Inhibitory effects of astragalin on lipopolysaccharide-induced inflammatory response in mouse mammary epithelial cells

Journal of Surgical Research

Volumn 192, Issue 2, 2014, Pages 573-581

  Li, Fengyang ^a   Wang, Wei ^a   Cao, Yongguo ^a   Liang, Dejie ^a   Zhang, Wenlong ^a   Zhang, Zecai ^a   Jiang, Haichao ^a   Guo, Mengyao ^a   Zhang, Naisheng ^a  

^a JILIN UNIVERSITY   (China)

Author keywords

Astragalin; Cytokine; LPS; Mastitis; NF B; TLR4

Indexed keywords

ASTRAGALIN; CYCLOOXYGENASE 2; ESCHERICHIA COLI LIPOPOLYSACCHARIDE; I KAPPA B ALPHA; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; INDUCIBLE NITRIC OXIDE SYNTHASE; INTERLEUKIN 6; MITOGEN ACTIVATED PROTEIN KINASE; MITOGEN ACTIVATED PROTEIN KINASE P38; NITRIC OXIDE; STRESS ACTIVATED PROTEIN KINASE; TOLL LIKE RECEPTOR 4; TUMOR NECROSIS FACTOR ALPHA; ANTIINFLAMMATORY AGENT; INTERLEUKIN-6, MOUSE; KAEMPFEROL DERIVATIVE; LIPOPOLYSACCHARIDE; LIPOPOLYSACCHARIDE A; NOS2 PROTEIN, MOUSE; PLANT MEDICINAL PRODUCT; PTGS2 PROTEIN, MOUSE; TLR4 PROTEIN, MOUSE;

ANIMAL CELL; ANTIINFLAMMATORY ACTIVITY; ARTICLE; BREAST EPITHELIUM; CELL VIABILITY; CONTROLLED STUDY; CYTOKINE RELEASE; DOSE RESPONSE; DRUG MECHANISM; ENZYME INACTIVATION; ENZYME LINKED IMMUNOSORBENT ASSAY; ENZYME PHOSPHORYLATION; FEMALE; MASTITIS; MOUSE; NONHUMAN; PERSIMMON; PRIMARY CELL CULTURE; PROTEIN DEGRADATION; PROTEIN EXPRESSION; SIGNAL TRANSDUCTION; WESTERN BLOTTING; ANIMAL; BAGG ALBINO MOUSE; CHEMICALLY INDUCED; CHEMISTRY; CYTOLOGY; DIOSPYROS; DRUG EFFECTS; DRUG INTERACTION; IMMUNOLOGY; METABOLISM; UDDER;

ANIMALS; ANTI-INFLAMMATORY AGENTS; CYCLOOXYGENASE 2; DIOSPYROS; DRUG INTERACTIONS; FEMALE; INTERLEUKIN-6; KAEMPFEROLS; LIPOPOLYSACCHARIDES; MAMMARY GLANDS, ANIMAL; MASTITIS; MICE, INBRED BALB C; NITRIC OXIDE; NITRIC OXIDE SYNTHASE TYPE II; PLANT PREPARATIONS; PRIMARY CELL CULTURE; SIGNAL TRANSDUCTION; TOLL-LIKE RECEPTOR 4; TUMOR NECROSIS FACTOR-ALPHA;

EID: 84912102490     PISSN: 00224804     EISSN: 10958673     Source Type: Journal    
DOI: 10.1016/j.jss.2014.05.059     Document Type: Article

References (37)

