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Anti-inflammatory effect of aged black garlic on 12-O-tetradecanoylphorbol-13-acetate-induced dermatitis in mice

  • You, Bo Ram (Department of Food and Nutrition, Chungnam National University) ;
  • Yoo, Jae-Myung (Korean Medicine-Application Center, Korea Institute of Oriental Medicine) ;
  • Baek, Seong Yeon (Department of Food and Nutrition, Chungnam National University) ;
  • Kim, Mee Ree (Department of Food and Nutrition, Chungnam National University)
  • Received : 2018.07.16
  • Accepted : 2019.02.12
  • Published : 2019.06.01

Abstract

BACKGROUND/OBJECTIVES: Although aged black garlic has various biological activities such as anti-allergy, anti-inflammation and neuroprotection, effect of aged black garlic on chemically contact dermatitis is unclarified. MATERIALS/METHODS: To evaluate anti-dermatitic activity of aged black garlic extract, we investigated effects of a fraction of aged black garlic extract (BG10) on both in vivo and in vitro. RESULTS: BG10 almost inhibited formation of nitric monoxide and interleukin-6 (IL-6; $IC_{50}$, $7.07{\mu}g/mL$) at $25{\mu}g/mL$, and dose-dependently reduced production of tumor necrosis $factor-{\alpha}$ ($TNF-{\alpha}$; $IC_{50}$, $52.07{\mu}g/mL$) and prostaglandin $E_2$ ($IC_{50}$, $38.46{\mu}g/mL$) in lipopolysaccharide-stimulated RAW264.7 cells. In addition, BG10 significantly inhibited the expression of inducible nitric oxide synthase, cyclooxygenase-2 and nuclear $NF-{\kappa}B$, and improved that of cytosolic levels of $NF-{\kappa}B$ and $I{\kappa}B{\alpha}$ in the cells. Consistent with in vitro studies, BG10 (0.5 mg/mL) not only reduced ear edema but also suppressed the formation of IL-6 and $TNF-{\alpha}$ induced by 12-O-tetradecanoylphorbol-13-acetate in ear tissues of mice. CONCLUSIONS: These findings suggest BG10 has anti-dermatitic activity through inhibiting activation of macrophages. Therefore, such effects of BG10 may provide information for the application of aged black garlic for prevention and therapy of contact dermatitis.

