Effect of calcium intake and the dietary cation-anion difference during early lactation on the bone mobilization dynamics throughout lactation in dairy cows
Autoři:
Pierre Gaignon aff001; Karine Le Grand aff002; Anca-Lucia Laza-Knoerr aff003; Catherine Hurtaud aff001; Anne Boudon aff001
Působiště autorů:
PEGASE, Agrocampus Ouest, INRA, Saint-Gilles, France
aff001; Phosphea, Dinard, France
aff002; CMI, Saint-Malo Cedex, France
aff003
Vyšlo v časopise:
PLoS ONE 14(11)
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pone.0218979
Souhrn
This study investigated the consequences of a low supply of dietary Ca with or without a low dietary cation-anion difference (DCAD) during early lactation on bone mobilization and reconstitution during lactation and on the dynamics of milk Ca content. Fifteen multiparous Holstein cows were distributed among 3 treatments 5 weeks before their expected calving date. These treatments differed based on the provision of diets through the first 10 weeks of lactation. During this period, the control treatment (NCa) consisted of a diet providing 100% of the Ca requirement, with a DCAD of 200 mEq/kg dry matter (DM). The LCa (low Ca) and LCaLD (low Ca, low DCAD) treatments consisted of diets providing 70% of the Ca requirement, with a DCAD of 200 and 0 mEq/kg DM, respectively. After 10 weeks, all cows received the same total mixed ration, which was formulated to meet 100% of the Ca requirement. LCa and LCaLD tended to decrease the body retention of Ca at 3 weeks of lactation compared with NCa but affected neither the dynamics of the blood biomarkers of bone formation and resorption during lactation nor the body retention of Ca at 17 weeks of lactation. Cows almost entirely compensated for the decrease in Ca supply caused by LCa and LCaLD by increasing their apparent digestive absorption of Ca at 3 weeks of lactation, whereas their apparent digestive absorption was unaffected by the treatments at 17 weeks of lactation. Milk production tended to be lower throughout lactation with LCa and LCaLD compared with NCa, with a mean difference of 2 kg/d. The results of this study also indicated that measuring the dynamics of milk Ca content during lactation cannot be considered effective for indirectly estimating the dynamics of bone mobilization in cows. The results also suggested that limited Ca intake at the beginning of lactation may have deleterious effects on milk production.
Klíčová slova:
Blood – Diet – Fats – Milk – Biomarkers – Casein – Bone resorption
Zdroje
1. Horst RL, Goff JP, Reinhardt TA. Calcium and vitamin D metabolism during lactation. J Mammary Gland Biol Neoplasia. 1997;2: 253–263. doi: 10.1023/a:1026384421273 10882309
2. Horst RL, Goff JP, Reinhardt TA. Adapting to the transition between gestation and lactation: differences between rat, human and dairy cow. J Mammary Gland Biol Neoplasia. 2005;10: 141–156. doi: 10.1007/s10911-005-5397-x 16025221
3. Mundy GR, Guise TA. Hormonal control of calcium homeostasis. Clin Chem. 1999;45: 1347–1352. 10430817
4. Benzie D, Boyne AW, Dalgarno AC, Duckworth J, Hill R, Walker DM. Studies of the skeleton of the sheep I. The effect of different levels of dietary calcium during pregnancy and lactation on individual bones. J Agric Sci. 1955;46: 425–440. doi: 10.1017/S0021859600040491
