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Providing the plant extract silymarin to lactating sows: effects on litter performance and oxidative stress in sows

Published online by Cambridge University Press:  13 September 2016

C. Farmer*
Affiliation:
Agriculture and Agri-Food Canada, Sherbrooke R & D Centre, 2000 College St., Sherbrooke, QC, CanadaJ1M 0C8
J. Lapointe
Affiliation:
Agriculture and Agri-Food Canada, Sherbrooke R & D Centre, 2000 College St., Sherbrooke, QC, CanadaJ1M 0C8
I. Cormier
Affiliation:
La COOP Fédérée, Animal Nutrition Division, St-Romuald, QC, CanadaG6W 5M6
*
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Abstract

Silymarin is an extract from the plant milk thistle that was shown to have antioxidant and hyperprolactinemic properties. Taking into account the essential role of prolactin for lactating sows and the systemic oxidative stress occurring during lactation, it is of interest to investigate the potential beneficial effects of silymarin on lactating sows. A study was therefore carried out to determine the effects of providing either 1 or 8 g/day of the plant extract silymarin to lactating sows. Sows in first, second or third parity were fed conventional diets during gestation and, at farrowing, were assigned as controls (CTL, n=33), or were fed 1 g/day (SYL1, n=33) or 8 g/day (SYL8, n=33) of silymarin. The silymarin was provided in two equal amounts per day, and was fed throughout a 20-day lactation. The performance of sows and their litters was assessed and circulating concentrations of prolactin (days 7 and 18), urea (days 7 and 18) and oxidative status, via protein carbonyls and superoxide dismutase activity (day 18), were measured in sows. Milk samples were obtained on day 18 to measure standard composition. There was no effect of silymarin (P>0.10) on circulating prolactin or urea, or on oxidative damage to proteins or antioxidant potential in sows. Lactation feed intake, backfat and BW of sows were unaffected by treatment (P>0.10) as was the case for milk composition and piglet growth (P>0.10). Results demonstrate that providing up to 8 g/day of the plant extract silymarin to lactating sows had no beneficial effects in terms of circulating prolactin concentrations or oxidative status of sows, or in terms of performances of sows and their litters.

Type
Research Article
Copyright
© The Animal Consortium and Her Majesty the Queen in Right of Canada, as represented by the Minister of Agriculture and Agri-Food Canada 2016 