Keywords

References

  1. Dhingra N, Gulati N, Guttman-Yassky E. Mechanisms of contact sensitization offer insights into the role of barrier defects vs. intrinsic immune abnormalities as drivers of atopic dermatitis. J Invest Dermatol 2013;133:2311-4. https://doi.org/10.1038/jid.2013.239
  2. Perez-Pimiento AJ, Santaolalla M, de Paz S, Fernandez-Parra B, Dominguez-Lazaro AR, Moneo I. Anaphylactic reaction to young garlic. Allergy 1999;54:626-9. https://doi.org/10.1034/j.1398-9995.1999.00806.x
  3. Itoh T, Ohguchi K, Iinuma M, Nozawa Y, Akao Y. Inhibitory effect of xanthones isolated from the pericarp of Garcinia mangostana L. on rat basophilic leukemia RBL-2H3 cell degranulation. Bioorg Med Chem 2008;16:4500-8. https://doi.org/10.1016/j.bmc.2008.02.054
  4. Gilfillan AM, Tkaczyk C. Integrated signalling pathways for mast-cell activation. Nat Rev Immunol 2006;6:218-30. https://doi.org/10.1038/nri1782
  5. Butt MS, Sultan MT, Butt MS, Iqbal J. Garlic: nature's protection against physiological threats. Crit Rev Food Sci Nutr 2009;49:538-51. https://doi.org/10.1080/10408390802145344
  6. Liu CT, Sheen LY, Lii CK. Does garlic have a role as an antidiabetic agent? Mol Nutr Food Res 2007;51:1353-64. https://doi.org/10.1002/mnfr.200700082
  7. Thomson M, Ali M. Garlic [Allium sativum]: a review of its potential use as an anti-cancer agent. Curr Cancer Drug Targets 2003;3:67-81. https://doi.org/10.2174/1568009033333736
  8. Amagase H, Petesch BL, Matsuura H, Kasuga S, Itakura Y. Intake of garlic and its bioactive components. J Nutr 2001;131:955S-62S. https://doi.org/10.1093/jn/131.3.955S
  9. Lanzotti V. The analysis of onion and garlic. J Chromatogr A 2006;1112:3-22. https://doi.org/10.1016/j.chroma.2005.12.016
  10. Borrelli F, Capasso R, Izzo AA. Garlic (Allium sativum L.): adverse effects and drug interactions in humans. Mol Nutr Food Res 2007;51:1386-97. https://doi.org/10.1002/mnfr.200700072
  11. Burden AD, Wilkinson SM, Beck MH, Chalmers RJ. Garlic-induced systemic contact dermatitis. Contact Dermatitis 1994;30:299-300. https://doi.org/10.1111/j.1600-0536.1994.tb00603.x
  12. Moriguchi T, Saito H, Nishiyama N. Anti-ageing effect of aged garlic extract in the inbred brain atrophy mouse model. Clin Exp Pharmacol Physiol 1997;24:235-42. https://doi.org/10.1111/j.1440-1681.1997.tb01813.x
  13. Banerjee SK, Mukherjee PK, Maulik SK. Garlic as an antioxidant: the good, the bad and the ugly. Phytother Res 2003;17:97-106. https://doi.org/10.1002/ptr.1281
  14. Bae SH, Lee SW, Kim MR, Kim JM, Suh HJ. Influence of steeping solution and storage temperature on the color change of garlic. J Food Sci 2010;75:C108-12. https://doi.org/10.1111/j.1750-3841.2009.01439.x
  15. Imai J, Ide N, Nagae S, Moriguchi T, Matsuura H, Itakura Y. Antioxidant and radical scavenging effects of aged garlic extract and its constituents. Planta Med 1994;60:417-20. https://doi.org/10.1055/s-2006-959522
  16. Yoo JM, Sok DE, Kim MR. Anti-allergic action of aged black garlic extract in RBL-2H3 cells and passive cutaneous anaphylaxis reaction in mice. J Med Food 2014;17:92-102. https://doi.org/10.1089/jmf.2013.2927
  17. Kim MJ, Yoo YC, Kim HJ, Shin SK, Sohn EJ, Min AY, Sung NY, Kim MR. Aged black garlic exerts anti-inflammatory effects by decreasing no and proinflammatory cytokine production with less cytoxicity in LPS-stimulated raw 264.7 macrophages and LPS-induced septicemia mice. J Med Food 2014;17:1057-63. https://doi.org/10.1089/jmf.2013.3043
  18. Nencini C, Menchiari A, Franchi GG, Micheli L. In vitro antioxidant activity of aged extracts of some Italian Allium species. Plant Foods Hum Nutr 2011;66:11-6. https://doi.org/10.1007/s11130-010-0204-2
  19. Raschke WC, Baird S, Ralph P, Nakoinz I. Functional macrophage cell lines transformed by Abelson leukemia virus. Cell 1978;15:261-7. https://doi.org/10.1016/0092-8674(78)90101-0
  20. Birasuren B, Kim NY, Jeon HL, Kim MR. Evaluation of the antioxidant capacity and phenolic content of agriophyllum pungens seed extracts from Mongolia. Prev Nutr Food Sci 2013;18:188-95. https://doi.org/10.3746/pnf.2013.18.3.188
  21. Schwartz JN, Daniels CA, Shivers JC, Klintworth GK. Experimental cytomegalovirus ophthalmitis. Am J Pathol 1974;77:477-92.
  22. Fowler AJ, Sheu MY, Schmuth M, Kao J, Fluhr JW, Rhein L, Collins JL, Willson TM, Mangelsdorf DJ, Elias PM, Feingold KR. Liver X receptor activators display anti-inflammatory activity in irritant and allergic contact dermatitis models: liver-X-receptor-specific inhibition of inflammation and primary cytokine production. J Invest Dermatol 2003;120:246-55. https://doi.org/10.1046/j.1523-1747.2003.12033.x
  23. Jeon HL, Yoo JM, Lee BD, Lee SJ, Sohn EJ, Kim MR. Antiinflammatory and antioxidant actions of N-arachidonoyl serotonin in RAW264.7 cells. Pharmacology 2016;97:195-206. https://doi.org/10.1159/000443739
  24. Hamidzadeh K, Christensen SM, Dalby E, Chandrasekaran P, Mosser DM. Macrophages and the recovery from acute and chronic inflammation. Annu Rev Physiol 2017;79:567-92. https://doi.org/10.1146/annurev-physiol-022516-034348
  25. Upadhyay S, Dixit M. Role of polyphenols and other phytochemicals on molecular signaling. Oxid Med Cell Longev 2015;2015:504253.
  26. O'Neill LA. Toll-like receptor signal transduction and the tailoring of innate immunity: a role for Mal? Trends Immunol 2002;23:296-300. https://doi.org/10.1016/S1471-4906(02)02222-6
  27. Seo SH, Jeong GS. Fisetin inhibits $TNF-{\alpha}$-induced inflammatory action and hydrogen peroxide-induced oxidative damage in human keratinocyte HaCaT cells through PI3K/AKT/Nrf-2-mediated heme oxygenase-1 expression. Int Immunopharmacol 2015;29:246-53. https://doi.org/10.1016/j.intimp.2015.11.014
  28. Bito T, Nishigori C. Impact of reactive oxygen species on keratinocyte signaling pathways. J Dermatol Sci 2012;68:3-8. https://doi.org/10.1016/j.jdermsci.2012.06.006
  29. Park HJ, Jeon BT, Kim HC, Roh GS, Shin JH, Sung NJ, Han J, Kang D. Aged red garlic extract reduces lipopolysaccharide-induced nitric oxide production in RAW 264.7 macrophages and acute pulmonary inflammation through haeme oxygenase-1 induction. Acta Physiol (Oxf) 2012;205:61-70. https://doi.org/10.1111/j.1748-1716.2012.02425.x
  30. Nair AB, Jacob S. A simple practice guide for dose conversion between animals and human. J Basic Clin Pharm 2016;7:27-31. https://doi.org/10.4103/0976-0105.177703

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