2. Wang HY, Chen S, Xue RY, et al. Arsenic ingested early in life is more readily absorbed: mechanistic insights from gut microbiota, gut metabolites, and intestinal morphology and functions. Environ Sci Technol 2023;57:1017–27.
https://doi.org/10.1021/acs.est.2c04584
3. De Gregorio V, Imparato G, Urciuolo F, Netti PA. Micro-patterned endogenous stroma equivalent induces polarized crypt-villus architecture of human small intestinal epithelium. Acta Biomater 2018;81:43–59.
https://doi.org/10.1016/j.actbio.2018.09.061
5. Freddo AM, Shoffner SK, Shao Y, et al. Coordination of signaling and tissue mechanics during morphogenesis of murine intestinal villi: a role for mitotic cell rounding. Integr Biol 2016;8:918–28.
https://doi.org/10.1039/c6ib00046k
6. Kondrashina A, Arranz E, Cilla A, et al. Coupling in vitro food digestion with in vitro epithelial absorption; recommendations for biocompatibility. Crit Rev Food Sci Nutr 2024;64:9618–36.
https://doi.org/10.1080/10408398.2023.2214628
7. Anthony A, Dhillon AP, Thrasivoulou C, Pounder RE, Wakefield AJ. Pre-ulcerative villous contraction and microvascular induced by indomethacin in the rat jejunum: a detailed morphological study. Aliment Pharmacol Ther 1995;9:605–13.
https://doi.org/10.1111/j.1365-2036.1995.tb00429.x
12. Santos A, Valdés C, Giráldez FJ, et al. Feed efficiency and the liver proteome of fattening lambs are modified by feed restriction during the suckling period. Animal 2018;12:1838–46.
https://doi.org/10.1017/S1751731118000046
13. Zhao X, Fu HY, Qiu SN, et al. Effects of early protein restriction on the growth performance and gut development of pigs fed diets with or without antibiotic. Animal 2020;14:1392–401.
https://doi.org/10.1017S1751731119002921
14. Amoah K, Dong X, Tan B, et al. Effects of three probiotic strains (Bacillus coagulans, B. licheniformis and Paenibacillus polymyxa) on growth, immune response, gut morphology and microbiota, and resistance against Vibrio harveyi of northern whitings, Sillago sihama Forsskál (1775). Anim Feed Sci Technol 2021;277:114958.
https://doi.org/10.1016/j.anifeedsci.2021.114958
15. Ayman U, Akter L, Islam R, et al. Dietary chitosan oligosaccharides improves health status in broilers for safe poultry meat production. Ann Agric Sci 2022;67:90–8.
https://doi.org/10.1016/j.aoas.2022.05.003
18. Xiao X, Liang JR, Yang HM, Wan XL, Wang ZY. Vitamin A deficiency or critical excess has negative effects on the growth performance, slaughter performance, and meat quality of goslings. Anim Feed Sci Technol 2021;280:115064.
https://doi.org/10.1016/j.anifeedsci.2021.115064
20. Wu LX, Li QL, Luo Z, et al. Effects of dietary vitamin D3 and carbohydrate levels on growth performance, carbohydrate metabolism, and intestinal health of yellow catfish (Pelteobagrus fulvidraco). Aquaculture 2024;592:741136.
https://doi.org/10.1016/j.aquaculture.2024.741136
21. Incharoen T, Yamauchi K, Erikawa T, Gotoh H. Histology of intestinal villi and epithelial cells in chickens fed low-crude protein or low-crude fat diets. Ital J Anim Sci 2010;9:e82.
https://doi.org/10.4081/ijas.2010.e82
22. Santos MJB, Ludke MCMM, Silva LM, et al. Complexed amino acid minerals vs. bis-glycinate chelated minerals: impact on the performance of old laying hens. Anim Nutr 2024;16:395–408.
https://doi.org/10.1016/j.aninu.2023.11.006
23. Rostamkhani AR, Shahir MH, Lemme A, Anarkooli IJ, Abdi Z. Impact of early feeding of highly available carbohydrate source on subsequent growth performance, carcass traits, blood biochemical parameters, and intestinal morphology of broilers. J Appl Poult Res 2024;33:100399.
