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Effects of sodium butyrate supplementation on reproductive performance and colostrum composition in gilts

Published online by Cambridge University Press:  04 April 2016

B. He
Affiliation:
Key Laboratory of Animal Physiology & Biochemistry, Ministry of Agriculture, Nanjing Agricultural University, Nanjing 210095, China
M. Wang
Affiliation:
Key Laboratory of Animal Physiology & Biochemistry, Ministry of Agriculture, Nanjing Agricultural University, Nanjing 210095, China
H. Guo
Affiliation:
Key Laboratory of Animal Physiology & Biochemistry, Ministry of Agriculture, Nanjing Agricultural University, Nanjing 210095, China
Y. Jia
Affiliation:
Key Laboratory of Animal Physiology & Biochemistry, Ministry of Agriculture, Nanjing Agricultural University, Nanjing 210095, China
X. Yang
Affiliation:
Key Laboratory of Animal Physiology & Biochemistry, Ministry of Agriculture, Nanjing Agricultural University, Nanjing 210095, China
R. Zhao*
Affiliation:
Key Laboratory of Animal Physiology & Biochemistry, Ministry of Agriculture, Nanjing Agricultural University, Nanjing 210095, China Jiangsu Collaborative Innovation Center of Meat Production and Processing, Quality and Safety Control, Nanjing 210095, China
*
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Abstract

Nutrients are essential for the health and survival of human beings and animals. Also, they play a major role in enhancing reproductive efficiency. The aim of the current study was to investigate the effects of sodium butyrate (SB) on reproductive performance and colostrum composition in gilts. A total of 40 Large White×Landrace replacement gilts (at the age of 160 to 175 days) were fed either a standard diet (control group, n=20) or standard diet top dressed with encapsulated SB at the level of 500 mg/kg (SB group, n=20) from 1 month before mating to 7 days after farrowing. The rate of gilts regular return to estrus after insemination was lower in SB group than the control group. The total number of piglets born (P=0.179) and the litter weight at birth (P=0.063) did not differ between the two treatment groups. However, the mean BW at day 7 tended to be greater in SB group (P=0.051) and average daily gain of piglets was greater (P=0.011) compared with control group. Colostrum samples were collected at parturition and the concentrations of total protein (P=0.197), cholesterol (P=0.161) and lactose (P=0.923) were not influenced by SB supplementation. However, compared with control gilts, colostrum from SB-treated gilts contained lower triglyceride (P=0.050). Moreover, colostrum concentrations of prolactin (P=0.005) and leptin (P=0.006) were significantly lower in SB group. No significant differences were noted for the colostral concentrations of cortisol (P=0.899), thyroxine (P=0.891) or triiodothyronine (P=0.194). The concentration of lipopolysaccharide in colostrum was not influenced by SB supplementation (P=0.972). However, colostrum from SB-treated gilts had significantly lower tumor necrosis factor α (TNFα) (P=0.030) and higher immunoglobulin A (IgA) (P=0.042). Collectively, SB supplementation could reduce the rate of gilts return to estrus, alter the composition of colostrum and enhance the growth rate of piglets. Moreover, SB could alter the immune function of newborn piglets through decreased production of TNFα and increased IgA concentration in colostrum.

