Kosina, P.; Gregorova, J.; Gruz, J.; Vacek, J.; Kolar, M.; Vogel, M.; Roos, W.; Naumann, K.; Simanek, V.; Ulrichova, J. Phytochemical and antimicrobial characterization of Macleaya cordata herb. Fitoterapia 2010, 81, 1006–1012, doi:10.1016/j.fitote.2010.06.020.
Wu, Y.; Zhao, N.J.; Cao, Y.; Sun, Z.; Wang, Q.; Liu, Z.Y.; Sun, Z.L. Sanguinarine metabolism and pharmacokinetics study in vitro and in vivo. J. Vet. Pharmacol. Ther. 2020, 43, 208–214, doi:10.1111/jvp.12835.
Zhao, L.; Matulka, R.A.; von Alvensleben, S.; Morlacchini, M. Residue Study for a Standardized Macleaya cordata Extract in Growing‐Finishing Swine. Open J. Anim. Sci. 2017, 7, 93–104, doi:10.4236/ojas.2017.72008.
Newton, S.M.; Lau, C.; Gurcha, S.S.; Besra, G.S.; Wright, C.W. The evaluation of forty‐three plant species for in vitro antimycobacterial activities; isolation of active constituents from Psoralea corylifolia and Sanguinaria canadensis. J. Ethnopharmacol. 2002, 79, 57–67, doi:10.1016/S0378‐8741(01)00350‐6.
Tanaka, T.; Metori, K.; Mineo, S.; Hirotani, M.; Furuya, T.; Kobayashi, S. Inhibitory Effects of Berberine‐Type Alkaloids on Elastase. Planta Med. 1993, 59, 200–202, doi:10.1055/s‐2006‐959651.
Niu, X.; Fan, T.; Li, W.; Xing, W.; Huang, H. The anti‐inflammatory effects of sanguinarine and its modulation of inflammatory mediators from peritoneal macrophages. Eur. J. Pharmacol. 2012, 689, 262–269, doi:10.1016/j.ejphar.2012.05.039.
Chen, J.; Kang, B.; Yao, K.; Fu, C.; Zhao, Y. Effects of dietary Macleaya cordata extract on growth performance, immune responses, antioxidant capacity, and intestinal development in weaned piglets. J. Appl. Anim. Res. 2019, 47, 349–356, doi:10.1080/09712119.2019.1636800.
Chaturvedi, M.M.; Kumar, A.; Darnay, B.G.; Chainy, G.B.N.; Agarwal, S.; Aggarwal, B.B. Sanguinarine (Pseudochelerythrine) Is a Potent Inhibitor of NF‐κB Activation, IκBα Phosphorylation, and Degradation. J. Biol. Chem. 1997, 272, 30129–30134, doi:10.1074/jbc.272.48.30129.
Khadem, A.; Soler, L.; Everaert, N.; Niewold, T.A. Growth promotion in broilers by both oxytetracycline and Macleaya cordata extract is based on their anti‐inflammatory properties. Br. J. Nutr. 2014, 112, 1110–1118, doi:10.1017/S0007114514001871.
Kikusato, M.; Xue, G.; Pastor, A.; Niewold, T.A.; Toyomizu, M. Effects of plant‐derived isoquinoline alkaloids on growth performance and intestinal function of broiler chickens under heat stress. Poult. Sci. 2021, 100, 957–963, doi:10.1016/j.psj.2020.11.050.
Kantas, D.; Papatsiros, V.G.; Tassis, P.D.; Athanasiou, L.V.; Tzika, E.D. The effect of a natural feed additive (Macleaya cordata), containing sanguinarine, on the performance and health status of weaning pigs. Anim. Sci. J. 2015, 86, 92–98, doi:10.1111/asj.12240.
Goodarzi Boroojeni, F.; Männer, K.; Zentek, J. The impacts of Macleaya cordata extract and naringin inclusion in post‐weaning piglet diets on performance, nutrient digestibility and intestinal histomorphology. Arch. Anim. Nutr. 2018, 72, 178–189, doi:10.1080/1745039X.2018.1459342.
Tantasuparuk, W.; Dalin, A.‐M.; Lundeheim, N.; Kunavongkrit, A.; Einarsson, S. Body weight loss during lactation and its influence on weaning‐to‐service interval and ovulation rate in Landrace and Yorkshire sows in the tropical environment of Thailand. Anim. Reprod. Sci. 2001, 65, 273–281, doi:10.1016/S0378‐4320(00)00218‐9.
Eissen, J.J.; Apeldoorn, E.J.; Kanis, E.; Verstegen, M.W.A.; de Greef, K.H. The importance of a high feed intake during lactation of primiparous sows nursing large litters. J. Anim. Sci. 2003, 81, 594–603, doi:10.2527/2003.813594x.