https://doi.org/10.1016/j.japr.2023.100399
25. Cao M, Che L, Wang J, et al. Effects of maternal over- and undernutrition on intestinal morphology, enzyme activity, and gene expression of nutrient transporters in newborn and weaned pigs. Nutrition 2014;30:1442–7.
https://doi.org/10.1016/j.nut.2014.04.016
27. Berrocoso JD, Kida R, Singh AK, Kim YS, Jha R. Effect of in ovo injection of raffinose on growth performance and gut health parameters of broiler chicken. Poult Sci 2017;96:1573–80.
https://doi.org/10.3382/ps/pew430
29. Song J, Li Q, Li P, et al. The effects of inulin on the mucosal morphology and immune status of specific pathogen-free chickens. Poult Sci 2018;97:3938–46.
https://doi.org/10.3382/ps/pey260
30. Liao L, Li J, Li J, Huang Y, Wu Y. Effects of Astragalus polysaccharides on intestinal morphology and intestinal immune cells of Muscovy ducklings infected with Muscovy duck reovirus. Poult Sci 2021;100:64–72.
https://doi.org/10.1016/j.psj.2020.10.021
31. Feng Y, Wu Y, Wang J, et al. Enteromorpha prolifera polysaccharide-Fe (III) complex promotes intestinal development as a new iron supplement. Sci China Life Sci 2025;68:219–31.
https://doi.org/10.1007/s11427-023-2562-9
32. Guo G, Chen J, Peng S, et al. Effects of fucoidan on small intestinal tissue morphology, digestive enzyme activity and antioxidant indices of weaned lambs. Chin J Anim Nutr 2022;34:5206–18.
https://10.3969/j.issn.1006-267x.2022.08.043
35. Wang X, Wang W, Wang L, et al. Lentinan modulates intestinal microbiota and enhances barrier integrity in a piglet model challenged with lipopolysaccharide. Food Funct 2019;10:479–89.
https://doi.org/10.1039/C8Fo02438C
36. Wang Y, Chen B, Cao J, et al. Effects of mulberry leaf flavonoids on intestinal mucosal morphology and intestinal flora of Litopenaeus vannamei. Chin J Anim Nutr 2020;32:1817–25.
38. Liu A, Gong Z, Lin L, et al. Effects of l-theanine on glutamine metabolism in enterotoxigenic Escherichia coli (E44813)-stressed and non-stressed rats. J Funct Foods 2020;64:103670.
https://doi.org/10.1016/j.jff.2019.103670
39. Hu F, Liu Y, Liang X, Yang H, Xu H, Han F. To investigate the effect of oregano oil on ulcerative colitis mice based on intestinal flora and inflammatory factors. Chin Tradit Pat Med 2023;4:1294–300.
42. Liu Y, Song M, Che TM, et al. Dietary plant extracts alleviate diarrhea and alter immune responses of weaned pigs experimentally infected with a pathogenic Escherichia coli. J Anim Sci 2013;91:5294–306.
https://doi.org/10.2527/jas.2012-6194
43. Song Z, Zhao GY, Dong Y, et al. Effect of compound plant essential oils on structure of intestinal mucosa and antioxidant capacity of weaned piglets challenged with lipopolysaccharide. China Anim Husb Vet Med 2019;46:684–9.
https://doi.org/10.16431/j.cnki.1671-7236.2019.03.006
44. Wang J, Yang X, Qi Q, et al. Effects of curcumin on growth performance, meat quality and intestinal health of Cherry Valley ducks. Anim Husb Vet Med 2023;55:29–37.
47. Wang L, Song S, Cao Y, et al. Effects of Gelsemium elegans alkaloids on growth performance in weaned piglets. Chin J Vet Med 2023;59:136–43.
48. Chen J, Kang B, Zeng J, et al. Effects of dietary sanguinarine on growth performance, intestinal mucosal morphology and immune function of small intestinal mucosa of weaned piglets. Chin J Anim Nutr 2018;30:1845–53.
51. Hao T, Zhang L, Li B, et al. Effects of saccharicterpenin-supplemented diets on body composition, activity of intestinal enzymes, blood lipid and intestinal histology of juvenile turbot (Scophthalmus maximus). J Shanghai Ocean Univ 2015;24:391–402.