5. Suttle NF. Mineral Nutrition of Livestock. Cambridge (USA): CABI; 2010.
6. Dixon RM, Kidd LJ, Coates DB, Anderson ST, Benvenutti MA, Fletcher MT, et al. Utilising mobilisation of body reserves to improve the management of phosphorus nutrition of breeder cows. Anim Prod Sci. 2017;57: 2280–2290. doi: 10.1071/AN17324
7. Horst RL. Regulation of calcium and phosphorus homeostasis in the dairy cow. J Dairy Sci. 1986;69: 604–616. doi: 10.3168/jds.S0022-0302(86)80445-3 3517093
8. Reinhardt TA, Horst RL, Goff JP. Calcium, phosphorus, and magnesium homeostasis in ruminants. Vet Clin North Am Food Anim Pract. 1988;4: 331–350. Reinhardt TA, Horst RL, Goff JP. Calcium, phosphorus, and magnesium homeostasis in ruminants. doi: 10.1016/s0749-0720(15)31052-5 3061612
9. Beighle DE. The effect of gestation and lactation on bone calcium, phosphorus and magnesium in dairy cows. J S Afr Vet Assoc. 1999;70: 142–146. doi: 10.4102/jsava.v70i4.782 10855835
10. Ekelund A, Spörndly R, Holtenius K. Influence of low phosphorus intake during early lactation on apparent digestibility of phosphorus and bone metabolism in dairy cows. Livest Sci. 2006;99: 227–236. doi: 10.1016/j.livprodsci.2005.07.001
11. Taylor MS, Knowlton KF, McGilliard ML, Swecker WS, Ferguson JD, Wu Z, et al. Dietary calcium has little effect on mineral balance and bone mineral metabolism through twenty weeks of lactation in Holstein cows. J Dairy Sci. 2009;92: 223–237. doi: 10.3168/jds.2008-1345 19109282
12. Elizondo Salazar JA, Ferguson JD, Beegle DB, Remsburg DW, Wu Z. Body phosphorus mobilization and deposition during lactation in dairy cows. J Anim Physiol Anim Nutr. 2013;97: 502–514. doi: 10.1111/j.1439-0396.2012.01291.x 22452565
13. Puggaard L, Lund P, Liesegang A, Sehested J. Long term effect of reduced dietary phosphorus on feed intake and milk yield in dry and lactating dairy cows. Livest Sci. 2014;159: 18–28. doi: 10.1016/j.livsci.2013.10.009
14. McNeill DM, Roche JR, Stockdale CR, McLachlan BP. Nutritional strategies for the prevention of hypocalcaemia at calving for dairy cows in pasture-based systems. Aust J Agric Res. 2002;53: 755–770. doi: 10.1071/ar01100
15. INRA. Alimentation des bovins, ovins et caprins: besoins des animaux, valeurs des aliments: tables Inra 2010. Paris, France: Editions Quae; 2010.
16. NRC. Nutrient requirements of dairy cattle: Seventh Revised Edition, 2001. Washington (DC): National Academies Press; 2001.
17. AFRC. A reappraisal of the calcium and phosphorus requirements of sheep and cattle. Nutr Abstr Rev. 1991;61: 573–612.
18. Braithwaite GD. Calcium and phosphorus requirements of the ewe during pregnancy and lactation. 1. Calcium. Br J Nutr. 1983;50: 711–722. doi: 10.1079/bjn19830143 6639928
19. Moreira VR, Zeringue LK, Williams CC, Leonardi C, McCormick ME. Influence of calcium and phosphorus feeding on markers of bone metabolism in transition cows. J Dairy Sci. 2009;92: 5189–5198. doi: 10.3168/jds.2009-2289 19762837
20. Wu Z, Satter LD, Blohowiak AJ, Stauffacher RH, Wilson JH. Milk production, estimated phosphorus excretion, and bone characteristics of dairy cows fed different amounts of phosphorus for two or three years. J Dairy Sci. 2001;84: 1738–1748. doi: 10.3168/jds.S0022-0302(01)74609-7 11467824
21. Horst RL, Goff JP, Reinhardt TA, Buxton DR. Strategies for preventing milk fever in dairy cattle. J Dairy Sci. 1997;80: 1269–1280. doi: 10.3168/jds.S0022-0302(97)76056-9 9241589
22. DeGaris PJ, Lean IJ. Milk fever in dairy cows: A review of pathophysiology and control principles. Vet J. 2008;176: 58–69. doi: 10.1016/j.tvjl.2007.12.029 18329301
23. Goff JP, Koszewski NJ. Comparison of 0.46% calcium diets with and without added anions with a 0.7% calcium anionic diet as a means to reduce periparturient hypocalcemia. J Dairy Sci. 2018;101: 5033–5045. doi: 10.3168/jds.2017-13832 29550140
24. INRA. INRA feeding system for ruminants. Wageningen, the Netherlands: Wageningen Academic Publishers; 2018. doi: 10.3920/978-90-8686-292-4
25. Liesegang A, Eicher R, Sassi ML, Risteli J, Kraenzlin M, Riond JL, et al. Biochemical markers of bone formation and resorption around parturition and during lactation in dairy cows with high and low standard milk yields. J Dairy Sci. 2000;83: 1773–1781. doi: 10.3168/jds.S0022-0302(00)75048-X 10984154
26. Anderson ST, Kidd LJ, Benvenutti MA, Fletcher MT, Dixon RM. New candidate markers of phosphorus status in beef breeder cows. Anim Prod Sci. 2017;57: 2291–2303. doi: 10.1071/AN17363
27. VanHouten J, Dann P, McGeoch G, Brown EM, Krapcho K, Neville M, et al. The calcium-sensing receptor regulates mammary gland parathyroid hormone-related protein production and calcium transport. J Clin Invest. 2004;113: 598–608. doi: 10.1172/JCI18776 14966569
28. Gaignon P. Can the dynamic of milk Ca content throughout lactation be an indicator of the effects of management system and diets on bone mobilization in dairy cows?. PhD. Thesis, Agrocampus Ouest. 2018. Available from: https://www.researchgate.net/publication/332466615_Can_the_dynamic_of_milk_Ca_content_throughout_lactation_be_an_indicator_of_the_effects_of_management_system_and_diets_on_bone_mobilization_in_dairy_cows
29. Iwama Y, Kamiya M, Tanaka M, Shioya S. The change of dry matter intake, milk yield and bone turnover in primiparous cows compared to multiparous cows during early lactation. Anim Sci J. 2004;75: 213–218. doi: 10.1111/j.1740-0929.2004.00178.x
30. Horst RL, Goff JP, Reinhardt TA. Advancing age results in reduction of intestinal and bone 1,25-dihydroxyvitamin D receptor. Endocrinology. 1990;126: 1053–1057. doi: 10.1210/endo-126-2-1053 2153518
31. Gaignon P, Gelé M, Hurtaud C, Boudon A. Characterization of the nongenetic causes of variation in the calcium content of bovine milk on French farms. J Dairy Sci. 2018;101: 4554–4569. doi: 10.3168/jds.2017-14043 29501339
32. Seibel MJ. Molecular markers of bone turnover: biochemical, technical and analytical aspects. Osteoporos Int. 2000;11: S18–S29. doi: 10.1007/s001980070003 11193236