1. Zhao X, Lacasse P. Mammary tissue damage during bovine mastitis: causes and control. J Anim Sci 2008;86:57.
2. Yang W, Zerbe H, Petzl W, et al. Bovine TLR2 and TLR4 properly transduce signals from Staphylococcus aureus and E. coli, but S. aureus fails to both activate NF-kappaB in mammary epithelial cells and to quickly induce TNFalpha and interleukin-8 (CXCL8) expression in the udder. Mol Immunol 2008;45:1385.
3. De Schepper S, De Ketelaere A, Bannerman DD, Paape MJ, Peelman L, Burvenich C. The toll-like receptor-4 (TLR-4) pathway and its possible role in the pathogenesis of Escherichia coli mastitis in dairy cattle. Vet Res 2008;39:5.
4. Ibeagha-Awemu EM, Lee JW, Ibeagha AE, Bannerman DD, Paape MJ, Zhao X. Bacterial lipopolysaccharide induces increased expression of toll-like receptor (TLR) 4 and downstream TLR signaling molecules in bovine mammary epithelial cells. Vet Res 2008;39:11.
5. West AP, Koblansky AA, Ghosh S. Recognition and signaling by toll-like receptors. Annu Rev cell and developmental biology 2006;22:409.
6. Strandberg Y, Gray C, Vuocolo T, Donaldson L, Broadway M, Tellama R. Lipopolysaccharide and lipoteichoic acid induce different innate immune responses in bovine mammary epithelial cells. Cytokine 2005;31:72.
7. Lysakova-Devine T, Keogh B, Harrington B, et al. Viral inhibitory peptide of TLR4, a peptide derived from vaccinia protein A46, specifically inhibits TLR4 by directly targeting MyD88 adaptor-like and TRIF-related adaptor molecule. Journal of immunology 2010;185:4261.
8. Triantafilou M, Triantafilou K. The dynamics of LPS recognition: complex orchestration of multiple receptors. Journal of endotoxin research 2005;11:5.
9. Boulanger V, Bouchard L, Zhao X, Lacasse P. Induction of nitric oxide production by bovine mammary epithelial cells and blood leukocytes. Journal of dairy science 2001;84:1430.
10. Trakranrungsie N, Will J Expression of iNOS and COX-2 proteins during endotoxin-induced mastitis in guinea pigs. Faseb Journalfederation Amer Soc Exp Biol 9650 Rockville Pike, Bethesda, MD 20814-3998 USA, 1997:1829-1829.
11. Chen CC, Sun YT, Chen JJ, Chang YJ. Tumor necrosis factor-alpha-induced cyclooxygenase-2 expression via sequential activation of ceramide-dependent mitogen-activated protein kinases, and IkappaB kinase 1/2 in human alveolar epithelial cells. Molecular pharmacology 2001;59:493.
12. Burns K, Martinon F, Esslinger C, et al. MyD88, an adapter protein involved in interleukin-1 signaling. Journal of biological chemistry 1998;273:12203.
13. Rainard P, Riollet C. Innate immunity of the bovine mammary gland. Vet Res 2006;37:369.
14. Seegers H, Fourichon C, Beaudeau F. Production effects related to mastitis and mastitis economics in dairy cattle herds. Vet Res 2003;34:475.
15. Ke M, Hu XQ, Ouyang J, Dai B, Xu Y. The effect of astragalin on the VEGF production of cultured Muller cells under high glucose conditions. Bio-medical materials and engineering 2012;22:113.
16. Kim MS, Kim SH. Inhibitory effect of astragalin on expression of lipopolysaccharide-induced inflammatory mediators through NF-kappaB in macrophages. Archives of pharmacal research 2011;34:2101.
17. Soromou LW, Chen N, Jiang L, et al. Astragalin attenuates lipopolysaccharide-induced inflammatory responses by down-regulating NF-kappaB signaling pathway. Biochemical and biophysical research communications 2012;419:256.
18. Choi J, Kang HJ, Kim SZ, Kwon TO, Jeong SI, Jang SI. Antioxidant effect of astragalin isolated from the leaves of Morus alba L. against free radical-induced oxidative hemolysis of human red blood cells. Archives of pharmacal research 2013;36:912.
