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The Effect of Extract from Sea Buckthorn on DNCB-induced Atopic Dermatitis in NC/Nga Mice

  • Park, Sang-Yong (Department of Oriental Medicinal Materials & Processing, Kyung Hee University) ;
  • Shin, Heon-Sub (Department of Oriental Medicinal Materials & Processing, Kyung Hee University) ;
  • Yang, Jung-Eun (Department of Oriental Medicinal Materials & Processing, Kyung Hee University) ;
  • Han, Sang-No (Samsung Herb Medicine Co., Ltd, Biotechnology Innovation Center) ;
  • Kim, Dae-Sung (Samsung Herb Medicine Co., Ltd, Biotechnology Innovation Center) ;
  • Kim, Myong-Jo (Department of Applied Plant Sciences, Oriental Bio-herb Research Institute, Gangwon National University) ;
  • Heo, Seong-Il (Department of Applied Plant Sciences, Oriental Bio-herb Research Institute, Gangwon National University) ;
  • Yi, Tae-Hoo (Department of Oriental Medicinal Materials & Processing, Kyung Hee University) ;
  • Lee, Jung-Min (Department of Oriental Medicinal Materials & Processing, Kyung Hee University)
  • Received : 2012.10.12
  • Accepted : 2012.12.17
  • Published : 2012.12.31

Abstract

Sea Buckthorn (Hippophae rhamnoides L.) has been used in traditional medicine for the treatment of cough, indigestion, circulatory problems and pain. The associated anti-inflammatory effect of this agent is achieved via the inhibition of Nf-${\kappa}B$ signaling, a property that has been demonstrated to effectively control the symptoms of various skin disorders, including atopic dermatitis. Accordingly, the purpose of this study was to assess the efficacy of Sea Buckthorn in reducing the production of lipopolysaccharide (LPS) activated nitric oxide (NO) by inhibiting the Nf-${\kappa}B$ pathway, as measured by the symptoms of atopic dermatitis (AD) occurring secondarily to inflammation and immune dysregulation. Our data demonstrate that Sea Buckthorn significantly decreased the LPS-induced production of NO (p<0.001). Atopic dermatitis was induced by repeated application of 2,4-dinitrochlorobenzene to the dorsal skin of mice. Topical application of 5% Sea Buckthorn extract improved the symptoms of AD, specifically reducing disease severity scores, scratching behaviors and epidermal thickness. When compared to the control group, animals treated with Sea Buckthorn exhibited increased serum IL-12 levels and decreased serum TNF-${\alpha}$, IL-4 and IL-5 levels. Such a modulation of biphasic T-helper (Th)1/Th2 cytokines may result in a reduction in serum IgE levels. Our findings suggest that mechanism of action of Sea Buckthorn in the treatment of AD is associated with a marked anti-inflammatory effect as well as an inhibition of Th2-mediated IgE overproduction via the modulation of biphasic Th1/Th2 cytokines. Such results suggest that topical Sea Buckthorn extract may prove to be a novel therapy for AD symptoms with few side effects.

Keywords

References

  1. Angelini, F., G. Di Matteo, S. Balestrero, E. Brunetti, G. Mancino, P. Rossi and E. Galli. 2007. Nuclear factor kappaB activity is increased in peripheral blood mononuclear cells of children affected by atopic and non-atopic eczema. Int. J. Immunopathol Pharmacol. 20(1):59-67.
  2. Anggard, E. 1994. Nitric oxide : mediator, murderer, and medicine. Lancet 343(8907):1199-1206. https://doi.org/10.1016/S0140-6736(94)92405-8
  3. Baeuerle, P.A. and D. Baltimore. 1996. NF-kB - Ten years after. Cell 87(1):13-20. https://doi.org/10.1016/S0092-8674(00)81318-5
  4. Baeuerle, P.A. 1998. IkB-NF-kB structure: at the interface of inflammation control. Cell 95(6):729-731. https://doi.org/10.1016/S0092-8674(00)81694-3
  5. Barnes, P.J. 2000. New direction in allergic: Mechanism-based anti-inflammatory therapies. J. Allergy Clin. Immunol. 106 (1):5-16. https://doi.org/10.1067/mai.2000.107930
  6. Chen, L., G. Lian and L. Han. 2008. Use of "bricks and mortar" model to predict transdermal permeation: model development and initial validation. Ind. Eng. Chem. Res. 47(17):6465- 6472. https://doi.org/10.1021/ie701711v