Type
Research Article
Copyright
© The Animal Consortium 2016 

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References

Bourne, FJ and Curtis, J 1973. The transfer of immunoglobins IgG, IgA and IgM from serum to colostrum and milk in the sow. Immunology 24, 157162.Google ScholarPubMed
De Groot, N, Van Kuik-Romeijn, P, Lee, SH and De Boer, HA 2000. Increased immunoglobulin A levels in milk by over-expressing the murine polymeric immunoglobulin receptor gene in the mammary gland epithelial cells of transgenic mice. Immunology 101, 218224.Google ScholarPubMed
Decaluwé, R, Maes, D, Cools, A, Wuyts, B, De Smet, S, Marescau, B, De Deyn, PP and Janssens, GP 2014. Effect of peripartal feeding strategy on colostrum yield and composition in sows. Journal of Animal Science 92, 35573567.CrossRefGoogle ScholarPubMed
Devillers, N, Le Dividich, J and Prunier, A 2011. Influence of colostrum intake on piglet survival and immunity. Animal 5, 16051612.CrossRefGoogle ScholarPubMed
Endo, H, Niioka, M, Kobayashi, N, Tanaka, M and Watanabe, T 2013. Butyrate-producing probiotics reduce nonalcoholic fatty liver disease progression in rats: new insight into the probiotics for the gut-liver axis. PLoS One 8, e63388.CrossRefGoogle ScholarPubMed
Fang, CL, Sun, H, Wu, J, Niu, HH and Feng, J 2014. Effects of sodium butyrate on growth performance, haematological and immunological characteristics of weanling piglets. Journal of Animal Physiology and Animal Nutrition 98, 680685.CrossRefGoogle ScholarPubMed
Farmer, C, Robert, S and Rushen, J 1998. Bromocriptine given orally to periparturient of lactating sows inhibits milk production. Journal of Animal Science 76, 750757.Google ScholarPubMed
Farmer, C, Sorensen, MT, Robert, S and Petitclerc, D 1999. Administering exogenous porcine prolactin to lactating sows: milk yield, mammary gland composition, and endocrine and behavioral responses. Journal of Animal Science 77, 18511859.CrossRefGoogle ScholarPubMed
Fukae, J, Amasaki, Y, Yamashita, Y, Bohgaki, T, Yasuda, S, Jodo, S, Atsumi, T and Koike, T 2005. Butyrate suppresses tumor necrosis factor alpha production by regulating specific messenger RNA degradation mediated through a cis-acting AU-rich element. Arthritis and Rheumatism 52, 26972707.CrossRefGoogle ScholarPubMed
Guillemet, R, Hamard, A, Quesnel, H, Pere, MC, Etienne, M, Dourmad, JY and Meunier-Salaun, MC 2007. Dietary fibre for gestating sows: effects on parturition progress, behaviour, litter and sow performance. Animal 1, 872880.CrossRefGoogle ScholarPubMed
Huang, C, Song, P, Fan, P, Hou, C, Thacker, P and Ma, X 2015. Dietary sodium butyrate decreases postweaning diarrhea by modulating intestinal permeability and changing the bacterial communities in weaned piglets. Journal of Nutrition 145, 27742780.CrossRefGoogle Scholar
Le Dividich, J, Herpin, P, Paul, E and Strullu, F 1997. Effect of fat content of colostrum on voluntary colostrum intake and fat utilization in newborn pigs. Journal of Animal Science 75, 707713.CrossRefGoogle ScholarPubMed
Le Jan, C 1993. Secretory component and IgA expression by epithelial cells in sow mammary gland and mammary secretions. Research in Veterinary Science 55, 265270.CrossRefGoogle ScholarPubMed
Le Dividich, J, Rooke, JA and Herpin, P 2005. Review: Nutritional and immunological importance of colostrum for the new-born pig. Journal of Agricultural Science 143, 469485.Google Scholar
Lin, Y, Fang, ZF, Che, LQ, Xu, SY, Wu, D, Wu, CM and Wu, XQ 2014. Use of sodium butyrate as an alternative to dietary fiber: effects on the embryonic development and anti-oxidative capacity of rats. PLoS One 9, e97838.CrossRefGoogle ScholarPubMed
Liu, L, Liu, Y, Gao, F, Song, G, Wen, J, Guan, J, Yin, Y, Ma, X, Tang, B and Li, Z 2012a. Embryonic development and gene expression of porcine SCNT embryos treated with sodium butyrate. Journal of Experimental Zoology. Part B, Molecular and Developmental Evolution 318, 224234.CrossRefGoogle ScholarPubMed
