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Effects of Achyranthes Bidentata Polysaccharide on Growth Performance, Immunological, Adrenal, and Somatotropic Responses of Weaned Pigs Challenged with Escherichia coli Lipopolysaccharide

  • Guo, Guanglun (Hubei Key Laboratory of Animal Nutrition and Feed Science, Wuhan Polytechnic University) ;
  • Liu, Yulan (Hubei Key Laboratory of Animal Nutrition and Feed Science, Wuhan Polytechnic University) ;
  • Fan, Wei (Hubei Key Laboratory of Animal Nutrition and Feed Science, Wuhan Polytechnic University) ;
  • Han, Jie (Hubei Key Laboratory of Animal Nutrition and Feed Science, Wuhan Polytechnic University) ;
  • Hou, Yongqing (Hubei Key Laboratory of Animal Nutrition and Feed Science, Wuhan Polytechnic University) ;
  • Yin, Yulong (Hubei Key Laboratory of Animal Nutrition and Feed Science, Wuhan Polytechnic University) ;
  • Zhu, Huiling (Hubei Key Laboratory of Animal Nutrition and Feed Science, Wuhan Polytechnic University) ;
  • Ding, Binying (Hubei Key Laboratory of Animal Nutrition and Feed Science, Wuhan Polytechnic University) ;
  • Shi, Junxia (Hubei Key Laboratory of Animal Nutrition and Feed Science, Wuhan Polytechnic University) ;
  • Lu, Jing (Hubei Key Laboratory of Animal Nutrition and Feed Science, Wuhan Polytechnic University) ;
  • Wang, Huirong (Hubei Key Laboratory of Animal Nutrition and Feed Science, Wuhan Polytechnic University) ;
  • Chao, Jin (Hubei Key Laboratory of Animal Nutrition and Feed Science, Wuhan Polytechnic University) ;
  • Qu, Yonghua (Hubei Key Laboratory of Animal Nutrition and Feed Science, Wuhan Polytechnic University)
  • Received : 2007.12.20
  • Accepted : 2008.03.17
  • Published : 2008.08.01

Abstract

A study was conducted with 48 weaned barrows ($28{\pm}3d$, $8.45{\pm}0.14kg$) to determine the effect of Achyranthes bidentata polysaccharide (ABPS) supplementation on pig performance, immunological, adrenal and somatotropic responses following Escherichia coli lipopolysaccharide (LPS) challenge. The experiment was a $2{\times}2$ factorial design; the main factors included diet (supplementation with 0 or 500 mg/kg ABPS) and immunological challenge (LPS or saline). On d 14 and 21 of the trial, pigs were given an intraperitoneal injection with either $100{\mu}g/kg$ BW of LPS or an equivalent amount of sterile saline. Blood samples were obtained 3 h after injection for analysis of tumor necrosis factor-${\alpha}$ (TNF-${\alpha}$), prostaglandin $E_2$ ($PGE_2$), cortisol, growth hormone (GH), insulin-like growth factor (IGF)-I and immunoglobulin G (IgG). On d 2 after LPS challenge, peripheral blood lymphocyte proliferation (PBLP) was measured. LPS administration decreased average daily feed intake (ADFI) (p<0.05), had a tendency to decrease average daily gain (ADG) (p<0.10) during both the first and second challenge periods and increased (p<0.05) feed:gain ratio only during the first challenge period. ABPS tended to improve ADG (p<0.10) during the first challenge period, and improved ADG (p<0.05) and tended to improve ADFI (p<0.10) during the second challenge period. ABPS did not affect feed:gain ratio. An interaction (p<0.05) between LPS challenge and diet was observed for the plasma concentrations of TNF-${\alpha}$, $PGE_2$ and cortisol after both LPS challenges such that, among LPS-treated pigs, pigs fed the ABPS diet were lower for these indices than those receiving the control diet. In contrast, pigs fed the ABPS diet had higher IGF-I (p<0.05) compared with those fed the control diet. No effect of diet, LPS challenge or both on GH and IgG was observed after both LPS administrations. LPS challenge increased PBLP when these cells were incubated with $8{\mu}g/ml$ of LPS during both the challenge periods, and did likewise when incubated with $8{\mu}g/ml$ of concanavalin A only after the first challenge. ABPS had no effect on PBLP. These data demonstrate that ABPS alters the release of pro-inflammatory cytokines following an immunological challenge, which might enable pigs to achieve better performance.

