Synergic Anti-Pruritic and Anti-Inflammatory Effects of Scutellariae Radix plus Flos Loncerae Extracts in Rat Peritoneal Mast Cell and Chemical Antigen-Induced Mice

렛트 복강 비만세포와 화학항원 유도 알레르기 마우스에서 황금과 금은화 추출물의 항가려움 및 항염증 상승효과

  • Received : 2013.01.21
  • Accepted : 2013.02.14
  • Published : 2013.02.25

Abstract

Pruritus is a unpleasant symptom in the skin that provokes the act of or desire to scratch. Mast cells are important effector cells in allergic reactions such as pruritus and inflammation. The purpose of this study was undertaken to investigate the synergic anti-pruritic and anti-inflammatory effects of Scutellariae Radix (SB) plus Flos Loncerae (FL) extracts in rat peritoneal mast cells (RPMCs), pruritogen-induced scratching mice and 2,4-dinitrofluorobenzene (DNFB)-induced allergic mice. We investigated the effect of SB, FL and SB plus FL extracts on the production of tumor necrosis factor (TNF)-${\alpha}$, interleukin (IL)-$1{\beta}$, and histamine in RPMCs, on the scratching behavior in ICR mice, and skin clinical serverity and inflammatory mediators in DNFB-induced allergic hairless mice. RPMCs stimulated with PMA plus A23187 or compound 48/80 significantly increased TNF-${\alpha}$, IL-$1{\beta}$ or histamine production compared with media control. However, TNF-${\alpha}$ IL-$1{\beta}$ or histamine levels increased by PMA plus A23187 or compound 48/80 treatment were significantly inhibited by SB, FL in a dose-dependent manner. Especially, SB plus FL pretreatment had a synergic inhibitory effects on stimulator-induced cytokines (TNF-${\alpha}$ and IL-$1{\beta}$) and histamine production. Moreover, SB plus FL administration had a synergic inhibitory effects on the scratching behavior induced by pruritogen (compound 48/80, histamine, serotonin, substance P) in ICR mice. Furthermore, SB plus FL administration had a synergic inhibitory effects on skin damage, inflammatory mediators, leukocyte and mast cell infiltration induced by DNFB in hairless mice. These results suggest that SB plus FL administration has a potential use as a medicinal plant for treatment against itching and inflammation-related skin disease.

