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Impacts of CLA and dietary concentrate proportion on blood metabolite concentration and proliferation of peripheral blood mononuclear cells of periparturient dairy cows

Published online by Cambridge University Press:  10 November 2014

M. Petzold
Affiliation:
Institute of Animal Nutrition, Friedrich-Loeffler-Institute (FLI), Federal Research Institute for Animal Health, 38116 Braunschweig, Germany
U. Meyer*
Affiliation:
Institute of Animal Nutrition, Friedrich-Loeffler-Institute (FLI), Federal Research Institute for Animal Health, 38116 Braunschweig, Germany
S. Kersten
Affiliation:
Institute of Animal Nutrition, Friedrich-Loeffler-Institute (FLI), Federal Research Institute for Animal Health, 38116 Braunschweig, Germany
J. Spilke
Affiliation:
Institute of Agricultural and Nutritional Sciences, Biometrics and Informatics in Agriculture Group, Martin-Luther University Halle-Wittenberg, 06120 Halle (Saale), Germany
G. Breves
Affiliation:
Department of Physiology, University of Veterinary Medicine, 30173 Hannover, Germany
S. Dänicke
Affiliation:
Institute of Animal Nutrition, Friedrich-Loeffler-Institute (FLI), Federal Research Institute for Animal Health, 38116 Braunschweig, Germany
*
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Abstract

The study aimed to examine effects of supplemented CLA to periparturient dairy cows receiving different concentrate proportions antepartum (a.p.) to investigate CLA effects on metabolism and immune function. Compared with adapted feeding, high-concentrate diet a.p. should induce a ketogenic metabolic situation postpartum (p.p.) to better understand how CLA works. A total of 64 pregnant German Holstein cows had ad libitum access to partial mixed rations based on concentrate and roughage 3 weeks before calving until day 60 p.p. A.p., cows received 100 g/day control fat (CON) or a CLA supplement, either in a low-concentrate (20%, CON-20, CLA-20) or high-concentrate diet (60%, CON-60, CLA-60). P.p., concentrate proportion was adjusted to 50% while fat supplementation continued. After day 32 p.p., half of the animals of CLA-groups changed to CON supplementation (CLA-20-CON, CLA-60-CON). A ketogenic metabolic state p.p. was not achieved and respective impacts of CLA could not be examined. Blood samples for isolation of peripheral blood mononuclear cells (PBMC) were collected on day −21, 7, 28 and 56 relative to calving. Blood chemistry samples were taken over the entire experimental period. Mitogen-stimulated proliferation of PBMC remained unaffected. Besides serum concentrations of triglycerides, total bilirubin, total protein, albumin and IGF-1, clinical-chemical serum characteristics remained uninfluenced by treatments. No post-supplementation effect could be observed. Measured blood metabolites and mitogen-stimulated proliferation of PBMC indicate that all groups had an increased metabolic stress around calving, whereby group CLA-20 was affected more severely. Overall, supplemented CLA did not positively affect metabolism or immune function of periparturient dairy cows. However, feeding CLA in a low-concentrate diet a.p. seems to increase liver stress around calving via reduced DMI.

