DOI QR코드

DOI QR Code

Effects of quercetin and coated sodium butyrate dietary supplementation in diquat-challenged pullets

  • Zhou, Ning (College of Animal Science and Technology, Nanjing Agricultural University) ;
  • Tian, Yong (State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products, Institute of Animal Science & Veterinary, Zhejiang Academy of Agricultural Sciences) ;
  • Liu, Wenchao (Huzhou Lvchang Ecoagriculture Co., Ltd.) ;
  • Tu, Bingjiang (Huzhou Wuxing District Animal Disease Prevention and Control Center) ;
  • Gu, Tiantian (State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products, Institute of Animal Science & Veterinary, Zhejiang Academy of Agricultural Sciences) ;
  • Xu, Wenwu (State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products, Institute of Animal Science & Veterinary, Zhejiang Academy of Agricultural Sciences) ;
  • Zou, Kang (College of Animal Science and Technology, Nanjing Agricultural University) ;
  • Lu, Lizhi (College of Animal Science and Technology, Nanjing Agricultural University)
  • 투고 : 2021.11.01
  • 심사 : 2022.03.02
  • 발행 : 2022.09.01

초록

Objective: This study was designed to investigate the hypothesis that dietary quercetin (QUE) and coated sodium butyrate (SB) supplementation alleviate oxidative stress in the small intestine of diquat (DIQ)-challenged pullets. Methods: A total of 200 13-week-old pullets were divided into four groups: the control group (CON), the DIQ group, the QUE group, and the coated SB group, and injected intraperitoneally with either saline (CON) or diquat (DIQ, QUE, and SB) to induce oxidative stress on day 0. Results: On the first day, the malondialdehyde and superoxide dismutase (SOD) concentrations in the SB group were significantly different from those in the DIQ and QUE groups (p<0.05), and dietary supplementation with SB increased serum glutathione peroxidase (GSH-PX) levels compared with the DIQ group (p<0.05). Quercetin and SB increased the levels of CLAUDIN-1 and zonula occludens-1 (ZO-1) in the jejunum. On the tenth day of treatment, QUE attenuated the decrease in GSH-PX levels compared to those of the CON group (p<0.05), while SB increased SOD, GSH-PX, and total antioxidant capacity levels compared to those of the DIQ group. Nuclear factor erythroid 2-related factor 2 (NRF2) and heme oxygenase-1 (HO-1) mRNA levels in the QUE and SB groups increased (p<0.05) and CLAUDIN-1 mRNA levels in the QUE and SB groups were upregulated compared to those in the DIQ group ileum tissue. Conclusion: Supplementation of QUE and SB demonstrated the ability to relieve oxidative stress in pullets post DIQ-injection with a time-dependent manner and QUE and SB may be potential antioxidant additives for relieving oxidative stress and protecting the intestinal barrier of pullets.

키워드

과제정보

This work was supported by Zhejiang Provincial Key Research and Development Plan (Grant NO. 2021C02034), Zhejiang Provincial Team Special Commissioner Project of Science and Technology (Xianju Chicken Industry, 2020-2024) and the agricultural (livestock and poultry) new breed selection and breeding major science and technology special projects of Zhejiang Province (2021C02068).