Keywords

References

  1. Metz, M., Grundmann, S., Stander, S. Pruritus: an overview of current concepts. Vet Dermatol. 22: 121-131, 2011. https://doi.org/10.1111/j.1365-3164.2010.00945.x
  2. Pfaar, O., Raap, U., Holz, M., Hormann, K., Klimek, L. Pathophysiology of itching and sneezing in allergic rhinitis. Swiss Med Wkly. 139: 35-40, 2009.
  3. Casset, A., Braun, J.J. Relationships between indoor allergens, sensitization, and allergic asthma and rhinitis symptoms. Rev Mal Respir. 27: 913-920, 2010. https://doi.org/10.1016/j.rmr.2010.07.006
  4. Kimber, I., Basketter, D.A., Gerberick, G.F., Ryan, C.A., Dearman, R.J. Chemical allergy: translating biology into hazard characterization. Toxicol Sci. 120 Suppl 1: S238-268, 2012.
  5. O'Neill, J.L., Chan, Y.H., Rapp, S.R., Yosipovitch, G. Differences in itch characteristics between psoriasis and atopic dermatitis patients: results of a web-based questionnaire. Acta Derm Venereol. 91: 537-540, 2011. https://doi.org/10.2340/00015555-1126
  6. Kamo, A., Tominaga, M., Tengara, S., Ogawa, H., Takamori, K. Inhibitory effects of UV-based therapy on dry skin-inducible nerve growth in acetone-treated mice. J Dermatol Sci. 62: 91-97, 2011. https://doi.org/10.1016/j.jdermsci.2011.01.004
  7. Shin, J.W., Jin, S.P., Lee, J.H., Cho, S. Analysis of MAST-CLA Results as a Diagnostic Tool in Allergic Skin Diseases. Ann Dermatol. 22: 35-40, 2010. https://doi.org/10.5021/ad.2010.22.1.35
  8. Kay, A.B. Overview of allergy and allergic diseases: with a view to the future. Br Med Bull. 56: 843-864, 2000. https://doi.org/10.1258/0007142001903481
  9. Casset, A., Braun, J.J. Relationships between indoor allergens, sensitization, and allergic asthma and rhinitis symptoms]. Rev Mal Respir. 27: 913-920, 2010. https://doi.org/10.1016/j.rmr.2010.07.006
  10. Spergel J.M. Epidemiology of atopic dermatitis and atopic march in children. Immunol Allergy Clin North Am. 30: 269-280, 2010. https://doi.org/10.1016/j.iac.2010.06.003
  11. Spergel, J.M., Paller, A.S. Atopic dermatitis and the atopic march. J Allergy Clin Immunol. 112(6 Suppl):S118-127, 2003. https://doi.org/10.1016/j.jaci.2003.09.033
  12. Lasic, D., Cvitanovic, M.Z., Uglesic, B., Visic, V., Hlevnjak, I. Exanthema medicamentosum as a side effect of promazine. Psychiatr Danub. 23: 194-197, 2011.
  13. Zhou, X.Q., Liang, H., Lu, X.H., Cai, S.Q., Wang, B., Zhao, Y.Y. Flavonoids from Scutellaria baicalensis and their bioactivities]. Beijing Da Xue Xue Bao. 41: 578-584, 2009.
  14. Trinh, H.T., Joh, E.H., Kwak, H.Y., Baek, N.I., Kim, D.H. Anti-pruritic effect of baicalin and its metabolites, baicalein and oroxylin A, in mice. Acta Pharmacol Sin. 31: 718-724, 2010. https://doi.org/10.1038/aps.2010.42
  15. Kim, E.H., Shim, B., Kang, S., Jeong, G., Lee, J.S., Yu, Y.B., Chun, M. Anti-inflammatory effects of Scutellaria baicalensis extract via suppression of immune modulators and MAP kinase signaling molecules. J Ethnopharmacol. 126: 320-331, 2009. https://doi.org/10.1016/j.jep.2009.08.027
  16. Kumagai, T., Muller, C.I., Desmond, J.C., Imai, Y., Heber, D., Koeffler, H.P. Scutellaria baicalensis, a herbal medicine: anti-proliferative and apoptotic activity against acute lymphocytic leukemia, lymphoma and myeloma cell lines. Leuk Res. 31: 523-530, 2007. https://doi.org/10.1016/j.leukres.2006.08.019
  17. Lee, B.S., Shim, S.M., Heo, J., Pae, H.O., Seo, B.Y., Han, S.Y., Sohn, D.H., Jang, S.I., Chung, H.T. Wogonin suppresses TARC expression induced by mite antigen via heme oxygenase 1 in human keratinocytes. Suppressive effect of wogonin on mite antigen-induced TARC expression. J Dermatol Sci. 46: 31-40, 2007. https://doi.org/10.1016/j.jdermsci.2007.01.001
  18. Mehendale, S., Aung, H., Wang, C.Z., Tong, R., Foo, A., Xie, J.T., Yuan, C.S. Scutellaria baicalensis and a constituent flavonoid, baicalein, attenuate ritonavir-induced gastrointestinal side-effects. J Pharm Pharmacol. 59: 1567-1572, 2007. https://doi.org/10.1211/jpp.59.11.0015