Keywords

References

  1. Calder, P. C. 1997. n-3 Polyunsaturated fatty acids and immune cell function. Adv. Enzyme Reg. 37:197-237. https://doi.org/10.1016/S0065-2571(96)00004-0
  2. Chen, H. L. 2002. Studies on the extraction, immunomodulating activities of Chinese Herbal polysaccharides and approach to the mechanism. Ph.D. Dissertation, Chinese Academy of Agriculture Science, Beijing, China.
  3. Chen, X, M., Y. J. Xu and G.. Y. Tian. 2005. Physical-chemical properties and structure elucidation of ABPS isolated from the root of achyranthes bidentata. Acta Pharm Sinica 40:32-35 (Chinese).
  4. George, P. and M. D. Chrousos. 1995. The hypothalamic-pituitaryadrenal axis and immune-mediated inflammation. N. Engl. J. Med. 332:1351-1363. https://doi.org/10.1056/NEJM199505183322008
  5. Hasselgren, P. O. 1993. Protein metabolism in sepsis. R. G. Landes Co., Austin, TX.
  6. Hellerstein, M. K., S. N. Meydani, M. Meydani, K. Wu and C. A. Dinarello. 1989. Interleukin-1 induced anorexia in the rat. Influence of prostaglandins. J. Clin. Invest. 84:228-235. https://doi.org/10.1172/JCI114145
  7. Hicks, T. A., J. J. McGlone, C. S. Whisnant, H. G. Kattesh and R. L. Norman. 1998. Behavioral, endocrine, immune, and performance measures for pigs exposed to acute stress. J. Anim. Sci. 76:474-483. https://doi.org/10.2527/1998.762474x
  8. Hoqaboam, C. M., M. L. Steinhauser, H. Schock, N. Lukacs, H. Schock, N. Lukacs, R. M. Strieter, T. Standiford and S. L. Kunkel. 1998. Therapeutic effects of nitric oxide inhibition during experimental fecal peritonitis: Role of interleukin-10 and monocyte chemoattractant protein 1. Infect. Immun. 66:650-655.
  9. Jin, L. Q., Z. J. Zheng, Y. Peng, W. X. Li, X. M. Chen and J. X. Lu. 2007. Opposite effects on tumor growth depending on dose of achyranthes bidentata polysaccharides in C57BL/6 mice. Int. Immunopharmacol. 7:568-577. https://doi.org/10.1016/j.intimp.2006.12.009
  10. Johnson, R. W. 1997. Inhibition of growth by pro-inflammatory cytokines: An integrated view. J. Anim. Sci. 75:1244-1255. https://doi.org/10.2527/1997.7551244x
  11. Johnson, R. W. and E. von Borell. 1994. Lipopolysaccharideinduced sickness behavior in pigs is inhibited by pretreatment with indomethacin. J. Anim. Sci. 72:309-314. https://doi.org/10.2527/1994.722309x
  12. Kelley, K. W., R. W. Johnson and R. Dantzer. 1994. Immunology discovers physiology. Vet. Immunol. Immunopathol. 43:157-165. https://doi.org/10.1016/0165-2427(94)90132-5
  13. Kong, X. F., Y. L. Yin, G. Y. Wu, H. J. Liu, F. G. Yin, T. J. Li, R. L. Huang, Z. Ruan, H. Xiong, Z. Y. Deng, M. Y. Xie, Y. P. Liao and S. W. Kim. 2007. Dietary supplementation with acanthopanax senticosus extract modulates cellular and humoral immunity in weaned piglets. Asian-Aust. J. Anim. Sci. 20:1453-1461. https://doi.org/10.5713/ajas.2007.1453
  14. Lang, C. H., J. Fan, R. Cooney and T. C. Vary. 1996. Interleukin-1 receptor antagonist attenuates sepsis-induced alterations in the IGF system and protein synthesis. Am. J. Physiol. 270:E430-E437.
  15. Lee, D. N., T. F. Shen, H. T. Yen, C. F. Weng and B. J. Chen. 2000a. Effects of chromium supplementation and lipopolysaccharide injection on the immune responses of weanling pigs. Asian-Aust. J. Anim. Sci. 13:1414-1421. https://doi.org/10.5713/ajas.2000.1414
  16. Lee, D. N., C. F. Weng, H. T. Yen, T. F. Shen and B. J. Chen. 2000b. Effects of chromium supplementation and lipopolysaccharide injection on physiological responses of weanling pigs. Asian-Aust. J. Anim. Sci. 13:528-534. https://doi.org/10.5713/ajas.2000.528
  17. Li, Z. K. and D. D. Li. 1997. The immunomodulatory effect of achyranthes bidentata polysaccharides. Acta Pharm Sinica 32:881-887 (Chinese).
