Register      Login
Animal Production Science Animal Production Science Society
Food, fibre and pharmaceuticals from animals
RESEARCH ARTICLE (Open Access)

Dietary calcium supplementation affects nutrient digestibility and antler-production performance during the antler-velvet growth period of male sika deer

Weili Sun A * , Haiping Zhao A * , Kun Bao A , Chunyi Li A and Guangyu Li A B
+ Author Affiliations
- Author Affiliations

A Institute of Special Animal and Plant Sciences, Chinese Academy of Agriculture Sciences, Jilin Provincial Key Laboratory for Molecular Biology of Special Economic Animals, No. 4899, Juye Street, Jingyue District, Changchun City, Jilin Province 130112, China.

B Corresponding author. Email: tcslgy@126.com

Animal Production Science 59(9) 1689-1695 https://doi.org/10.1071/AN17862
Submitted: 11 December 2017  Accepted: 29 October 2018   Published: 25 January 2019

Journal Compilation © CSIRO 2019 Open Access CC BY-NC-ND

Abstract

Effects of calcium (Ca) supplementation on nutrient digestibility, physiochemical characteristics and antler growth in farmed male sika deer were investigated. Eighteen sika deer (6 years old, 105.50 ± 5.05 kg) were assigned into the following three treatments where they had ad libitum access to water for 90 days: (1) control (C), basal diet containing 0.5% Ca; (2) Ca1.10, basal diet supplemented with 0.6% Ca; and (3) Ca1.70, basal diet supplemented with 1.2% Ca. The basal diet contained 0.50% Ca and 0.34% phosphorus (P). Each group consisted of the same ratio of Ca to P (provided as CaCO3 and CaHPO4). The results showed that the digestibility of dry matter (DM) and crude protein in the Ca1.70 group was lower than in the other two groups. The digestibilities of Ca, P and neutral detergent fibre in the Ca1.10 group were higher than those in the C group and Ca1.70 group (P < 0.05). Concentrations of Ca and P in faeces increased with an increasing supplementation level of Ca and the highest concentrations were observed in the Ca1.70 group (P < 0.05). There were no differences in the concentrations of parathyroid hormone, alkaline phosphatase and osteocalcin among the treatments. Testosterone and oestradiol concentrations of the Ca1.7 group were higher than those of the C and Ca1.10 groups (P < 0.05). Average daily gains of fresh antler weight and dry antler weight of the groups Ca1.10 and Ca1.70 were greater than those of the C (P < 0.05). Fresh and dry antler yields of the Ca1.10 group were higher than those of the other groups (P < 0.05). In conclusion, optimal level of Ca supplement was found to be total Ca concentration of 1.10–1.70%, on the basis of DM, which significantly increased feed digestibility and antler daily gain for the 6-year-old sika deer.

Additional keywords: antler growth, Ca, P.


References

Anke M, Groppel B, Reissig W, Ludke H, Grun M, Dittrich G (1973) Manganese deficiency in ruminants. 3. Disorders of reproduction, skeleton and nerves caused by manganese deficiency in female ruminants and their progeny. Archiv fur Tierernahrung 23, 197–211.
Manganese deficiency in ruminants. 3. Disorders of reproduction, skeleton and nerves caused by manganese deficiency in female ruminants and their progeny.Crossref | GoogleScholarGoogle Scholar | 4731545PubMed |

AOAC International (2005) ‘Official methods of analysis of AOAC International.’ 18th edn. (AOAC International: Gaithersburg, MD)

Bain SD, Watkins BA (1993) Local modulation of skeletal growth and bone modeling in poultry. The Journal of Nutrition 123, 317–322.
Local modulation of skeletal growth and bone modeling in poultry.Crossref | GoogleScholarGoogle Scholar | 8429381PubMed |

Banks WJ, Epling GP, Kainer RA, Davis RW (1968) Antler growth and osteoporosis. II. Gravimetric and chemical changes in the costal compacta during the antler growth cycle. The Anatomical Record 162, 399–405.
Antler growth and osteoporosis. II. Gravimetric and chemical changes in the costal compacta during the antler growth cycle.Crossref | GoogleScholarGoogle Scholar | 5701620PubMed |

Borsy A, Podani J, Steger V, Balla B, Horvath A, Kosa JP, Gyurjan I, Molnar A, Szabolcsi Z, Szabo L, Jako E, Zomborszky Z, Nagy J, Semsey S, Vellai T, Lakatos P, Orosz L (2009) Identifying novel genes involved in both deer physiological and human pathological osteoporosis. Molecular Genetics and Genomics Mgg 281, 301–313.
Identifying novel genes involved in both deer physiological and human pathological osteoporosis.Crossref | GoogleScholarGoogle Scholar | 19107525PubMed |

Bronner F (1987) Intestinal Ca absorption: mechanisms and applications. The Journal of Nutrition 117, 1347–1352.
Intestinal Ca absorption: mechanisms and applications.Crossref | GoogleScholarGoogle Scholar | 3305814PubMed |

Brown RD (1990) Horns, pronghorns, and antler. In ‘Nutrition and antler development’. (Eds GA Bubenik, AB Bubenik) pp. 426–441. (Springer-Verlag: New York)

Chapman DI (1975) Antler-bone of contention. Mammal Review 5, 121–172.
Antler-bone of contention.Crossref | GoogleScholarGoogle Scholar |

Chen Y, Li FT, Qian DW, Jiang Q, Duan JA (2014) Analysis and evaluation of red deer horn and the plum blossom antlers off dish in inorganic element. Chinese Traditional Patent Medicine 36, 2577–2582.