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References

Agriculture and Agri-Food Canada 1993. Recommended code of practice for the care and handling of farm animals – pigs. Publ. No. 1898E . Agriculture and Agri-Food Canada, Ottawa, ON, Canada.Google Scholar
Association Official Analytical Chemistry (AOAC) 2005. Official methods of analysis international, 18th edition. AOAC, Arlington, VA, USA.Google Scholar
Banaee, M, Sureda, A, Mirvaghefi, AR and Rafei, GR 2011. Effects of long-term silymarin oral supplementation on the blood biochemical profile of rainbow trout (Oncorhynchus mykiss). Fish Physiology and Biochemistry 37, 885896.Google Scholar
Berchieri-Ronchi, CB, Kim, SW, Zhao, Y, Correa, CR, Yeum, KJ and Ferreira, AL 2011. Oxidative stress status of highly prolific sows during gestation and lactation. Animal 5, 17741779.CrossRefGoogle ScholarPubMed
Cao, X, Fu, M, Wang, L, Liu, H, Deng, W, Qu, R, Su, W, Wei, Y, Xu, X and Yu, J 2012. Oral bioavailability of silymarin formulated as a novel 3-day delivery system based on porous silica nanoparticles. Acta Biomaterialia 8, 21042122.CrossRefGoogle ScholarPubMed
Capasso, R, Aviello, G, Capasso, F, Savino, F, Izzo, AA, Lembo, F and Borrelli, F 2009. Silymarin BIO-C®, an extract from Silybum marianum fruits, induces hyperprolactinemia in intact female rats. Phytomedicine 16, 839844.Google Scholar
Di Pierro, F, Callegari, A, Carotenuto, D and Tapia, MM 2008. Clinical efficacy, safety and tolerability of BIO-C® (micronized Silymarin) as a galactagogue. Acta Biomedica 79, 205210.Google Scholar
Dixit, N, Baboota, S, Kohli, K, Ahmad, S and Ali, J 2007. Silymarin: a review of pharmacological aspects and bioavailability enhancement approaches. Indian Journal of Pharmacology 39, 172179.Google Scholar
Farmer, C 2001. The role of prolactin for mammogenesis and galactopoiesis in swine. Livestock Production Science 70, 105113.CrossRefGoogle Scholar
Farmer, C, Lapointe, J and Palin, MF 2014. Effects of the plant extract silymarin on prolactin concentrations, mammary gland development, and oxidative stress in gestating gilts. Journal of Animal Science 92, 29222930.Google Scholar
Farmer, C, Robert, S and Rushen, J 1998. Bromocriptine given orally to periparturient or lactating sows inhibits milk production. Journal of Animal Science 76, 750757.Google Scholar
Feng, B, Meng, R, Huang, B, Shen, S, Bi, Y and Zhu, D 2016. Silymarin alleviates hepatic oxidative stress and protects against metabolic disorders in high-fat diet-fed mice. Free Radical Research 50, 314327.Google Scholar
Gabrielova, E, Kren, V, Jaburek, M and Modriansky, M 2015. Silymarin component 2,3-dehydrosilybin attenuates cardiomyocyte damage following hypoxia/reoxygenation by limiting oxidative stress. Physiological Research 64, 7991.CrossRefGoogle ScholarPubMed
Garavaglia, L, Galletti, S and Tedesco, D 2015. Silymarin and lycopene administration in periparturient dairy cows: effects on milk production and oxidative status. New Zealand Veterinary Journal 63, 313318.Google Scholar
Gharagozloo, M, Velardi, E, Bruscoli, S, Agostini, M, Di Sante, M, Donato, V, Amirghofran, Z and Riccardi, C 2010. Silymarin suppress CD4+ T cell activation and proliferation: effects on NF-kappaB activity and IL-2 production. Pharmacological Research 61, 405409.Google Scholar
Giese, LA 2001. Milk thistle and the treatment of hepatitis. Gastroenterology Nursing 24, 9597.Google Scholar
Gupta, OP, Sing, S, Bani, S, Sharma, N, Malhotra, S, Gupta, BD, Banerjee, SK and Handa, SS 2000. Anti-inflammatory and anti-arthritic activities of silymarin acting through inhibition of 5-lipoxygenase. Phytomedicine 7, 2124.Google Scholar
Hoving, LL, Soede, NM, Feitsma, H and Kemp, B 2012. Lactation weight loss in primiparous sows: consequences for embryo survival and progesterone and relations with metabolic profiles. Reproduction in Domestic Animals 47, 10091016.CrossRefGoogle ScholarPubMed
Huntington, GB 1984. Net absorption of glucose and nitrogenous compounds by lactating Holstein cows. Journal of Dairy Science 67, 19191927.Google Scholar