  18. Lien, T. F., K. H. Yang and K. J. Lin. 2005. Effects of chromium propionate supplementation on growth performance, serum traits and immune response in weaned pigs. Asian-Aust. J. Anim. Sci. 18:403-408. https://doi.org/10.5713/ajas.2005.403
  19. Liu, Y. L., J. J. Huang, Y. Q. Hou, H. L. Zhu, S. J. Zhao, B. Y. Ding, Y. L. Yin, G. F. Yi, J. X. Shi and W. Fan. 2008a. Dietary arginine supplementation alleviates intestinal mucosal disruption induced by Escherichia coli lipopolysaccharide in weaned pigs. Br. J. Nutr. doi:10.1017/S0007114508911612.
  20. Liu, Y. L., D. F. Li, L. M. Gong, Z. Y. Feng, G. F. Yi, A. M. Gaines and J. A. Carroll. 2003. Effects of fish oil supplementation on performance as well as immunological, adrenal and somatotropic responses of weaned pigs after Escherichia coli lipopolysaccharide challenge. J. Anim. Sci. 81:2758-2765. https://doi.org/10.2527/2003.81112758x
  21. Liu, Y. L., J. Lu, J. X. Shi, Y. Q. Hou, H. L. Zhu, S. J. Zhao, H. M. Liu, B. Y. Ding, Y. L. Yin and G. F. Yi. 2008b. Increased expression of the peroxisome proliferator-activated receptor $\gamma$ in the immune system of weaned pigs after Escherichia coli lipopolysaccharide challenge. Vet. Immunol. Immunopathol. 10.1016/j.vetimm.2008.02.014.
  22. Mandrup-Poulsen, T., J. Nerup, J. I. Reimers, F. Pociot, H. U. Anderson, A. Karlsen, U. Bjerre and R. Bergholdt. 1995. Cytokines and the endocrine system. I. The immunoendocrine network. Eur. J. Endocrinol. 133:660-671. https://doi.org/10.1530/eje.0.1330660
  23. Mao, X. F., X. S. Piao, C. H. Lai, D. F. Li, J. J. Xing and B. L. Shi. 2005. Effects of $\beta$-glucan obtained from the Chinese herb Astragalus membranaceus and lipopolysaccharide challenge on performance, immunological, adrenal, and somatotropic responses of weanling pigs. J. Anim. Sci. 83:2775-2782. https://doi.org/10.2527/2005.83122775x
  24. McCarthy, H. D., S. Dryden and G. Williams. 1995. Interleukin-1 $\beta$-induced anorexia and pyrexia in rat: Relationship to hypothalamic neuropeptide Y. Am. J. Physiol. 269:E852-E857.
  25. Perlstein, R. S., M. H. Whitnall, J. S. Abrams, E. H. Mougey and R. Neta. 1993. Synergistic roles of interleukin-6, interleukin-1, and tumor necrosis factor in the adrenocorticotropin response to bacterial lipopolysaccharide in vivo. Endocrinol. 132:946-952. https://doi.org/10.1210/en.132.3.946
  26. Poutsiaka, D. D., M. Mengozzi, B. Sinha and C. A. Dinarello. 1993. Cross-linking of the beta-glucan receptor on human monocytes results in interleukin-1 receptor antagonist but not interleukin-1 production. Blood 82:3695-3700.
  27. Schottelius, A. J. G., M. W. Mayo, R. B. Sartor and A. S. Baldwin, Jr. 1999. Interleukin-10 signaling blocks inhibitor of kappa B kinase activity and nuclear factor kappa B DNA binding. J. Biol. Chem. 274:31868-31874. https://doi.org/10.1074/jbc.274.45.31868
  28. Shao, S. J., L. Mai and Y. Chen. 2002. The effect of achyranthes bidentata polysaccharide on mice red blood cell immunological function. Chinese Remedies and Clinics, 5:281-282 (Chinese).
  29. Soto, L., A. I. Martin, S. Millan, E. Vara and A. Lopez-Calderon. 1998. Effects of endotoxin lipopolysaccharide administration on the somatotropic axis. J. Endocrinol. 159:239-246. https://doi.org/10.1677/joe.0.1590239
  30. Spurlock, M. E. 1997. Regulation of metabolism and growth during immune challenge: An overview of cytokine function. J. Anim. Sci. 75:1773-1783. https://doi.org/10.2527/1997.7571773x
  31. Webel, D. M., B. N. Finck, D. H. Baker and R. W. Johnson. 1997. Time course of increased plasma cytokines, cortisol, and urea nitrogen in pigs following intraperitoneal injection of lipopolysaccharide. J. Anim. Sci. 75:1514-1520. https://doi.org/10.2527/1997.7561514x

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