Indian Journal of Animal Research

  • Chief EditorK.M.L. Pathak

  • Print ISSN 0367-6722

  • Online ISSN 0976-0555

  • NAAS Rating 6.50

  • SJR 0.263

  • Impact Factor 0.4 (2024)

Frequency :
Monthly (January, February, March, April, May, June, July, August, September, October, November and December)
Indexing Services :
Science Citation Index Expanded, BIOSIS Preview, ISI Citation Index, Biological Abstracts, Scopus, AGRICOLA, Google Scholar, CrossRef, CAB Abstracting Journals, Chemical Abstracts, Indian Science Abstracts, EBSCO Indexing Services, Index Copernicus
Indian Journal of Animal Research, volume 53 issue 2 (february 2019) : 239-244

Microstructural changes and immunohistological analysis of pro-inflammatory cytokines in spleens of lipopolysaccharide-induced rats

Y.B. Zhong, X.L. Zhang, M.Y. Lv, X.F. Hu, Y. Li
1College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang 330 045, Jiangxi, China.
Cite article:- Zhong Y.B., Zhang X.L., Lv M.Y., Hu X.F., Li Y. (2018). Microstructural changes and immunohistological analysis of pro-inflammatory cytokines in spleens of lipopolysaccharide-induced rats. Indian Journal of Animal Research. 53(2): 239-244. doi: 10.18805/ijar.B-897.
This study investigated splenic status changes in weaned Sprague-Dawley rats induced by lipopolysaccharide. There were forty 26-day-old rats selected randomly and equally divided into two groups. The treatment group received daily single doses of lipopolysaccharide, and the control group was treated with normal saline. We conducted haematoxylin-eosin staining, immunohistochemical staining and semi-quantitative optical density analysis for both groups on the 29th, 32nd, 35th and 38th days after treatment. The results indicated that splenic marginal zone in the lipopolysaccharide group was thinner or disappeared compared to that of the saline group. However, the periarterial lymphoid sheath and the diameters of splenic lymphoid follicles appeared thicker and wider than those in the saline group (P<0.05). The expression of interleukin-1 beta, interleukin-6 and tumour necrosis factor alpha was mainly localized within the periarterial lymphoid sheath and splenic lymphoid follicles in the lipopolysaccharide treated rats. The integrated optical density and the average optical density in the lipopolysaccharide group were greater than those in the normal saline treated group (P<0.05). In conclusion, splenic immune function is probably strengthened by altering microstructures and releasing pro-inflammatory cytokines following lipopolysaccharide treatment.
  1. Bachmann M.F. and Oxenius A. (2007). Interleukin 2: from immunostimulation to immunoregulation and back again. EMBO Reports, 8:1142-1148.
  2. Cen Y., Liu C., Li X., Yan Z., Kuang M., Su Y., Pan X., Qin R., Liu X., Zheng J., Zhou H. (2016). Artesunate ameliorates severe acute pancreatitis (SAP) in rats by inhibiting expression of pro-inflammatory cytokines and Toll-like receptor 4. International Immunopharmacology, 38:252-260.
  3. Dantzer R., O’Connor J.C., Freund G.G., Johnson R.W., Kelley K.W. (2008). From inflammation to sickness and depression: when the immune system subjugates the brain. Nature Reviews Neuroscience, 9:46-56.
  4. Dellagioia N. and Hannestad J. (2010). A critical review of human endotoxin administration as an experimental paradigm of depression. Neuroscience & Biobehavioral Reviews, 34:130-143.
  5. Dhabhar F.S., Malarkey W.B., Neri E., McEwen B.S. (2012). Stress-induced redistribution of immune cells—from barracks to boulevards to battlefields: a tale of three hormones-Curt Richter Award winner. Psychoneuroendocrinology, 37:1345-1368. 
  6. Du Q., Wang C., Zhang N., Li G., Zhang M., Li L., Zhang Q., Zhang J. (2014). In vivo study of the effects of exogenous hydrogen sulfide on lung mitochondria in acute lung injury in rats. BMC Anesthesiology, 14:117.
  7. Good-Jacobson K.L., Song E., Anderson S., Sharpe A.H., Shlomchik M.J. (2012). CD80 expression on B cells regulates murine T follicular helper development, germinal center B cell survival, and plasma cell generation. Journal of Immunology, 188:4217-4225.
  8. Huang H., Liu A., Wu H., Ansari A.R., Wang J., Huang X., Zhao X., Peng K., Zhong J., Liu H. (2016). Transcriptome analysis indicated that Salmonella lipopolysaccharide-induced thymocyte death and thymic atrophy were related to TLR4-FOS/JUN pathway in chicks. BMC Genomics, 17:322.
  9. Ikezoe T., Yang Y., Heber D., Taguchi H., Koeffler H.P. (2003). PC-SPES: a potent inhibitor of nuclear factor-kappa B rescues mice from lipopolysaccharide-induced septic shock. Molecular Pharmacology, 64:1521-1529.
  10. Meseguer V., Alpizar Y.A., Luis E., Tajada S., Denlinger B., Fajardo O., Manenschijn J.A et al (2014). TRPA1 channels mediate acute neurogenic inflammation and pain produced by bacterial endotoxins. Nature Communications, 5:3125.
  11. Miller A.H., Maletic V., Raison C.L. (2009). Inflammation and its discontents: the role of cytokines in the pathophysiology of major depression. Biological Psychiatry, 65:732-741.
  12. Peri F., Piazza M., Calabrese V., Damore G., Cighetti R. (2010). Exploring the LPS/TLR4 signal pathway with small molecules. Biochemical Society Transactions, 38:1390-1395.
  13. Rietschel E.T. and Brade H. (1992). Bacterial endotoxins. Scientific American, 267:54-61.
  14. Schiepers O.J., Wichers M.C., Maes M. (2005). Cytokines and major depression. Prog. Neuropsychopharmacol. Biological Psychiatry, 29:201-217.
  15. Slavich G.M. and Irwin M.R. (2014). From stress to inflammation and major depressive disorder: a social signal transduction theory of depression. Psychological bulletin, 140:774-815.
  16. Tough D.F., Sun S., Sprent J. (1997). T cell stimulation in vivo by lipopolysaccharide (LPS). Journal of Experimental Medicine, 185:2089-2094.
  17. Verstrepen L., Bekaert T., Chau T.L., Tavernier J., Chariot A., Beyaert R. (2008). TLR-4, IL-1R and TNF-R signaling to NF-kappaB: variations on a common theme. Cellular and Molecular Life Sciences, 65:2964-2978.
  18. Xiao K., Zou W.H., Yang Z., Zia U.R., Ansari A.R., Yuan H.R., Zhou Y., Cui L., Peng K.M., Song H. (2015). The role of visfatin on the regulation of inflammation and apoptosis in the spleen of LPS-treated rats. Cell and Tissue Research, 359:605-618.
  19. Zheng B., Han S., Kelsoe G. (1996). T helper cells in murine germinal centers are antigen-specific emigrants that downregulate Thy-    1. Journal of Experimental Medicine, 184:1083-1091.
  20. Zhong Y., Hu X., Guo H., Li Y. (2017). Skp2 expression exhibits a negative correlation with P27Kip1 in lungs of SD rat stress model induced by lipopolysaccharide. Indian Journal of Animal Research, 51:1019-1026.
  21. Zong X., Hu W., Song D., Li Z., Du H., Lu Z., Wang Y. (2016). Porcine lactoferrin-derived peptide LFP-20 protects intestinal barrier by maintaining tight junction complex and modulating inflammatory response. Biochemical Pharmacology, 104:74-82. 

Editorial Board

View all (0)