Chu HP (2005) ‘Study on optimum supply of calcium and phosphorus in dairy cows.’ Master’s Thesis. College of Animal Science and Technology, Shandong Agricultural University, Taian City.

Chu HP, Wang ZH, Li FC (2010) Effects of dietary Ca level on Ca metabolism in lactating dairy cows. Chinese Journal of Animal Nutrition 22, 1286–1292. [in Chinese]

French CE, Mcewen LC, Magruder ND, Ingram RH, Swift RW (1956) Nutrient requirements for growth and antler development in the white-tailed deer. The Journal of Wildlife Management 20, 221–232.
Nutrient requirements for growth and antler development in the white-tailed deer.Crossref | GoogleScholarGoogle Scholar |

Grasman BT, Hellgren EC (1993) Phosophorus nutrition in white-tailed deer: nutrition balance, physiological responses, and antler growth. Ecology 74, 2279–2296.
Phosophorus nutrition in white-tailed deer: nutrition balance, physiological responses, and antler growth.Crossref | GoogleScholarGoogle Scholar |

Hillman JR, Davis RW, Abdelbaki YZ (1973) Cyclic bone remodeling in deer. Calcified Tissue Research 12, 323–330.
Cyclic bone remodeling in deer.Crossref | GoogleScholarGoogle Scholar | 4746698PubMed |

Huang J, Zhang TT, Bao K, Li GY, Wang KY (2015) Effect of supplementation of lysine and methionine on growth performance, nutrients digestibility and serum biochemical indices for growing sika deer (Cervus nippon) fed protein deficient diet. Italian Journal of Animal Science 14, 60–65.
Effect of supplementation of lysine and methionine on growth performance, nutrients digestibility and serum biochemical indices for growing sika deer (Cervus nippon) fed protein deficient diet.Crossref | GoogleScholarGoogle Scholar |

Landete-Castillejos T, Garcia A, Gallego L (2007) Body weight, early growth and antler size influence antler bone mineral composition of Iberian red deer (Cervus elaphus hispanicus). Bone 40, 230–235.
Body weight, early growth and antler size influence antler bone mineral composition of Iberian red deer (Cervus elaphus hispanicus).Crossref | GoogleScholarGoogle Scholar | 16949898PubMed |

Li C, Suttie JM (1996) Histological examination of the antlerogenic region of red deer (Cervus elaphus) hummels. New Zealand Veterinary Journal 44, 126–130.
Histological examination of the antlerogenic region of red deer (Cervus elaphus) hummels.Crossref | GoogleScholarGoogle Scholar | 16031913PubMed |

Li CY, Littlejohn RP, Suttie JM (1999) Effects of insulin-like growth factor 1 and testosterone on the proliferation of antlerogenic cells in vitro. Journal of Experimental Zoology 284, 82–90.
Effects of insulin-like growth factor 1 and testosterone on the proliferation of antlerogenic cells in vitro.Crossref | GoogleScholarGoogle Scholar |

Li CY, Yang FH, Sheppard A (2009) Adult stem cells and mammalian epimorphic regeneration-insights from studying annual renewal of deer antlers. Current Stem Cell Research & Therapy 4, 237–251.
Adult stem cells and mammalian epimorphic regeneration-insights from studying annual renewal of deer antlers.Crossref | GoogleScholarGoogle Scholar |

Magruder ND, French CE, McEwen LC, Swift RW (1957) ‘Nutritional requirements of White-tailed deer for growth and antler development II.’ Bulletin 628. Pennsylvania State University, College of Agriculture, Agricultural Experiment Station.

Moen R, Pastor J (1996) Simulating antler growth and energy, nitrogen, calcium and phosphorus metabolism in caribou. In ‘The seventh North American caribou conference’, 19–21 August 1996, Thunder Bay, Ontario, Canada.

Muir PD, Sykes AR, Barrell GK (1987) Growth and mineralization of antlets in red deer (Cervus elaphbus). New Zealand Journal of Agricultural Research 30, 305–315.
Growth and mineralization of antlets in red deer (Cervus elaphbus).Crossref | GoogleScholarGoogle Scholar |

Schneider A (1985) Eruptive processes, mineralization and isotopic evolution of the Los Frailes Karikari region/Bolivia. Chemistry (Weinheim an der Bergstrasse, Germany) 16, 13330–13334.

Stéger V, Molnar A, Borsy A, Gyurjan I, Szabolcsi Z, Dancs G, Molnar J, Papp P, Nagy J, Puskas L, Barta E, Zomborszky Z, Horn P, Podani J, Semsey S, Lakatos P, Orosz L (2010) Antler development and coupled osteoporosis in the skeleton of red deer Cervus elaphus: expression dynamics for regulatory and effector genes. Molecular Genetics and Genomics 284, 273–287.
Antler development and coupled osteoporosis in the skeleton of red deer Cervus elaphus: expression dynamics for regulatory and effector genes.Crossref | GoogleScholarGoogle Scholar | 20697743PubMed |

Wu FF, Li HQ, Jin LJ, Li XY, Ma YS, You JS, Li SY, Xu YP (2013) Deer antler base as a traditional Chinese medicine: a review of its traditional uses, chemistry and pharmacology. Journal of Ethnopharmacology 145, 403–415.
Deer antler base as a traditional Chinese medicine: a review of its traditional uses, chemistry and pharmacology.Crossref | GoogleScholarGoogle Scholar |