52. Huang P, Zhao SS, Zhang XW, Zhang TT, Xiao CB. Effects of dietary saccharicterpenin on mucosal structure of small intestine in Gushi chickens. Chin J Anim Nutr 2011;23:2016–23.
https://10.3969/j.issn.1006-267x.2011.11.024
54. Zheng WC, Xu J, Yang L. Effects of probiotics and organic acids on growth performance, intestinal morphology and immune indexes of weaned piglets. Guangdong Feed 2016;25:25–8.
55. Xu YJ, Ning SQ, Su SL, et al. The fundamental role of dietary amino acids in maintaining or improving intestinal health in weaned piglets. Swine Ind Sci 2022;39:80–4.
57. Awad WA, Ghareeb K, Abdel-Raheem S, Böhm J. Effects of dietary inclusion of probiotic and synbiotic on growth performance, organ weights, and intestinal histomorphology of broiler chickens. Poult Sci 2009;88:49–56.
https://doi.org/10.3382/ps.2008-00244
58. Tůmová E, Volek Z, Chodová D, et al. The effect of 1-week feed restriction on performance, digestibility of nutrients and digestive system development in the growing rabbit. Animal 2016;10:1–9.
https://doi.org/10.1017/S1751731115001810
60. Guo YJ, Wang ZY, Wang YS, et al. Impact of drinking water supplemented 2-hydroxy-4-methylthiobutyric acid in combination with acidifier on performance, intestinal development, and microflora in broilers. Poult Sci 2022;101:101661.
https://doi.org/10.1016/j.psj.2021.101661
61. Elhassan MMO, Ali AM, Blanch A, Kehlet AB, Madekurozwa MC. Morphological responses of the small intestine of broiler chicks to dietary supplementation with a probiotic, acidifiers, and their combination. J Appl Poult Res 2019;28:108–17.
https://doi.org/10.3382/japr/pfy042
62. Tiwari UP, Chen H, Kim SW, Jha R. Supplemental effect of xylanase and mannanase on nutrient digestibility and gut health of nursery pigs studied using both in vivo and in vitro models. Anim Feed Sci Technol 2018;245:77–90.
https://doi.org/10.1016/j.anifeedsci.2018.07.002
63. Pekel AY, Horn NL, Adeola O. The efficacy of dietary xylanase and phytase in broiler chickens fed expeller-extracted camelina meal. Poult Sci 2017;96:98–107.
https://doi.org/10.3382/ps/pew183
65. Li H, Ran T, He Z, Yan Q, Tang S, Tan Z. Postnatal developmental changes of the small intestinal villus height, crypt depth and hexose transporter mRNA expression in supplemental feeding and grazing goats. Small Rumin Res 2016;141:106–12.
https://doi.org/10.1016/j.smallrumres.2016.07.012
66. Wang JX, Li P, Zhang XT, Ye LX. Developmental morphology study on the stomach of African ostrich chicks. Poult Sci 2017;96:2006–12.
https://doi.org/10.3382/ps/pew504
67. Schaefer CM, Corsiglia CM, Mireles A Jr, Koutsos EA. Turkey breeder hen age affects growth and systemic and intestinal inflammatory responses in female poults examined at different ages posthatch. Poult Sci 2006;85:1755–63.
https://doi.org/10.1093/ps/85.10.1755
68. Refaey MM, Li D, Tian X, et al. High stocking density alters growth performance, blood biochemistry, intestinal histology, and muscle quality of channel catfish Ictalurus punctatus. Aquaculture 2018;492:73–81.
https://doi.org/10.1016/j.aquaculture.2018.04.003
69. Applegate TJ, Karcher DM, Lilburn MS. Comparative development of the small intestine in the turkey poult and Pekin duckling. Poult Sci 2005;84:426–31.
https://doi.org/10.1093/ps/84.3.426
75. Ru M, Wang W, Zhai Z, et al. Nicotinamide mononucleotide supplementation protects the intestinal function in aging mice and D-galactose induced senescent cells. Food Funct 2022;13:7507–19.
https://doi.org/10.1039/D2FO00525E
78. Epple HJ, Friebel J, Moos V, et al. Architectural and functional alterations of the small intestinal mucosa in classical Whipple’s disease. Mucosal Immunol 2017;10:1542–52.
https://doi.org/10.1038/mi.2017.6
79. Koehler P, Wieser H, Scherf KA. Celiac disease. Kırtıl E, Kılercıoglu M, Öztop HM, editorsReference module in food science. Elsevier; 2016.