  7. Choi, J.H. 2000. Dyfunction skin barrier of atopic dermatitis. J. Asth. Allergy Chinical Immunol. 20(5):693-694.
  8. Ciebiada, M., M. Gorska and P. Gorski. 2011. SICAM-1 and TNF-a in asthma and rhinitis: relationship with the presence of atopy. J. Asthma. 48(7):660-666. https://doi.org/10.3109/02770903.2011.604886
  9. Coffman, R.L. and J.A. Carty. 1986. T cell activity that enhances polyclonal IgE production and its inhibition by interferon-gamma. J. Immunol. 136(3):949-954.
  10. D'Acquisto, F., T. Iuvone, L. Rombola L. Sautebin, M. Di Rosa and R. Carnuccio. 1997. Involvement of NF-kappaB in the regulation of cyclooxygenase-2 protein expression in LPS-stimulated J774 macrophages. FEBS Lett. 418(1):175- 178. https://doi.org/10.1016/S0014-5793(97)01377-X
  11. Darsow, U., A. Wollenberg, D. Simon, A. Taieb, T. Werfel, A. Oranje, C. Gelmetti, A. Svensson, M. Deleuran, A.M. Calza, F. Giusti, J. Lubbe, S. Seidenari and J. Ring. 2010. ETFAD/EADV eczema task force 2009 position paper on diagnosis and treatment of atopic dermatitis. J. Eur. Acad. Dermatol. Venereol. 24(3):317-328. https://doi.org/10.1111/j.1468-3083.2009.03415.x
  12. Eccleston, C., Y. Baoru, R. Tahvonen, H. Kallio, G.H. Rimbach and A.M. Minihane. 2002. Effect of an antioxidant rich juice (sea buckthorn) on risk factors for coronary heart disease in humans. J. Nutr. Biochem. 13(6):346-354. https://doi.org/10.1016/S0955-2863(02)00179-1
  13. Ganju, L., Y. Padwad, R. Singh, D. Karan, S. Chanda, M.K. Chopra, P. Bhatnagar, R. Kashyap and R.C. Sawhney. 2005. Anti-inflammatory activity of seabuckthorn (Hippophae rhamnoides L.) leaves. Int. Immunopharmacol. 5(12):1675- 1684. https://doi.org/10.1016/j.intimp.2005.03.017
  14. Geetha, S., R.M. Sai, S.S. Mongia, V. Singj, G. Havazhagan and R.C. Sawhney. 2003. Evaluation of antioxidant activity of leaf extract of sea buckthorn (Hippophae rhamnoides L.) on chromium (VI) induced oxidative stress in albino rats. J. Ethnopharmacol. 87(2-3):247-251. https://doi.org/10.1016/S0378-8741(03)00154-5
  15. Goel, H.C., J. Prasad, S. Singh, R.K. Sagar, I.P. Kumar and A.K. Sinha. 2002. Radioprotection by a herbal preparation of Hippophae rhamnoides, RH-3 against whole body lethal irradiation in mice. Phytomedicine 9(1):15-25. https://doi.org/10.1078/0944-7113-00077
  16. Horiuchi, Y., S. Bae, I. Katayama and K. Nishioka. 2004. Therapeutic effects of streptococcal preparation OK-432 on atopic dermatitis-like lesions in NC/Nga mice: possible shift from a Th2- to Th1- predominance. J. Dermatol. Sci. 35(3): 187-197. https://doi.org/10.1016/j.jdermsci.2004.06.006
  17. Hunnum, Y.A. and R.M. Bell. 1989. Function of sphingolipid breakdown production in cellular regulation. Science 243: 500-507. https://doi.org/10.1126/science.2643164
