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Anti-Inflammatory Effects of Odor Compounds

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Springer Handbook of Odor

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Abstract

Food-derived odor compounds determine the flavor of foods. However, these volatile compounds are known to elicit biological activities beyond their flavor function. Plants rich in volatile compounds, for example mint, have been used in traditional medicines worldwide to improve wound healing and to treat inflammation-related illnesses. In this chapter, we focus on the anti-inflammatory activity of different plant essential oils and individual odor compounds. Here, it is reviewed that odor compounds possess anti-inflammatory activity in pre- and postabsortive model systems, in vitro, ex vivo, and in vivo. Monocytes, macrophages, and fibroblasts are cells that play an important role in the innate immune response. In vitro models of these cells are commonly used to identify the mechanisms of action of the anti-inflammatory activity of volatile compounds. An inflammatory stimulus initiates the toll-like receptor-mediated signaling pathway, resulting in the gene expression and further the release of cytokines. Thus, an anti-inflammatory effect of odor compounds is measured by a reduction of cytokine messenger ribonucleic acid (GlossaryTerm

mRNA

) expression or release from stimulated cells. For example, eucalyptol, borneol, and camphor have been identified as anti-inflammatory active compounds that may be used to prevent or treat inflammation-related diseases.

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Abbreviations

ADI:

acceptable daily intake

CREB:

cAMP responsive element binding

DNA:

deoxyribonucleic acid

egr-1:

early growth response protein 1

GABA:

γ-amino butyric acid

GC:

gas chromatography

IFN-β:

interferon-β

IL:

interleukin

IκB:

inhibitory kappa B

LBP:

LPS-binding protein

LDL:

low density lipoprotein

LPS:

lipopolysaccharide

mRNA:

messenger ribonucleic acid

MSDI:

maximized survey-derived daily intake

MS:

mass spectrometry

mTAMDI:

modified theoretical added maximum daily intake

NF-κB:

nuclear factor kappa B

NOAEL:

no observed adverse effect level

PAMP:

pathogen-associated molecular pattern

PBMC:

peripheral blood mononuclear cell

RNA:

ribonucleic acid

TIR:

Toll/interleukin-1 receptor

TLR:

Toll-like receptor

TNF:

tumor necrosis factor

References

  1. G.B. Maru, L. Gandhi, A. Ramchandani, G. Kumar: The role of inflammation in skin cancer, Adv. Exp. Med. Biol. 816, 437–469 (2014)

    Article  CAS  Google Scholar 

  2. R. von Kanel, R.H. Carney, S. Zhao, M.A. Whooley: Heart rate variability and biomarkers of systemic inflammation in patients with stable coronary heart disease: Findings from the heart and soul study, Clin. Res. Cardiol. 100(3), 241–247 (2011)

    Article  Google Scholar 

  3. C.M. Volpe, L.F. Abreu, P.S. Gomes, R.M. Gouzaga, C.A. Veloso, J.A. Nogueira-Machado: The production of nitric oxide, IL-6, and TNF-alpha in palmitate-stimulated PBMNCs is enhanced through hyperglycemia in diabetes, Oxid. Med. Cell. Longev. 2014, 479–587 (2014)

    Article  Google Scholar 

  4. L.M. Bartoshuk: Comparing sensory experiences across individuals: Recent psychophysical advances illuminate genetic variation in taste perception, Chem. Senses 25(4), 447–460 (2000)

    Article  CAS  Google Scholar 

  5. W. Grosch: Detection of potent odorants in foods by aroma extract dilution analysis, Trends in Food Sci. Technol. 4(3), 68–73 (1993)

    Article  CAS  Google Scholar 

  6. T.E. Acree, J. Barnard, D.G. Cunningham: A procedure for the sensory analysis of gas-chromatographic effluents, Food Chem. 14(4), 273–286 (1984)

    Article  CAS  Google Scholar 

  7. J. Kiefl, C. Cordero, L. Nicolotti, P. Schieberle, S.E. Reichenbach, C. Bicchi: Performance evaluation of non-targeted peak-based cross-sample analysis for comprehensive two-dimensional gas chromatography-mass spectrometry data and application to processed hazelnut profiling, J. Chromatogr. A 1243, 81–90 (2012)

    Article  CAS  Google Scholar 

  8. A. Burdack-Freitag, P. Schieberle: Characterization of the key odorants in raw Italian hazelnuts (Corylus avellana L. var. Tonda Romana) and roasted hazelnut paste by means of molecular sensory science, J. Agri. Food Chem. 60(20), 5057–5064 (2012)

    Article  CAS  Google Scholar 

  9. P. Schieberle, D. Komarek: Changes in key aroma compounds during natural beer aging, Freshness and Shelf Life of Foods 836, 70–79 (2003)