Leonard, S.G.; Sweeney, T.; Bahar, B.; Lynch, B.P.; O’Doherty, J. V Effect of maternal fish oil and seaweed extract supplementation on colostrum and milk composition, humoral immune response, and performance of suckled piglets1. J. Anim. Sci. 2010, 88, 2988–2997, doi:10.2527/jas.2009‐2764.
Farmer, C.; Quesnel, H. Nutritional, hormonal, and environmental effects on colostrum in sows. J. Anim. Sci. 2009, 87, 56–64, doi:10.2527/jas.2008‐1203.
Leblois, J.; Massart, S.; Soyeurt, H.; Grelet, C.; Dehareng, F.; Schroyen, M.; Li, B.; Wavreille, J.; Bindelle, J.; Everaert, N. Feeding sows resistant starch during gestation and lactation impacts their faecal microbiota and milk composition but shows limited effects on their progeny. PLoS ONE 2018, 13, e0199568, doi:10.1371/journal.pone.0199568.
Leblois, J.; Massart, S.; Li, B.; Wavreille, J.; Bindelle, J.; Everaert, N. Modulation of piglets’ microbiota: Differential effects by a high wheat bran maternal diet during gestation and lactation. Sci. Rep. 2017, 7, doi:10.1038/s41598‐017‐07228‐2.
Chatelais, L.; Jamin, A.; Le Guen, C.G.; Lallès, J.P.; Le Huërou‐Luron, I.; Boudry, G. The level of protein in milk formula modifies ileal sensitivity to LPS later in life in a piglet model. PLoS ONE 2011, 6, doi:10.1371/journal.pone.0019594.
Meissonnier, G.M.; Pinton, P.; Laffitte, J.; Cossalter, A.M.; Gong, Y.Y.; Wild, C.P.; Bertin, G.; Galtier, P.; Oswald, I.P. Immunotoxicity of aflatoxin B1: Impairment of the cell‐mediated response to vaccine antigen and modulation of cytokine expression. Toxicol. Appl. Pharmacol. 2008, 231, 142–149, doi:10.1016/j.taap.2008.04.004.
Gourbeyre, P.; Berri, M.; Lippi, Y.; Meurens, F.; Vincent‐Naulleau, S.; Laffitte, J.; Rogel‐Gaillard, C.; Pinton, P.; Oswald, I.P. Pattern recognition receptors in the gut: Analysis of their expression along the intestinal tract and the crypt/villus axis. Physiol. Rep. 2015, 3, e12225, doi:10.14814/phy2.12225.
Kim, S.W.; Mateo, R.D.; Yin, Y.L.; Wu, G. Functional amino acids and fatty acids for enhancing production performance of sows and piglets. Asian‐Australas. J. Anim. Sci. 2007, 20, 295–306, doi:10.5713/ajas.2007.295.
Kemp, B.; Soede, N. Reproductive problems in primiparous sows. Proc. 18th IPVS Congr. 2004, 2, 843–848. .
Baidoo, S.K.; Aherne, F.X.; Kirkwood, R.N.; Foxcroft, G.R. Effect of feed intake during lactation and after weaning on sow reproductive performance. Can. J. Anim. Sci. 1992, 72, 911–917, doi:10.4141/cjas92‐103.
Zak, L.J.; Cosgrove, J.R.; Aherne, F.X.; Foxcroft, G.R. Pattern of Feed Intake and Associated Metabolic and Endocrine Changes Differentially Affect Postweaning Fertility in Primiparous Lactating Sows. J. Anim. Sci. 1997, 75, 208–216, doi:10.2527/1997.751208x.
Kirkwood, R.N.; Baidoo, S.K.; Aherne, F.X.; Sather, A.P. The Influence of feeding level during lactation on the occurrence and endocrinology of the postweaning estrus in sows. Can. J. Anim. Sci. 1987, 67, 405–415, doi:10.4141/cjas87‐039.
Mullan, B.P.; Williams, I.H. The chemical composition of sows during their first lactation. Anim. Sci. 1990, 51, 375–387, doi:10.1017/S0003356100005523.
Charette, R.; Bigras‐Poulin, M.; Martineau, G.‐P. Body condition evaluation in sows. Livest. Prod. Sci. 1996, 46, 107–115, doi:10.1016/0301‐6226(96)00022‐X.
Kim, J.S.; Yang, X.; Pangeni, D.; Baidoo, S.K. Relationship between backfat thickness of sows during late gestation and reproductive efficiency at different parities. Acta Agric. Scand. A Anim. Sci. 2015, 65, 1–8, doi:10.1080/09064702.2015.1045932.
De Rensis, F.; Gherpelli, M.; Superchi, P.; Kirkwood, R.N. Relationships between backfat depth and plasma leptin during lactation and sow reproductive performance after weaning. Anim. Reprod. Sci. 2005, 90, 95–100, doi:10.1016/j.anireprosci.2005.01.017.