  19. Kumar, N., Singh, B., Bhandari, P., Gupta, A.P., Uniyal, S.K., Kaul, V.K. Biflavonoids from Lonicera japonica. Phytochemistry. 66: 2740-2744, 2005. https://doi.org/10.1016/j.phytochem.2005.10.002
  20. Oku, H., Ogawa, Y., Iwaoka, E., Ishiguro, K. Allergypreventive effects of chlorogenic acid and iridoid derivatives from flower buds of Lonicera japonica. Biol Pharm Bull. 34: 1330-1333, 2011. https://doi.org/10.1248/bpb.34.1330
  21. Kwak, W.J., Han, C.K., Chang, H.W., Kim, H.P., Kang, S.S., Son, K.H. Loniceroside C, an antiinflammatory saponin from Lonicera japonica. Chem Pharm Bull (Tokyo). 51: 333-335, 2003. https://doi.org/10.1248/cpb.51.333
  22. Park, H.S., Park, K.I., Lee, D.H., Kang, S.R., Nagappan, A., Kim, J.A., Kim, E.H., Lee, W.S., Shin, S.C., Hah, Y.S., Kim, G.S. Polyphenolic extract isolated from Korean Lonicera japonica Thunb. induce G2/M cell cycle arrest and apoptosis in HepG2 cells: involvements of PI3K/Akt and MAPKs. Food Chem Toxicol. 50: 2407-2416, 2012. https://doi.org/10.1016/j.fct.2012.04.034
  23. Chan, B.C., Hon, K.L., Leung, P.C., Sam, S.W., Fung, K.P., Lee, M.Y., Lau, H.Y. Traditional Chinese medicine for atopic eczema: PentaHerbs formula suppresses inflammatory mediators release from mast cells. J Ethnopharmacol. 120: 85-91, 2008. https://doi.org/10.1016/j.jep.2008.07.034
  24. 황치환, 윤채성, 송승현, 원영호, 황충연. 갈근해기탕가미방(葛根解肌湯加味方)과 삼황세제가미방(三黃洗劑加味方) 병용이 NC/Nga 생쥐의 아토피 피부염에 미치는 영향. 대한외관과학회지 21: 1-18, 2008.
  25. 허정훈, 송한나, 장선일. rSj26 또는 화학 항원 유도 아토피 피부염 마우스 모델에서 가감보중익기탕의 면역 매개물 조절 및 상처치료 효과. 대한본초학회지 23: 53-61, 2008.
  26. Martynova, M.G., Bystrova, O.A., Moiseeva, O.M., Evdonin, A.L., Kondratov, K.A., Medvedeva, N.D. The presence of ANP in rat peritoneal mast cells. Cell Res. 15: 811-816, 2005. https://doi.org/10.1038/sj.cr.7290350
  27. Mihara, K., Kuratani, K., Matsui, T., Nakamura, M., Yokota, K. Vital role of the itch-scratch response in development of spontaneous dermatitis in NC/Nga mice. Br J Dermato. 151: 335-345, 2004. https://doi.org/10.1111/j.1365-2133.2004.06036.x
  28. Nakae, S., Suto, H., Kakurai, M., Sedgwick, J.D., Tsai, M., Galli, S.J. Mast cells enhance T cell activation: importance of mast cell-derived TNF. Proc Natl Acad Sci USA. 102: 6467-6472, 2005. https://doi.org/10.1073/pnas.0501912102
  29. Galli, S.J. New concepts about the mast cell. N Engl J Med. 328: 257-265, 1993. https://doi.org/10.1056/NEJM199301283280408
  30. Mekori, Y.A., Metcalfe, D.D. Mast cells in innate immunity. Immunol Rev. 173: 131-140, 2000. https://doi.org/10.1034/j.1600-065X.2000.917305.x
  31. Hosoda, M., Yamaya, M., Suzuki, T., Yamada, N., Kamanakam, M., Sekizawa, K., Butterfield, J.H., Watanabe, T., Nishimura, H., Sasaki, H. Effects of rhinovirus infection on histamine and cytokine production by cell lines from human mast cells and basophils. J Immunol. 169:1482-1491, 2002. https://doi.org/10.4049/jimmunol.169.3.1482
  32. Takai, T., Ikeda, S. Barrier dysfunction caused by environmental proteases in the pathogenesis of allergic diseases. Allergol Int. 60: 25-35, 2011. https://doi.org/10.2332/allergolint.10-RAI-0273
  33. Jung, H.S., Kim, M.H., Gwak, N.G., Im, Y.S., Lee, K.Y., Sohn, Y., Choi, H., Yang, W.M. Antiallergic effects of Scutellaria baicalensis on inflammation in vivo and in vitro. J Ethnopharmacol. 141: 345-349, 2012. https://doi.org/10.1016/j.jep.2012.02.044
  34. Benyon, R.C., Robinson, C., Church, M.K. Differential release of histamine and eicosanoids from human skin mast cells activated by IgE-dependent and non-immunological stimuli. Br J Pharmacol. 97: 898-904, 1989. https://doi.org/10.1111/j.1476-5381.1989.tb12030.x
  35. Takubo, M., Ueda, Y., Yatsuzuka, R., Jiang, S., Fujii, Y., Kamei, C. Characteristics of scratching behavior induced by some chemical mediators in hairless mice. J Pharmacol Sci. 100: 285-288, 2006. https://doi.org/10.1254/jphs.FPJ06002X