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Chungyangeum Attenuated the Allergic Inflammation in vivo and in vitro  

Kim, Su-Jin (Department of Cosmeceutical Science, Daegu Hanny University)
Lee, Jae-Ho (Department of Herbal Medicinal Pharmacology, Daegu Haany University)
Oh, Chung Hwan (Department of Herbal Medicinal Pharmacology, Daegu Haany University)
Oh, Sa-Rang (College of Pharmacy, Keimyung University)
Jung, Ji-Wook (Department of Herbal Medicinal Pharmacology, Daegu Haany University)
Abstract
Chungyangeum (CYE) is a newly designed herbal drug formula for the purpose of treating atopic dermatitis. The aim of the present study is to elucidate whether and how CYE modulates the allergy inflammation in vitro and in vivo. We investigate to ascertain the pharmacological effects of CYE on both compound 48/80 or histamine-induced scratching behaviors and 2, 4-dinitrochlrobenzene (DNCB)-induced atopic dermatitis in mice. Additionally, we attempted to determine the effects of CYE on lipopolysaccharide (LPS)-induced inflammatory responses in macrophages. The findings of this study demonstrated that CYE reduced compound 48/80 or histamine-induced scratching behaviors and DNCB-induced atopic dermatitis in mice. The CYE inhibited the production of inflammatory cytokines as well as the activation of NF-${\kappa}B$ and caspase-1 in stimulated macrophages. Collectively, the findings of this study provide us with novel insights into the pharmacological actions of CYE as a potential molecule for use in the treatment of allergic inflammation diseases.
Keywords
Chungyangeum; Inflammatory mediators; Allergic inflammation; Nuclear factor-${\kappa}B$; Caspase-1;
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1 Trefzer U, Hofmann M, Sterry W, Asadullah K. Cytokine and anticytokine therapy in dermatology. Expert Opin Biol Ther. 2003. 3: 733-743.   DOI   ScienceOn
2 Wang X, Wang H, Figueroa BE, Zhang WH, Huo C, Guan Y, Zhang Y, Bruey JM, Reed JC, Friedlander RM. Dysregulation of receptor interacting protein-2 and caspase recruitmentdomain only protein mediates aberrant caspase-1 activation in Huntington's disease. J Neurosci. 2005. 25: 11645-11654.   DOI   ScienceOn
3 Allam JP, Novak N. The pathophysiology of atopic eczema. Clin Exp Dermatol. 2006. 31: 89-93.   DOI   ScienceOn
4 Bauernfeind FG, Horvath G, Stutz A, Alnemri ES, MacDonald K, Speert D, Fernandes-Alnemri T, Wu J, Monks BG, Fitzgerald KA, Hornung V, Latz E. Cutting edge: NF-kappaB activating pattern recognition and cytokine receptors license NLRP3 inflammasome activation by regulating NLRP3 expression. J Immunol. 2009. 183: 787-791.   DOI   ScienceOn
5 Boero S, Silvestri M, Ullmann N, Rossi GA. Modulation by flunisolide of tumor necrosis factor-alpha-induced stimulation of airway epithelial cell activities related to eosinophil inflammation. J Asthma. 2010. 47: 381-387.   DOI   ScienceOn
6 Brenninkmeijer EE, Spuls PI, Legierse CM, Lindeboom R, Smitt JH, Bos JD. Clinical differences between atopic and atopiform dermatitis. J Am Acad Dermatol. 2008. 58: 407-414.   DOI   ScienceOn
7 Buske-Kirschbaum A, Geiben A, Hellhammer D. Psychobiological aspects of atopic dermatitis: an overview. Psychother Psychosom. 2001. 70: 6-16.   DOI   ScienceOn
8 Druilhe A, Srinivasula SM, Razmara M, Ahmad M, Alnemri ES. Regulation of IL-1beta generation by Pseudo-ICE and ICEBERG, two dominant negative caspase recruitment domain proteins. Cell Death Differ. 2001. 8: 649-657.   DOI   ScienceOn
9 Gadaleta RM, Oldenburg B, Willemsen EC, Spit M, Murzilli S, Salvatore L, Klomp LW, Siersema PD, van Erpecum KJ, van Mil SW. Activation of bile salt nuclear receptor FXR is repressed by pro-inflammatory cytokines activating NF-_{\kappa}B signaling in the intestine. Biochim Biophys Acta. 2011. 1812: 851-858.   DOI   ScienceOn
10 Gilmore TD, Garbati MR. Inhibition of NF-${\kappa}B$ signaling as a strategy in disease therapy. Curr Top Microbiol Immunol. 2011. 349: 245-263.
11 Leung DY, Bieber T. Atopic dermatitis. Lancet. 2003. 361: 151-160.   DOI   ScienceOn
12 Tegeder I, Pfeilschifter J, Geisslinger G. Cyclooxygenaseindependent actions of cyclooxygenase inhibitors. FASEB J. 2001. 15: 2057-2072.   DOI   ScienceOn
13 Gold MS, Kemp AS. Atopic disease in childhood. Med J Aust. 2005. 182: 298-304.
14 Humke EW, Shriver SK, Starovasnik MA, Fairbrother WJ, Dixit VM. ICEBERG: a novel inhibitor of interleukin-1beta generation. Cell. 2000. 103: 99-111.   DOI   ScienceOn
15 Kim SJ, Chung WS, Kim SS, Ko SG, Um JY. Antiinflammatory effect of Oldenlandia diffusa and its constituent, hentriacontane, through suppression of caspase-1 activation in mouse peritoneal macrophages. Phytother Res. 2011. 25: 1537-1546.   DOI   ScienceOn
16 Lee SH, Stehlik C, Reed JC. Cop, a caspase recruitment domaincontaining protein and inhibitor of caspase-1 activation processing. J Biol Chem. 2001. 276: 34495-34500.   DOI   ScienceOn
17 McCormick TS, Stevens SR, Kang K. Macrophages and cutaneous inflammation. Nat Biotechnol. 2000. 18: 25-26.   DOI   ScienceOn
18 Minami K, Kamei C. A chronic model for evaluating the itching associated with allergic conjunctivitis in rats. Int Immunopharmacol. 2004. 4: 101-108.   DOI   ScienceOn
19 Mukaida N. Interleukin-8: an expanding universe beyond neutrophil chemotaxis and activation. Int J Hematol. 2000. 72: 391-398.
20 Shiohara T, Hayakawa J, Mizukawa Y. Animal models for atopic dermatitis: are they relevant to human disease? J Dermatol Sci. 2004. 36: 1-9.   DOI   ScienceOn
21 Faubel S, Lewis EC, Reznikov L, Ljubanovic D, Hoke TS, Somerset H, Oh DJ, Lu L, Klein CL, Dinarello CA, Edelstein CL. Cisplatin-induced acute renal failure is associated with an increase in the cytokines interleukin (IL)-1beta, IL-18, IL-6, and neutrophil infiltration in the kidney. J Pharmacol Exp Ther. 2007. 322: 8-15.   DOI   ScienceOn
22 Taxman DJ, Holley-Guthrie EA, Huang MT, Moore CB, Bergstralh DT, Allen IC, Lei Y, Gris D, Ting JP. The NLR adaptor ASC/ PYCARD regulates DUSP10, mitogen-activated protein kinase (MAPK), and chemokine induction independent of the inflammasome. J Biol Chem. 2011. 286: 19605-19616.   DOI   ScienceOn