  18. Inagaki, N., K. Igeta, J.F. Kim, M. Nagao, N. Shiraishi and N. Nakamura. 2002. Involvement of unique mechanisms in the induction of scratching behavior in BALB/c mice by compound 48/80. Eur. J. Pharmacol. 448(2-3):175-183. https://doi.org/10.1016/S0014-2999(02)01933-7
  19. Inagaki, N., K. Igeta, N. Shiraishi, J.F. Kim, M. Nagao, N. Nakamura and H. Nagai. 2003. Evaluation and characterization of mouse scratching behavior by a new apparatus, MicroAct. Skin Pharmacol. Appl. Skin Physiol. 16(3):165- 175. https://doi.org/10.1159/000069755
  20. Kawakami, T., T. Ando, M. Kimura, B.S. Wilson and Y. Kawakami. 2009. Mast cells in atopic dermatitis. Curr. Opin. Immunol. 21(6):666-678. https://doi.org/10.1016/j.coi.2009.09.006
  21. Kenichiro, T., A. Tsugunobu, U. Haruna, L. JungBum and K. Yasushi. 2009. Involvement of tryptase and proteinaseactivated receptor-2 in spontaneous itch-associated response in mice with atopy-like dermatitis. J. Pharmacol. Sci. 109(3):388-395. https://doi.org/10.1254/jphs.08332FP
  22. Kim, Y.J., S.C. Kang, S. Namkoong, M.G. Choung and E.H. Sohn. 2012. Anti-inflammatory effects by Arctium lappa L. root extracts through the regulation of ICAM-1 and nitric oxide. Korean J. Plant Res. 25(1):1-6 (in Korean). https://doi.org/10.7732/kjpr.2012.25.1.001
  23. Ko, M.J., S.Y. Park, K.J. Lee, T.H. Yi, W.C. Lee, C.K. Han and J.H. Khil. 2010. Anti-inflammatory effects of Pharbitis nil choisy in lipopolysaccharide-induceds RAW 264.7 cells. J. Beauty Trichol. 6(2):105-111 (in Korean).
  24. Lee, E.J., G.E. Ji and M.K. Sung. 2010. Quercetin and kaempferol suppress immunoglobulin E-mediated allergic inflammation in RBL-2H3 and Caco-2 cells. Inflamm. Res. 59(10):847-854. https://doi.org/10.1007/s00011-010-0196-2
  25. Lee, S.H., S.M. Hwang, W.H. Choi and S.G. Ahn. 1999. Skin barrier. Kor. J. Dermatol. 37(7):825-837 (in Korean).
  26. Li, Y.X., N. Li, Y.S. Li, B. Wu and J.S. Li. 2000. Upregulated intragraft gene expression, ICAM-1 and IL-2R molecules, and apoptotic epithelial cells during regection of rat small intestine allgrafts. Transplant Proceed. 32(6):1283-1286. https://doi.org/10.1016/S0041-1345(00)01227-6
  27. Maheshwari, D.T., M.S. Yogendra, S.K. Verma, V.K. Singh and S.N. Singh. 2011. Antioxidant and hepatoprotective activities of phenolic rich fraction of Seabuckthorn (Hippophae rhamnoides L.) leaves. Food Chem. Toxicol. 49(9):2422-2428. https://doi.org/10.1016/j.fct.2011.06.061
  28. Merja, H., P. Jytki and J.T. Riitta. 2006. Effects of different organic farming methods on the concentration of phenolic compounds in sea buckthorn leaves. J. Argic. Food Chem. 54(20):7678-7685. https://doi.org/10.1021/jf061018h
  29. Morise, Z., S. Komatsu, J.W. Fuseler, D.N. Granger, M. Perry, A.C. Issekutz and M.B. Grisham. 1998. ICAM-1 and P-selectin expression in a model of NSAID-induced gastropathy. Am. J. Physio. 274(2):246-252.