Kiruthiga, PV, Shafreen, RB, Pandian, SK and Devi, KP 2007. Silymarin protection against major reactive oxygen species released by environmental toxins: exogenous H2O2 exposure in erythrocytes. Basic and Clinical Pharmacology and Toxicology 100, 414419.Google Scholar
Kowaltowski, AJ, de Souza-Pinto, NC, Castilho, RF and Vercesi, AE 2009. Mitochondria and reactive oxygen species. Free Radical Biology and Medicine 47, 333343.Google Scholar
Lapointe, J 2014. Mitochondria as promising targets for nutritional interventions aiming to improve performance and longevity of sows. Journal of Animal Physiology and Animal Nutrition 98, 809821.Google Scholar
Lapointe, J, Stepanyan, Z, Bigras, E and Hekimi, S 2009. Reversal of the mitochondrial phenotype and slow development of oxidative biomarkers of aging in long-lived Mclk1+/− mice. Journal of Biological Chemistry 284, 2036420374.Google Scholar
Loisel, F, Farmer, C, Ramaekers, P and Quesnel, H 2014. Colostrum yield and piglet growth during lactation are related to gilt metabolic and hepatic status prepartum. Journal of Animal Science 92, 29312941.Google Scholar
Loisel, F, Quesnel, H and Farmer, C 2013. Short communication: effect of silymarin (Silybum marianum) treatment on prolactin concentrations in cyclic sows. Canadian Journal of Animal Science 93, 227230.CrossRefGoogle Scholar
Miller, YJ, Collins, AM, Smits, RJ, Thompson, PC and Holyoake, PK 2012. Providing supplemental milk to piglets preweaning improves the growth but not survival of gilt progeny compared with sow progeny. Journal of Animal Science 90, 50785085.Google Scholar
Neretti, N, Wang, PY, Brodsky, AS, Nyguyen, HH, White, KP, Rogina, B and Helfand, SL 2009. Long-lived Indy induces reduced mitochondrial reactive oxygen species production and oxidative damage. Proceedings of the National Academy of Sciences of the United States of America 106, 22772282.Google Scholar
Powe, CE, Puopolo, KM, Newburg, DS, Lönnerdal, B, Chen, C, Allen, M, Merewood, A, Worden, S and Welt, CK 2011. Effects of recombinant human prolactin on breast milk composition. Pediatrics 127, 359366.CrossRefGoogle ScholarPubMed
Robert, S, de Passillé, AMB, St-Pierre, N, Dubreuil, P, Pelletier, G, Petitclerc, D and Brazeau, P 1989. Effect of the stress of injection on the serum concentrations of cortisol, prolactin, and growth hormone in gilts and lactating sows. Canadian Journal of Animal Science 69, 663672.Google Scholar
Smith, BB and Wagner, WC 1985. Effect of dopamine agonists or antagonists, TRH, stress and piglet removal on plasma prolactin concentrations in lactating gilts. Theriogenology 23, 283296.CrossRefGoogle ScholarPubMed
Starvaggi Cucuzza, L, Motta, M, Miretti, S, Macchi, E, Martignani, E, Accornero, P and Baratta, M 2010. Positive effect of silymarin on cell growth and differentiation in bovine and murine mammary cells. Journal of Animal Physiology and Animal Nutrition 94, 111117.Google Scholar
Surai, PF 2015. Silymarin as a natural antioxidant: an overview of the current evidence and perspectives. Antioxidants 4, 204247.Google Scholar
Tedesco, D, Tava, A, Galletti, S, Tameni, M, Varisco, G, Costa, A and Steidler, S 2004. Effects of silymarin, a natural hepatoprotector, in periparturient dairy cows. Journal of Dairy Science 87, 22392247.CrossRefGoogle ScholarPubMed
Turgut, F, Bayrak, O, Catal, F, Bayrak, R, Atmaca, AF, Koc, A, Akbas, A, Akcay, A and Unal, D 2008. Antioxidant and protective effects of silymarin on ischemia and reperfusion injury in the kidney tissues of rats. International Urology and Nephrology 40, 453460.Google Scholar
Wu, CH, Huang, SM and Yen, GC 2011. Silymarin: a novel antioxidant with antiglycation and antiinflammatory properties in vitro and in vivo . Antioxidants and Redox Signaling 14, 353366.CrossRefGoogle ScholarPubMed
Yi, D, Gu, L, Ding, B, Li, M, Hou, Y, Wang, L and Gong, J 2012. Effects of dietary silymarin supplementation on growth performance and oxidative status in Carassius auratus gibelio . Journal of Animal Veterinary Advances 11, 33993404.Google Scholar
Zhao, F, Shi, D, Li, T, Li, L and Zhao, M 2015. Silymarin attenuates paraquat-induced lung injury via Nrf2-mediated pathway in vivo and in vitro . Clinical and Experimental Pharmacology and Physiology 42, 988998.CrossRefGoogle ScholarPubMed