crenshaw, TD 2001. Calcium, phosphorus, vitamin D, and vitamin K in swine nutrition. In Swine nutrition, 2nd edition (ed. AJ Lewis and LL Southern), pp. 187212. CRC Press, Boca Raton, FL, USA.Google Scholar
Dritz, SS, Tokach, MD, Sargeant, JM, Goodband, RD and Nelssen, JL 2000. Lowering dietary phosphorus results in a loss in carcass value but not decreased growth performance. Swine Health and Production 8, 121124.Google Scholar
Ekpe, ED, Zijlstra, RT and Patience, JF 2002. Digestible phosphorus requirement of grower pigs. Canadian Journal of Animal Science 82, 541549.Google Scholar
Gutzwiller, A, Hess, HD, Adam, A, Guggisberg, D, Liesegang, A and Stoll, P 2011. Effects of a reduced calcium, phosphorus and protein intake and of benzoic acid on calcium and phosphorus metabolism of growing pigs. Animal Feed Science and Technology 168, 113121.Google Scholar
Jondreville, C and Dourmad, JY 2005. Le phosphore dans la nutrition des porcs. INRA Productions Animales 18, 183192.Google Scholar
Kim, C and Park, D 2013. The effect of restriction of dietary calcium on trabecular and cortical bone mineral density in the rats. Journal of Exercise Nutrition & Biochemistry 17, 123131.CrossRefGoogle ScholarPubMed
Létourneau-Montminy, MP, Jondreville, C, Sauvant, D and Narcy, A 2012. Meta-analysis of phosphorus utilization by growing pigs: effect of dietary phosphorus, calcium and exogenous phytase. Animal 6, 15901600.Google Scholar
Létourneau-Montminy, MP, Lovatto, PA and Pomar, C 2014. Apparent total tract digestibility of dietary calcium and phosphorus and their efficiency in bone mineral retention are affected by body mineral status in growing pigs. Journal of Animal Science 92, 39143924.Google Scholar
Létourneau-Montminy, MP, Narcy, A, Dourmad, JY, Crenshaw, TD and Pomar, C 2015. Modeling the metabolic fate of dietary phosphorus and calcium and the dynamics of body ash content in growing pigs. Journal of Animal Science 93, 12001217.Google Scholar
Nielsen, AJ 1973. Anatomical and chemical composition of Danish Landrace pigs slaughtered at 90 kilograms live weight in relation to litter, sex and feed composition. Journal of Animal Science 36, 476483.Google Scholar
National Research Council 2012. Nutrient requirements of swine. National Academy Press, Washington, DC, USA.Google Scholar
Ryan, WF, Lynch, PB and O’Doherty, JV 2011. Compensatory effect of dietary phosphorus on performance of growing pigs and development of bone mineral density assessed using dual energy X-ray absorptiometry. Livestock Science 138, 8995.Google Scholar
Saddoris, KL, Fleet, JC and Radcliffe, JS 2010. Sodium-dependent phosphate uptake in the jejunum is post-transcriptionally regulated in pigs fed a low-phosphorus diet and is independent of dietary calcium concentration. Journal of Nutrition 140, 731736.CrossRefGoogle ScholarPubMed
Sauvant, D, Perez, JM and Tran, G 2004. Tables de composition et de valeur nutritive des matières premières destinées aux animaux d’élevage: Porcs, volailles, bovins, ovins, caprins, lapins, chevaux, poissons. Éditions INRA, Paris, France.Google Scholar
Schanler, RJ, Abrams, SA and Sheng, HP 1991. Calcium and phosphorus deficiencies affect mineral distribution in neonatal miniature piglets. The American Journal of Clinical Nutrition 54, 420424.Google Scholar
Schröder, B, Breves, G and Rodehutscord, M 1996. Mechanisms of intestinal phosphorus absorption and availability of dietary phosphorus in pigs. Deutsche Tierärztliche Wochenschrift 103, 209214.Google Scholar
Suttle, NF 2010. Mineral nutrition of livestock, 4th edition. CABI Publishing, Wallingford, Oxfordshire, UK.CrossRefGoogle Scholar
Underwood, EJ and Mertz, W 1987. Introduction. In Trace elements in human and animal nutrition, 5th revised edition (ed. W Mertz), pp. 119. Academic Press, New York, NY, USA.Google Scholar
Varley, PF, Sweeney, T, Ryan, MT and O’Doherty, JV 2011. The effect of phosphorus restriction during the weaner-grower phase on compensatory growth, serum osteocalcin and bone mineralization in gilts. Livestock Science 135, 282288.Google Scholar
Xu, H, Bai, L, Collins, JF and Ghishan, FK 2002. Age-dependent regulation of rat intestinal type IIb sodium-phosphate cotransporter by 1,25-(OH)2 vitamin D3 . American Journal Physiology and Cellular Physiology 282, C487C493.Google Scholar