Type
Research Article
Copyright
© The Animal Consortium 2014 

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References

Balogh, OG, Febel, H, Huszenicza, G, Kulcsar, M, Abonyi-Toth, Z, Endrodi, T and Gabor, G 2012. Seasonal fertility differences in synchronised dairy cows: ultrasonic, metabolic and endocrine findings. Acta Veterinaria Hungarica 60, 131143.Google Scholar
Baumgard, LH, Corl, BA, Dwyer, DA and Bauman, DE 2002. Effects of conjugated linoleic acids (CLA) on tissue response to homeostatic signals and plasma variables associated with lipid metabolism in lactating dairy cows. Journal of Animal Science 80, 12851293.Google Scholar
Baumgard, LH, Corl, BA, Dwyer, DA, Saebo, A and Bauman, DE 2000. Identification of the conjugated linoleic acid isomer that inhibits milk fat synthesis. American Journal of Physiology, Regulatory, Integrative and Comparative Physiology 278, R179R184.CrossRefGoogle ScholarPubMed
Bernal-Santos, G, Perfield, JW 2nd, Barbano, DM, Bauman, DE and Overton, TR 2003. Production responses of dairy cows to dietary supplementation with conjugated linoleic acid (CLA) during the transition period and early lactation. Journal of Dairy Science 86, 32183228.Google Scholar
Bostedt, H 1974. Enzyme activity in the blood serum of cows during the period before and after parturition. Berliner und Muenchener Tieraerztliche Wochenschrift 87, 365371.Google Scholar
Castaneda-Gutierrez, E, Overton, TR, Butler, WR and Bauman, DE 2005. Dietary supplements of two doses of calcium salts of conjugated linoleic acid during the transition period and early lactation. Journal of Dairy Science 88, 10781089.CrossRefGoogle ScholarPubMed
Dänicke, S, Kowalczyk, J, Renner, L, Pappritz, J, Meyer, U, Kramer, R, Weber, EM, Döll, S, Rehage, J and Jahreis, G 2012. Effects of conjugated linoleic acids fed to dairy cows during early gestation on hematological, immunological, and metabolic characteristics of cows and their calves. Journal of Dairy Science 95, 39383953.Google Scholar
Franklin, ST, Young, JW and Nonnecke, BJ 1991. Effects of ketones, acetate, butyrate, and glucose on bovine lymphocyte proliferation. Journal of Dairy Science 74, 25072514.CrossRefGoogle ScholarPubMed
GfE (Society of Nutrition Physiolgy) 1991. Leitlinien für die Bestimmung der Verdaulichkeit von Rohnährstoffen an Wiederkäuern (Guidelines for determining the digestibility of crude ruminants). Journal of Animal Physiology and Animal Nutrition 65, 229234.Google Scholar
GfE (Society of Nutrition Physiolgy) 2001. Empfehlungen zur Energie- und Nährstoffversorgung der Milchkühe und Aufzuchtrinder (Recommendations of energy and nutrient supply for dairy cows and breeding cattle). DLG-Verlag, Frankfurt am Main, Germany.Google Scholar
Goff, JP 2006. Major advances in our understanding of nutritional influences on bovine health. Journal of Dairy Science 89, 12921301.CrossRefGoogle ScholarPubMed
Goyarts, T, Danicke, S, Grovel, N, Tiemann, U and Rothotter, HJ 2006. Methodical aspects of in vitro proliferation of porcine blood lymphocytes when exposed to deoxynivalenol (DON). Landbauforschung 56, 139148.Google Scholar
Grummer, RR 1995. Impact of changes in organic nutrient metabolism on feeding the transition dairy cow. Journal of Animal Science 73, 28202833.Google Scholar
Hayirli, A and Grummer, RR 2004. Factors affecting dry matter intake prepartum in relationship to etiology of peripartum lipid-related metabolic disorders: a review. Canadian Journal of Animal Science 84, 337347.Google Scholar
Hussen, J, Dänicke, S and Schuberth, HJ 2011. The effect of a long term dietary supplementation with conjugated linoleic acid (CLA) on the composition of bovine peripheral blood mononuclear cells (PBMC) and the concentration of IgG isotypes in blood and milk. Proceedings of the Society of Nutrition Physiology 20, 8585.Google Scholar
Kay, JK, Roche, JR, Moore, CE and Baumgard, LH 2006. Effects of dietary conjugated linoleic acid on production and metabolic parameters in transition dairy cows grazing fresh pasture. Journal of Dairy Research 73, 367377.Google Scholar
Kraft, W and Dürr, UM 2005. Klinische Labordiagnostik in der Tiermedizin (Clinical laboratory diagnostics in veterinary medicine). Schattauer Verlag, Stuttgart, Germany.Google Scholar
Kuhla, B, Albrecht, D, Kuhla, S and Metges, CC 2009. Proteome analysis of fatty liver in feed-deprived dairy cows reveals interaction of fuel sensing, calcium, fatty acid, and glycogen metabolism. Physiological Genomics 37, 8898.CrossRefGoogle ScholarPubMed
Lacetera, N, Scalia, D, Franci, O, Bernabucci, U, Ronchi, B and Nardone, A 2004. Short communication: effects of nonesterified fatty acids on lymphocyte function in dairy heifers. Journal of Dairy Science 87, 10121014.Google Scholar