Liu, L, Song, G, Gao, F, Guan, J, Tang, B and Li, Z 2012b. Transient exposure to sodium butyrate after germinal vesicle breakdown improves meiosis but not developmental competence in pig oocytes. Cell Biology International 36, 483490.CrossRefGoogle Scholar
Loisel, F, Farmer, C, Ramaekers, P and Quesnel, H 2013. Effects of high fiber intake during late pregnancy on sow physiology, colostrum production, and piglet performance. Journal of Animal Science 91, 52695279.CrossRefGoogle ScholarPubMed
Lu, H, Su, S and Ajuwon, KM 2012. Butyrate supplementation to gestating sows and piglets induces muscle and adipose tissue oxidative genes and improves growth performance. Journal of Animal Science 90 (suppl.), 430432.CrossRefGoogle ScholarPubMed
Lu, J, Zou, X and Wang, Y 2008. Effects of sodium butyrate on the growth performance, intestinal microflora and morphology of weanling pigs. Journal of Animal and Feed Sciences 17, 568578.CrossRefGoogle Scholar
Piva, A, Morlacchini, M, Casadei, G, Gatta, P, Biagi, G and Prandini, A 2009. Sodium butyrate improves growth performance of weaned piglets during the first period after weaning. Italian Journal of Animal Science 1, 3542.CrossRefGoogle Scholar
Quesnel, H, Meunier-Salaun, MC, Hamard, A, Guillemet, R, Etienne, M, Farmer, C, Dourmad, JY and Pere, MC 2009. Dietary fiber for pregnant sows: influence on sow physiology and performance during lactation. Journal of Animal Science 87, 532543.CrossRefGoogle ScholarPubMed
Salmon, H, Berri, M, Gerdts, V and Meurens, F 2009. Humoral and cellular factors of maternal immunity in swine. Developmental and Comparative Immunology 33, 384393.CrossRefGoogle ScholarPubMed
Serena, A, Jorgensen, H and Bach Knudsen, KE 2009. Absorption of carbohydrate-derived nutrients in sows as influenced by types and contents of dietary fiber. Journal of Animal Science 87, 136147.Google ScholarPubMed
Soliman, MM, Ahmed, MM, Salah-Eldin, AE and Abdel-Aal, AA 2011. Butyrate regulates leptin expression through different signaling pathways in adipocytes. Journal of Veterinary Science 12, 319323.CrossRefGoogle ScholarPubMed
Theil, PK, Nielsen, MO, Sørensen, MT and Lauridsen, C 2012. Nutritional physiology of pigs. In Lactation, milk and suckling with emphasis on Danish production conditions (ed. KE Bach Knudsen, NJ Kjeldsen, HD Poulsen and BB Jensen), pp. 147. Danish Pig Research Centre, Copenhagen, Denmark.Google Scholar
Wang, JF, Fu, SP, Li, SN, Hu, ZM, Xue, WJ, Li, ZQ, Huang, BX, Lv, QK, Liu, JX and Wang, W 2013. Short-chain fatty acids inhibit growth hormone and prolactin gene transcription via cAMP/PKA/CREB signaling pathway in dairy cow anterior pituitary cells. International Journal of Molecular Sciences 14, 2147421488.CrossRefGoogle ScholarPubMed
Weber, TE and Kerr, BJ 2008. Effect of sodium butyrate on growth performance and response to lipopolysaccharide in weanling pigs. Journal of Animal Science 86, 442450.CrossRefGoogle ScholarPubMed
Weber, TE, Ziemer, CJ and Kerr, BJ 2008. Effects of adding fibrous feedstuffs to the diet of young pigs on growth performance, intestinal cytokines, and circulating acute-phase proteins. Journal of Animal Science 86, 871881.CrossRefGoogle Scholar
Wolinski, J, Slupecka, M and Romanowicz, K 2014. Leptin and ghrelin levels in colostrum, milk and blood plasma of sows and pig neonates during the first week of lactation. Animal Science Journal 85, 143149.CrossRefGoogle ScholarPubMed
Woodside, B, Budin, R, Wellman, MK and Abizaid, A 2012. Many mouths to feed: the control of food intake during lactation. Frontiers in Neuroendocrinology 33, 301314.CrossRefGoogle ScholarPubMed
Zhang, Y, Proenca, R, Maffei, M, Barone, M, Leopold, L and Friedman, JM 1994. Positional cloning of the mouse obese gene and its human homologue. Nature 372, 425432.CrossRefGoogle ScholarPubMed