참고문헌

  1. Frankic T, Salobir K, Salobir J. The comparison of in vivo antigenotoxic and antioxidative capacity of two propylene glycol extracts of Calendula officinalis (marigold) and vitamin E in young growing pigs. J Anim Physiol Anim Nutr 2009;93: 688-94. https://doi.org/10.1111/j.1439-0396.2008.00855.x
  2. Celi P, Trana AD, Claps S. Effects of plane of nutrition on oxidative stress in goats during the peripartum period. Vet J 2010;184:95-9. https://doi.org/10.1016/j.tvjl.2009.01.014
  3. Mishra B, Jha R. Oxidative stress in the poultry gut: potential challenges and interventions. Front Vet Sci 2019;6:60. https://doi.org/10.3389/fvets.2019.00060
  4. Wang Y, Wu YP, Wang YB, et al. Bacillus amyloliquefaciens SC06 alleviates the oxidative stress of IPEC-1 via modulating Nrf2/Keap1 signaling pathway and decreasing ROS production. Appl Microbiol Biotechnol 2017;101:3015-26. https://doi.org/10.1007/s00253-016-8032-4
  5. Li YH, Hansen SL, Borst LB, et al. Dietary iron deficiency and oversupplementation increase intestinal permeability, ion transport, and inflammation in pigs. J Nutr 2016;146: 1499-505. https://doi.org/10.3945/jn.116.231621
  6. Mitic LL, Van Itallie CM, Anderson JM. Molecular physiology and pathophysiology of tight junctions I. Tight junction structure and function: lessons from mutant animals and proteins. Am J Physiol Gastrointest Liver Physiol 2000;279: G250-4. https://doi.org/10.1152/ajpgi.2000.279.2.G250
  7. Cao ST, Wu H, Wang CC, et al. Diquat-induced oxidative stress increases intestinal permeability, impairs mitochondrial function, and triggers mitophagy in piglets. J Anim Sci 2018; 96:1795-805. https://doi.org/10.1093/jas/sky104
  8. Li M, Yuan DX, Liu YH, Jin H, Tan B. Dietary puerarin supplementation alleviates oxidative stress in the small intestines of diquat-challenged piglets. Animals (Basel) 2020;10:631. https://doi.org/10.3390/ani10040631
  9. Chen YN, Chen YP, Zhang H, Wang T. Pterostilbene as a protective antioxidant attenuates diquat-induced liver injury and oxidative stress in 21-day-old broiler chickens. Poult Sci 2020;99:3158-67. https://doi.org/10.1016/j.psj.2020.01.021
  10. Yuan DX, Hussain T, Tan B, Liu YH, Ji P, Yin YL. The evaluation of antioxidant and anti-inflammatory effects of eucommia ulmoides flavones using diquat-challenged piglet models. Oxid Med Cell Longev 2017;2017:8140962. https://doi.org/10.1155/2017/8140962
  11. Wang SG, Yao JY, Zhou B, et al. Bacteriostatic effect of quercetin as an antibiotic alternative in vivo and its antibacterial mechanism in vitro. J Food Prot 2018;81:68-78. https://doi.org/10.4315/0362-028X.JFP-17-214
  12. Luo MJ, Tian R, Yang ZY, Peng YY, Lu NH. Quercetin suppressed NADPH oxidase-derived oxidative stress via heme oxygenase-1 induction in macrophages. Arch Biochem Biophys 2019;671:69-76. https://doi.org/10.1016/j.abb.2019.06.007
  13. Dong YY, Lei JQ, Zhang BK. Effects of dietary quercetin on the antioxidative status and cecal microbiota in broiler chickens fed with oxidized oil. Poult Sci 2020;99:4892-903. https://doi.org/10.1016/j.psj.2020.06.028
  14. Sun L, Xu GQ, Dong YYY, Li M, Yang LY, Lu WF. Quercetin protects against lipopolysaccharide-induced intestinal oxidative stress in broiler chickens through activation of Nrf2 pathway. Molecules 2020;25:1053. https://doi.org/10.3390/molecules25051053
  15. Chang PV, Hao LM, Offermanns S, Medzhitov R. The microbial metabolite butyrate regulates intestinal macrophage function via histone deacetylase inhibition. Proc Natl Acad Sci USA 2014;111:2247-52. https://doi.org/10.1073/pnas.1322269111