82. Piovezana Bossolani GD, Silva BT, Colombo Martins Perles JV, et al. Rheumatoid arthritis induces enteric neurodegeneration and jejunal inflammation, and quercetin promotes neuroprotective and anti-inflammatory actions. Life Sci 2019;238:116956.
https://doi.org/10.1016/j.lfs.2019.116956
84. Hang CH, Shi JX, Sun BW, Li JS. Apoptosis and functional changes of dipeptide transporter (PepT1) in the rat small intestine after traumatic brain injury. J Surg Res 2007;137:53–60.
https://doi.org/10.1016/j.jss.2006.06.026
85. Chen YM, Helm ET, Groeltz-Thrush JM, Gabler NK, Burrough ER. Epithelial-mesenchymal transition of absorptive enterocytes and depletion of Peyer’s patch M cells after PEDV infection. Virology 2021;552:43–51.
https://doi.org/10.1016/j.virol.2020.08.018
86. Madson DM, Magstadt DR, Arruda PHE, et al. Pathogenesis of porcine epidemic diarrhea virus isolate (US/Iowa/18984/ 2013) in 3-week-old weaned pigs. Vet Microbiol 2014;174:60–8.
https://doi.org/10.1016/j.vetmic.2014.09.002
88. Wang D, Zhou X, She R, et al. Impaired intestinal mucosal immunity in specific-pathogen-free chickens after infection with very virulent infectious bursal disease virus. Poult Sci 2009;88:1623–8.
https://doi.org/10.3382/ps.2009-00124
89. Feng GD, He J, Ao X, Chen DW. Effects of maize naturally contaminated with aflatoxin B1 on growth performance, intestinal morphology, and digestive physiology in ducks. Poult Sci 2017;96:1948–55.
https://doi.org/10.3382/ps/pew420
94. Huang L, Chiang Chiau JS, Cheng ML, et al. SCID/NOD mice model for 5-FU induced intestinal mucositis: safety and effects of probiotics as therapy. Pediatr Neonatol 2019;60:252–60.
https://doi.org/10.1016/j.pedneo.2018.07.007
96. Yi D, Liu W, Hou Y, et al. Establishment of a porcine model of indomethacin-induced intestinal injury. Front Biosci (Landmark Ed) 2018;23:2166–76.
https://doi.org/10.2741/4697
97. Tian J, Washizawa N, Gu LH, et al. Local glutathione redox status does not regulate ileal mucosal growth after massive small bowel resection in rats. J Nutr 2007;137:320–5.
https://doi.org/10.1093/jn/137.2.320
99. Toth S, Jonecova Z, Maretta M, et al. The effect of betanin parenteral pretreatment on jejunal and pulmonary tissue histological architecture and inflammatory response after jejunal ischemia-reperfusion injury. Exp Mol Pathol 2019;110:104292.
https://doi.org/10.1016/j.yexmp.2019.104292
100. Xie D, Li J, Wang ZX, et al. Effects of monochromatic light on mucosal mechanical and immunological barriers in the small intestine of broilers. Poult Sci 2011;90:2697–704.
https://doi.org/10.3382/ps.2011-01416
101. Barri A, Honaker CF, Sottosanti JR, Hulet RM, McElroy AP. Effect of incubation temperature on nutrient transporters and small intestine morphology of broiler chickens. Poult Sci 2011;90:118–25.
https://doi.org/10.3382/ps.2010-00908
103. Gogoi S, Kolluri G, Tyagi JS, Marappan G, Manickam K, Narayan R. Impact of heat stress on broilers with varying body weights: elucidating their interactive role through physiological signatures. J Therm Biol 2021;97:102840.
https://doi.org/10.1016/j.jtherbio.2021.102840
104. Palander PA, Heinonen M, Simpura I, Edwards SA, Valros AE. Jejunal morphology and blood metabolites in tail biting, victim and control pigs. Animal 2013;7:1523–31.
https://doi.org/10.1017/S1751731113000669
105. He Y, Liu N, Ji Y, Tso P, Wu Z. Weaning stress in piglets alters the expression of intestinal proteins involved in fat absorption. J Nutr 2022;152:2387–95.
https://doi.org/10.1093/jn/nxac177