19. Li F, Liang D, Yang Z, et al. Astragalin suppresses inflammatory responses via down-regulation of NF-kappaB signaling pathway in lipopolysaccharide-induced mastitis in a murine model. International immunopharmacology 2013;17:478.
20. Mroue R, Bissell MJ. Three-dimensional cultures of mouse mammary epithelial cells. Epithelial cell culture protocols. Springer 2013;945:221-50.
21. Smalley MJ. Isolation, culture and analysis of mouse mammary epithelial cells. Methods in molecular biology 2010;633:139.
22. Gunther J, Koczan D, Yang W, et al. Assessment of the immune capacity of mammary epithelial cells: comparison with mammary tissue after challenge with Escherichia coli. Vet Res 2009;40:31.
23. Zhang J-M, An J. Cytokines, inflammation and pain. International anesthesiology clinics 2007;45:27.
24. Paape M, Mehrzad J, Zhao X, Detilleux J, Burvenich C. Defense of the bovine mammary gland by polymorphonuclear neutrophil leukocytes. Journal of mammary gland biology and neoplasia 2002;7:109.
25. Lahouassa H, Moussay E, Rainard P, Riollet C. Differential cytokine and chemokine responses of bovine mammary epithelial cells to Staphylococcus aureus and Escherichia coli. Cytokine 2007;38:12.
26. Miao JF, Zhu YM, Gu BB, Wang XB, Zou SX, Deng YE. Evaluation of the changes of immune cells during lipopolysaccharide-induced mastitis in rats. Cytokine 2007;40:135.
27. Kim J, Oh Y, Kim Y, Oh H, Cho Y. Polarized secretion of CXC chemokines by human intestinal epithelial cells in response to Bacteroides fragilis enterotoxin: NF-κB plays a major role in the regulation of IL-8 expression. Clinical & Experimental Immunology 2001;123:421.
28. Moreilhon C, Gras D, Hologne C, et al. Live Staphylococcus aureus and bacterial soluble factors induce different transcriptional responses in human airway cells. Physiological genomics 2005;20:244.
29. Kim M-S, Park S-B, Suk K, et al. Gallotannin isolated from Euphorbia Species, 1, 2, 6-Tri-O-galloyl-β-D-allose, decreases nitric oxide production through inhibition of nuclear factor-κB and downstream inducible nitric oxide synthase expression in macrophages. Biological and Pharmaceutical Bulletin 2009;32:1053.
30. Xie Q-W, Cho HJ. Cloning and characterization of inducible nitric oxide synthase from mouse macrophages. Science 1992;256:225.
31. Nagai H, Kumamoto H, Fukuda M, Takahashi T. Inducible nitric oxide synthase and apoptosis-related factors in the synovial tissues of temporomandibular joints with internal derangement and osteoarthritis. Journal of oral and maxillofacial surgery 2003;61:801.
32. Moncada S, Palmer RM, Higgs EA. Nitric oxide: physiology, pathophysiology, and pharmacology. Pharmacological reviews 1991;43:109.
33. Clancy RM, Amin AR, Abramson SB. The role of nitric oxide in inflammation and immunity. Arthritis & Rheumatism 1998;41:1141.
34. Belvisi MG, Saunders MA, Haddad EB, et al. Induction of cyclo-oxygenase-2 by cytokines in human cultured airway smooth muscle cells: novel inflammatory role of this cell type. British journal of pharmacology 1997;120:910.
35. Gilbert FB, Cunha P, Jensen K, et al. Differential response of bovine mammary epithelial cells to Staphylococcus aureus or Escherichia coli agonists of the innate immune system. Vet Res 2013;44:40.
36. Li D, Fu Y, Zhang W, et al. Salidroside attenuates inflammatory responses by suppressing nuclear factor-κB and mitogen activated protein kinases activation in lipopolysaccharide-induced mastitis in mice. Inflammation Research 2013;62:9.
37. Liang D, Li F, Fu Y, et al. Thymol inhibits LPS-stimulated inflammatory response via down-regulation of NF-kappaB and MAPK signaling pathways in mouse mammary epithelial cells. Inflammation 2013;37:214.