Browse > Article
http://dx.doi.org/10.5713/ajas.2008.70739

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)
Publication Information
Asian-Australasian Journal of Animal Sciences / v.21, no.8, 2008 , pp. 1189-1195 More about this Journal
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
Achyranthes Bidentata Polysaccharide; Lipopolysaccharide; Inflammatory Response; Weaned Pigs;
Citations & Related Records
Times Cited By KSCI : 2  (Citation Analysis)
Times Cited By Web Of Science : 10  (Related Records In Web of Science)
Times Cited By SCOPUS : 10
연도 인용수 순위
1 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.   DOI   ScienceOn
2 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.   DOI
3 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.   DOI   ScienceOn
4 Spurlock, M. E. 1997. Regulation of metabolism and growth during immune challenge: An overview of cytokine function. J. Anim. Sci. 75:1773-1783.   DOI
5 George, P. and M. D. Chrousos. 1995. The hypothalamic-pituitaryadrenal axis and immune-mediated inflammation. N. Engl. J. Med. 332:1351-1363.   DOI   ScienceOn
6 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.   과학기술학회마을   DOI
7 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.   DOI
8 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.   DOI   ScienceOn
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.   DOI   ScienceOn
10 Johnson, R. W. 1997. Inhibition of growth by pro-inflammatory cytokines: An integrated view. J. Anim. Sci. 75:1244-1255.   DOI
11 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.   DOI
12 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.
13 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.   DOI
14 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.
15 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.   DOI
16 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).
17 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.
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.   과학기술학회마을   DOI
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.   DOI   ScienceOn
20 Li, Z. K. and D. D. Li. 1997. The immunomodulatory effect of achyranthes bidentata polysaccharides. Acta Pharm Sinica 32:881-887 (Chinese).
21 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.   DOI
22 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.   DOI
23 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.
24 Kelley, K. W., R. W. Johnson and R. Dantzer. 1994. Immunology discovers physiology. Vet. Immunol. Immunopathol. 43:157-165.   DOI   ScienceOn
25 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.   DOI
26 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).
27 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.   DOI
28 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.
29 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.   DOI
30 Hasselgren, P. O. 1993. Protein metabolism in sepsis. R. G. Landes Co., Austin, TX.
31 Calder, P. C. 1997. n-3 Polyunsaturated fatty acids and immune cell function. Adv. Enzyme Reg. 37:197-237.   DOI   ScienceOn