Serenius, T.; Stalder, K.J.; Baas, T.J.; Mabry, J.W.; Goodwin, R.N.; Johnson, R.K.; Robison, O.W.; Tokach, M.; Miller, R.K. National Pork Producers Council Maternal Line National Genetic Evaluation Program: A comparison of sow longevity and trait associations with sow longevity. J. Anim. Sci. 2006, 84, 2590–2595, doi:10.2527/jas.2005‐499.
McMorris, T.; Swain, J.; Smith, M.; Corbett, J.; Delves, S.; Sale, C.; Harris, R.C.; Potter, J. Heat stress, plasma concentrations of adrenaline, noradrenaline, 5‐hydroxytryptamine and cortisol, mood state and cognitive performance. Int. J. Psychophysiol. 2006, 61, 204–215, doi:10.1016/j.ijpsycho.2005.10.002.
Becker, B.A.; Nienaber, J.A.; Christenson, R.K.; Manak, R.C.; DeShazer, J.A.; Hahn, G.L. Peripheral concentrations of cortisol as an indicator of stress in the pig. Am. J. Vet. Res. 1985, 46, 1034–1038.
Theil, P.K.; Nielsen, M.O.; Sørensen, M.T.; Lauridsen, C. Chapter 17—Lactation, milk and suckling. Nutr. Physiol. Pigs 2012, 1– 49. Available online: http://vsp.lf.dk/~/media/Files/Laerebog_fysiologi/Chapter 17.ashx (accessed on 22 July 2021).
Spincer, J.; Rook, J.A.F.; Towers, K.G. The uptake of plasma constituents by the mammary gland of the sows. Biochem. J. 1969, 111, 727–732, doi:10.1042/bj1110727.
Salehi, B.; Ata, A.; Kumar, N.V.A.; Sharopov, F.; Ramírez‐Alarcón, K.; Ruiz‐Ortega, A.; Ayatollahi, S.A.; Fokou, P.V.T.; Kobarfard, F.; Zakaria, Z.A.; et al. Antidiabetic Potential of Medicinal Plants and Their Active Components. Biomolecules. 2019, 9, 551, doi:10.3390/biom9100551.
Pan, G.Y.; Huang, Z.J.; Wang, G.J.; Fawcett, J.P.; Liu, X.D.; Zhao, X.C.; Sun, J.G.; Xie, Y.Y. The antihyperglycaemic activity of berberine arises from a decrease of glucose absorption. Planta Med. 2003, 69, 632–636, doi:10.1055/s‐2003‐41121.
Père, M.C.; Etienne, M.; Dourmad, J.Y. Adaptations of glucose metabolism in multiparous sows: Effects of pregnancy and feeding level. J. Anim. Sci. 2000, 78, 2933–2941, doi:10.2527/2000.78112933x.
Zou, C.S.; Wang, Y.J.; Zou, H.; Ding, N.; Geng, N.N.; Cao, C.W.; Zhang, G.C. Sanguinarine in Chelidonium majus induced antifeeding and larval lethality by suppressing food intake and digestive enzymes in Lymantria dispar. Pestic. Biochem. Physiol. 2019, 153, 9–16.
Markowska‐Daniel, I.; Pomorska‐Mól, M.; Pejsak, Z. Dynamic changes of immunoglobulin concentrations in pig colostrum and serum around parturition. Pol. J. Vet. Sci. 2010, 13, 21–27.
Dividich, J.L.; Rooke, J.A.; Herpin, P. Nutritional and immunological importance of colostrum for the new‐born pig. J. Agric. Sci. 2005, 143, 469–485.
Farmer, C.; Devillers, N.; Rooke, J.A.; Le Dividich, J. Colostrum production in swine: From the mammary glands to the piglets. Pigs News Inf. 2006, 27, doi:10.1079/PAVSNNR20061003.
Burrin, D.G.; Shulman, R.J.; Reeds, P.J.; Davis, T.A.; Gravitt, K.R. Porcine colostrum and milk stimulate visceral organ and skeletal muscle protein synthesis in neonatal piglets. J. Nutr. 1992, 122, 1205–1213, doi:10.1093/jn/122.6.1205.
Kuralkar, P.; Kuralkar, S.V. Nutritional and immunological importance of colostrum for the new born. Vet. World 2010, 3, 46– 47.
Everaert, N.; Van Cruchten, S.; Weström, B.; Bailey, M.; Van Ginneken, C.; Thymann, T.; Pieper, R. A review on early gut maturation and colonization in pigs, including biological and dietary factors affecting gut homeostasis. Anim. Feed Sci. Technol. 2017, 233, 89–103, doi:10.1016/j.anifeedsci.2017.06.011.
Silva, B.A.N.; Noblet, J.; Oliveira, R.F.M.; Donzele, J.L.; Primot, Y.; Renaudeau, D. Effects of dietary protein concentration and amino acid supplementation on the feeding behavior of multiparous lactating sows in a tropical humid climate. J. Anim. Sci. 2009, 87, 2104–2112, doi:10.2527/jas.2008‐1332.