Liermann, T 2008. Einfluss einer Zulage von pansengeschützter konjugierter Linolsäure(CLA) in Kombination mit Propylenglykol oder pansengeschütztem Fett auf Leistungsmerkmale, Stoffwechselparameter und den Energiestatus frischlaktierender Milchkühe (Effects of feeding rumen protected conjugated linoleic acids (CLA) alone or in combination with propylene glycol or rumen protected fat on performance and metabolic parameters and energy status of early lactation dairy cows). Dissertation, Technische Universität München, München, Germany, 188 pages.Google Scholar
Loiselle, MC, Ster, C, Talbot, BG, Zhao, X, Wagner, GF, Boisclair, YR and Lacasse, P 2009. Impact of postpartum milking frequency on the immune system and the blood metabolite concentration of dairy cows. Journal of Dairy Science 92, 19001912.Google Scholar
Loor, JJ, Everts, RE, Bionaz, M, Dann, HM, Morin, DE, Oliveira, R, Rodriguez-Zas, SL, Drackley, JK and Lewin, HA 2007. Nutrition-induced ketosis alters metabolic and signaling gene networks in liver of periparturient dairy cows. Physiological Genomics 32, 105116.Google Scholar
Mallard, BA, Dekkers, JC, Ireland, MJ, Leslie, KE, Sharif, S, Vankampen, CL, Wagter, L and Wilkie, BN 1998. Alteration in immune responsiveness during the peripartum period and its ramification on dairy cow and calf health. Journal of Dairy Science 81, 585595.Google Scholar
Moore, CE, Hafliger, HC, Mendivil, OB, Sanders, SR, Bauman, DE and Baumgard, LH 2004. Increasing amounts of conjugated linoleic acid progressively reduces milk fat synthesis immediately postpartum. Journal of Dairy Science 87, 18861895.Google Scholar
Nonnecke, BJ, Kimura, K, Goff, JP and Kehrli, ME 2003. Effects of the mammary gland on functional capacities of blood mononuclear leukocyte populations from periparturient cows. Journal of Dairy Science 86, 23592368.Google Scholar
Odens, LJ, Burgos, R, Innocenti, M, VanBaale, MJ and Baumgard, LH 2007. Effects of varying doses of supplemental conjugated linoleic acid on production and energetic variables during the transition period. Journal of Dairy Science 90, 293305.Google Scholar
Pappritz, J, Meyer, U, Kramer, R, Weber, EM, Jahreis, G, Rehage, J, Flachowsky, G and Dänicke, S 2011. Effects of long-term supplementation of dairy cow diets with rumen-protected conjugated linoleic acids (CLA) on performance, metabolic parameters and fatty acid profile in milk fat. Archives of Animal Nutrition 65, 89107.Google Scholar
Perfield, JW, Bernal-Santos, G, Overton, TR and Bauman, DE 2002. Effects of dietary supplementation of rumen-protected conjugated linoleic acid in dairy cows during established lactation. Journal of Dairy Science 85, 26092617.Google Scholar
Petzold, M, Meyer, U, Kersten, S, Spilke, J, Kramer, R, Jahreis, G and Dänicke, S 2013. Effects of conjugated linoleic acids and dietary concentrate proportion on performance, milk composition, milk yield and metabolic parameters of periparturient dairy cows. Archives of Animal Nutrition 67, 185201.Google Scholar
Renner, L, Schwabe, A, Doll, S, Holtershinken, M and Danicke, S 2011. Effect of rare earth elements on beef cattle growth performance, blood clinical chemical parameters and mitogen stimulated proliferation of bovine peripheral blood mononuclear cells in vitro and ex vivo. Toxicology Letters 201, 277284.Google Scholar
Renner, L, Pappritz, J, Kramer, R, Kersten, S, Jahreis, G and Dänicke, S 2012a. Fatty acid profile and proliferation of bovine blood mononuclear cells after conjugated linoleic acid supplementation. Lipids in Health and Disease 11, 17.Google Scholar
Renner, L, von Soosten, D, Sipka, A, Döll, S, Beineke, A, Schuberth, HJ and Dänicke, S 2012b. Effect of conjugated linoleic acid on proliferation and cytokine expression of bovine peripheral blood mononuclear cells and splenocytes ex vivo. Archives of Animal Nutrition 66, 7385.Google Scholar
Schulz, K, Frahm, J, Meyer, U, Kersten, S, Reiche, D, Rehage, J and Danicke, S 2014. Effects of prepartal body condition score and peripartal energy supply of dairy cows on postpartal lipolysis, energy balance and ketogenesis: an animal model to investigate subclinical ketosis. The Journal of Dairy Research 110.Google Scholar
Selberg, KT, Lowe, AC, Staples, CR, Luchini, ND and Badinga, L 2004. Production and metabolic responses of periparturient Holstein cows to dietary conjugated linoleic acid and trans-octadecenoic acids. Journal of Dairy Science 87, 158168.Google Scholar
Sigl, T, Schlamberger, G, Kienberger, H, Wiedemann, S, Meyer, HH and Kaske, M 2010. Rumen-protected conjugated linoleic acid supplementation to dairy cows in late pregnancy and early lactation: effects on milk composition, milk yield, blood metabolites and gene expression in liver. Acta veterinaria Scandinavia 52, 28.Google Scholar
Vangroenweghe, F, Lamote, I and Burvenich, C 2005. Physiology of the periparturient period and its relation to severity of clinical mastitis. Domestic Animal Endocrinology 29, 283293.CrossRefGoogle ScholarPubMed
von Soosten, D, Dänicke, S, Meyer, U, Weber, EM, Rehage, J and Flachowsky, G 2011. Effect of trans-10, cis-12 conjugated linoleic acid on performance, adipose depot weights, and liver weight in early-lactation dairy cows. Journal of Dairy Science 94, 28592870.Google Scholar