  30. Nakagami, H., N. Tomita, Y. Kaneda, T. Ogihara and R. Morishita. 2006. Anti-oxidant gene therapy by NF kappa B decoy oligodeoxynucleotide. Curr. Pharm. Biotechnol. 7(2):95-100. https://doi.org/10.2174/138920106776597702
  31. Namkoong, S., H.M. Joo, S.A. Jang, Y.J. Kim, T.S. Kim and E.H. Sohn. 2012. Suppressive Effects of Fucoxanthin on Degranulation in IgE-antigen complex-stimulated RBL-2H3 Cells. Korean J. Plant Res. 25(3):339-345. https://doi.org/10.7732/kjpr.2012.25.3.339
  32. Novak, N. 2009. New insights into the mechanism and management of allergic diseases: atopic dermatitis. Allergy 64(2):265-275. https://doi.org/10.1111/j.1398-9995.2008.01922.x
  33. Numerof, R.P. and K. Asadullah. 2006. Cytokine and anticytokine therapies for psoriasis and atopic dermatitis. BioDrugs 20(2):93-103. https://doi.org/10.2165/00063030-200620020-00004
  34. Park, B.D. and S.H. Lee. 2000. Atopic dermatitis and ceramide. J. Skin Bar. Res. 2(1):27-35 (in Korean).
  35. Park, H.N., W.H. Choi, K.G. Lee, S.P. Hong, S.H. Lee and S.G. Ahn. 2005. The effects of testosterone on skin barrier. Kor. J. Dermatol. 43(2):167-176 (in Korean).
  36. Park, M.S., B.S. Chang and D.H. Kim. 2011. The bathing effect of mineral-rich water on atopic dermatitis like skin lesions in hairless mice. J. Beauty Trichol. 7(2):181- 187 (in Korean).
  37. Pate, M.B., J.K. Smith, D.S. Chi and G. Krishnaswamy. 2010. Regulation and dysregulation of immunoglobulin E: a molecular and clinical perspective. Clin. Mol. Allergy. 8(3):1-13. https://doi.org/10.1186/1476-7961-8-1
  38. Reinhold, U., G. Pawelec, W. Wehrmann, M. Herold, P. Wernet and H.W. Kreysel. 1988. Immunoglobulin E and immunoglobulin G subclass distribution in vivo and relationship to in vitro generation of interferon-gamma and neopterin in patients with severe atopic dermatitis. Int. Arch. Allergy Appl. Immunol. 87(2):120-126. https://doi.org/10.1159/000234661
  39. Richard, T.B. and E.S. Paul. 2008. Hippophae rhamnoides L. common seabuckthorn. In The Woody Plant Seed Manual, Forest service, USA. pp. 588-589.
  40. Robert, J.B., C. Michael, R. Klaus, E.S. Karin, O.A. Hans, G. Bengt, H. Henrik and M. Mads. 2009. Immunoglobulin subclass levels in patients with non-Hodgkin lymphoma. Int. J. Cancer. 124(11):2616-2620. https://doi.org/10.1002/ijc.24245
  41. Rousi, A. 1971. The genus Hippophae L.: A taxonomic study. Ann. Bot. Fenn. 8(2):177-227.
  42. Suleyman, H., L.O. Demirezer, M.E. Buyukokuroglu, M.F. Akcay, A. Gepdiremen, Z.N. Banoglu and F. Gocer. 2001. Antiulcerogenic effect of Hippophae rhamnoides L. Phytother. Res. 15(7):625-627. https://doi.org/10.1002/ptr.831
  43. Suleyman, H., K. Gumustekin, S. Taysi, S. Keles, N. Oztasan, O. Aksas, K. Altinkaynak, H. Timur, F. Akcay, S. Akar, S. Dane and M. Gul. 2002. Beneficial effects of Hippophae rhamnoides L. on nicotine induced oxidative stress in rat blood compared with vitamin E. Biol. Pharm. Bull. 25(9): 1133-1136. https://doi.org/10.1248/bpb.25.1133
  44. Suzuki, Y., T. Yoshimaru, T. Matsui, T. Inoue, O. Niide, S. Nunomura and C. Ra. 2003. $Fc \varepsilon RI$signaling of mast cells activates intracellular production of hydrogen peroxide: Role in the regulation of calcium signals. J. Immunol. 171(11):6119-6127. https://doi.org/10.4049/jimmunol.171.11.6119
  45. Vichyanond, P. 2011. Omalizumab in allergic diseases, a recent review. Asian Pac. J. Allergy Immunol. 29(3):209-219.