  16. Kanai T, Mikami Y, Hayashi A. A breakthrough in probiotics: Clostridium butyricum regulates gut homeostasis and antiinflammatory response in inflammatory bowel disease. J Gastroenterol 2015;50:928-39. https://doi.org/10.1007/s00535-015-1084-x
  17. Song BC, Li HX, Wu YY, et al. Effect of microencapsulated sodium butyrate dietary supplementation on growth performance and intestinal barrier function of broiler chickens infected with necrotic enteritis. Anim Feed Sci Technol 2017; 232:6-15. https://doi.org/10.1016/j.anifeedsci.2017.07.009
  18. Zhang WH, Gao F, Zhu QF, et al. Dietary sodium butyrate alleviates the oxidative stress induced by corticosterone exposure and improves meat quality in broiler chickens. Poult Sci 2011;90:2592-9. https://doi.org/10.3382/ps.2011-01446
  19. Zou X, Ji J, Qu H, et al. Effects of sodium butyrate on intestinal health and gut microbiota composition during intestinal inflammation progression in broilers. Poult Sci 2019;98: 4449-56. https://doi.org/10.3382/ps/pez279
  20. Wen CY, Guo QP, Wang WL, et al. Taurine alleviates intestinal injury by mediating tight junction barriers in diquat-challenged piglet models. Front Physiol 2020;11:449. https://doi.org/10.3389/fphys.2020.00449
  21. Kim SJ, Kim GH. Quantification of quercetin in different parts of onion and its DPPH radical scavenging and antibacterial activity. Food Sci Biotechnol 2006;15:39-43.
  22. Zou Y, Wei HK, Xiang QH, Wang J, Zhou YF, Peng J. Protective effect of quercetin on pig intestinal integrity after transport stress is associated with regulation oxidative status and inflammation. J Vet Med Sci 2016;78:1487-94. https://doi.org/10.1292/jvms.16-0090
  23. Liu WH, La ALTZ, Evans A, et al. Supplementation with sodium butyrate improves growth and antioxidant function in dairy calves before weaning. J Anim Sci Biotechnol 2021; 12:2. https://doi.org/10.1186/s40104-020-00521-7
  24. Hao LH, Cheng YZ, Su WF, et al. Pediococcus pentosaceus ZJUAF-4 relieves oxidative stress and restores the gut microbiota in diquat-induced intestinal injury. Appl Microbiol Biotechnol 2021;105:1657-68. https://doi.org/10.1007/s00253-021-11111-6
  25. Suzuki T, Motohashi H, Yamamoto M. Toward clinical application of the Keap1-Nrf2 pathway. Trends Pharmacol Sci 2013;34:340-6. https://doi.org/10.1016/j.tips.2013.04.005
  26. Liu L, Wu CM, Chen DW, et al. Selenium-enriched yeast alleviates oxidative stress-induced intestinal mucosa disruption in weaned pigs. Oxid Med Cell Longev 2020;2020:5490743. https://doi.org/10.1155/2020/5490743
  27. Entaz B, Kim JY, Yoon H. Quercetin attenuates manganeseinduced neuroinflammation by alleviating oxidative stress through regulation of apoptosis, iNOS/NF-κB and HO-1/Nrf2 pathways. Int J Mol Sci 2017;18:1989. https://doi.org/10.3390/ijms18091989
  28. Ma N, Ahamed AJ, Shahid BM, Dai HY, Shen XZ. Sodium butyrate improves antioxidant stability in sub-acute ruminal acidosis in dairy goats. BMC Vet Res 2018;14:275. https://doi.org/10.1186/s12917-018-1591-0
  29. Anderson JM, Van Itallie CM. Tight junctions and the molecular basis for regulation of paracellular permeability. Am J Physiol Gastrointest Liver Physiol 1995;269:G467-75. https://doi.org/10.1152/ajpgi.1995.269.4.G467
  30. Zhang K, Meng MJ, Gao LP, Tu YL, Bai YF. Sodium butyrate improves high-concentrate-diet-induced impairment of ruminal epithelium barrier function in goats. J Agric Food Chem 2018;66:8729-36. https://doi.org/10.1021/acs.jafc.8b0310