33. Pien J. Dosage du phosphore dans le lait. Le Lait. 1969;49: 175–188.
34. Hurtaud C, Rulquin H, Verite R. Effect of Infused Volatile Fatty Acids and Caseinate on Milk Composition and Coagulation in Dairy Cows. J Dairy Sci. 1993;76: 3011–3020. doi: 10.3168/jds.S0022-0302(93)77640-7 8227627
35. SAS Institute. SAS Institute. 2013.
36. Liu S, Rovine MJ, Molenaar PCM. Selecting a linear mixed model for longitudinal data: repeated measures analysis of variance, covariance pattern model, and growth curve approaches. Psychol Methods. 2012;17: 15–30. doi: 10.1037/a0026971 22251268
37. Charbonneau E, Pellerin D, Oetzel GR. Impact of lowering dietary cation-anion difference in, onlactating dairy cows: A meta-analysis. J Dairy Sci. 2006;89: 537–548. doi: 10.3168/jds.S0022-0302(06)72116-6 16428622
38. Goff JP. Macromineral physiology and application to the feeding of the dairy cow for prevention of milk fever and other periparturient mineral disorders. Anim Feed Sci Technol. 2006;126: 237–257. doi: 10.1016/j.anifeedsci.2005.08.005
39. Goff JP, Liesegang A, Horst RL. Diet-induced pseudohypoparathyroidism: A hypocalcemia and milk fever risk factor. J Dairy Sci. 2014;97: 1520–1528. doi: 10.3168/jds.2013-7467 24418271
40. Bushinsky DA. Contribution of intestine, bone, kidney, and dialysis to extracellular fluid calcium content. Clin J Am Soc Nephrol CJASN. 2010;5 Suppl 1: S12–22. doi: 10.2215/CJN.05970809 20089498
41. Van Hulzen KJE, Sprong RC, van der Meer R, van Arendonk J a. M. Genetic and nongenetic variation in concentration of selenium, calcium, potassium, zinc, magnesium, and phosphorus in milk of Dutch Holstein-Friesian cows. J Dairy Sci. 2009;92: 5754–5759. doi: 10.3168/jds.2009-2406 19841235
42. Malacarne M, Franceschi P, Formaggioni P, Sandri S, Mariani P, Summer A. Influence of micellar calcium and phosphorus on rennet coagulation properties of cows milk. J Dairy Res. 2014;81: 129–136. doi: 10.1017/S0022029913000630 24345431
43. Pinto MCX, Kihara AH, Goulart VAM, Tonelli FMP, Gomes KN, Ulrich H, et al. Calcium signaling and cell proliferation. Cell Signal. 2015;27: 2139–2149. doi: 10.1016/j.cellsig.2015.08.006 26275497
44. Wohlt JE, Ritter DE, Evans JL. Calcium Sources for Milk Production in Holstein Cows Via Changes in Dry Matter Intake, Mineral Utilization, and Mineral Source Buffering Potential1. J Dairy Sci. 1986;69: 2815–2824. doi: 10.3168/jds.S0022-0302(86)80735-4 3805457
45. Becker RB, Neal WM, Shealy AL. Effect of calcium-deficient roughages upon milk yield and bone strength in cattle. J Dairy Sci. 1934;17: 1–10. doi: 10.3168/jds.S0022-0302(34)93213-6
46. Caixeta LS, Ospina PA, Capel MB, Nydam DV. Association between subclinical hypocalcemia in the first 3 days of lactation and reproductive performance of dairy cows. Theriogenology. 2017;94: 1–7. doi: 10.1016/j.theriogenology.2017.01.039 28407850
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