    Article  CAS  Google Scholar 

  10. S. Frank, N. Wollmann, P. Schieberle, T. Hofmann: Reconstitution of the flavor signature of Dornfelder red wine on the basis of the natural concentrations of its key aroma and taste compounds, J. Agri. Food Chem. 59(16), 8866–8874 (2011)

    Article  CAS  Google Scholar 

  11. M. Averbeck, P.H. Schieberle: Characterisation of the key aroma compounds in a freshly reconstituted orange juice from concentrate, Eur. Food Res. Technol. 229(4), 611–622 (2009)

    Article  CAS  Google Scholar 

  12. J.S. Martin: Medicinal-plants in central Chile, Econ. Bot. 37(2), 216–227 (1983)

    Article  Google Scholar 

  13. D. van der Merwe, G.E. Swan, C.J. Botha: Use of ethnoveterinary medicinal plants in cattle by Setswana-speaking people in the Madikwe area of the North West Province of South Africa, J. S. Afr. Vet. Assoc.—Tydskri. Suid-Afrik. Vet. Ver. 72(4), 189–196 (2001)

    Google Scholar 

  14. C.L. Quave, A. Pieroni, B.C. Bennett: Dermatological remedies in the traditional pharmacopoeia of Vulture-Alto Bradano, inland Southern Italy, J. Ethnobiol. Ethnomed. 4, 5 (2008)

    Article  Google Scholar 

  15. A.L. Blasius, B. Beutler: Intracellular toll-like receptors, Immunity 32(3), 305–315 (2010)

    Article  CAS  Google Scholar 

  16. G.M. Barton, J.C. Kagan: A cell biological view of Toll-like receptor function: Regulation through compartmentalization, Nat. Rev. Immunol. 9(8), 535–542 (2009)

    Article  CAS  Google Scholar 

  17. K. Takeda, S. Akira: Toll-like receptors in innate immunity, Int. Immunol. 17(1), 1–14 (2005)

    Article  CAS  Google Scholar 

  18. T. Kawai, S. Akira: The role of pattern-recognition receptors in innate immunity: Update on toll-like receptors, Nat. Immunol. 11(5), 373–384 (2010)

    Article  CAS  Google Scholar 

  19. H. An, Y. Yu, M. Zhang, H. Xu, R. Qi, X. Yan, S. Liu, W. Wang, Z. Guo, J. Guo, Z. Qin, X. Cao: Involvement of ERK, p38 and NF-kappaB signal transduction in regulation of TLR2, TLR4 and TLR9 gene expression induced by lipopolysaccharide in mouse dendritic cells, Immunology 106(1), 38–45 (2002)

    Article  CAS  Google Scholar 

  20. O. Andrukhov, S. Ertlschweiger, A. Morit, H.P. Bantleon, X. Ranser-Fan: Different effects of P. gingivalis LPS and E. coli LPS on the expression of interleukin-6 in human gingival fibroblasts, Acta Odontol. Scand. 72(5), 337–345 (2013)

    Article  Google Scholar 

  21. K.H. Lim, L.M. Staudt: Toll-like receptor signaling, Cold Spring Harb. Perspect. Biol. 5(1), a011247 (2013)

    Article  Google Scholar 

  22. M.J. Berridge: Cell Signalling Biology, www.cellsignallingbiology.org (2014), doi:10.1042csb0001002

  23. A.S. Dhillon, S. Hagan, O. Rath, W. Kolch: MAP kinase signalling pathways in cancer, Oncogene 26(22), 3279–3290 (2007)

    Article  CAS  Google Scholar 

  24. T. Zarubin, J.H. Han: Activation and signaling of the p38 MAP kinase pathway, Cell Res. 15(1), 11–18 (2005)

    Article  CAS  Google Scholar 

  25. P. Kalinski: Regulation of immune responses by prostaglandin E2, J. Immunol. 188(1), 21–28 (2012)

    Article  CAS  Google Scholar 

  26. T. Glaros, M. Larsen, L.W. Li: Macrophages and fibroblasts during inflammation, tissue damage and organ injury, Front. Biosci. 14, 3988–3993 (2009)

    Article  CAS  Google Scholar 

  27. B. Eksteen, L.S. Walker, D.H. Adams: Immune regulation and colitis: Suppression of acute inflammation allows the development of chronic inflammatory bowel disease, Gut 54(1), 4–6 (2005)

    Article  CAS  Google Scholar 

  28. T. Polte, L. Fuchs, A.K. Behrendt, G. Hanser: Different role of CD30 in the development of acute and chronic airway inflammation in a murine asthma model, Eur. J. Immunol. 39(7), 1736–1742 (2009)

    Article  CAS  Google Scholar 

  29. R. Mahanonda, N. Sa-ard-lam, P. Montreekachon, E.A. Pimkhaokam, K. Yongvanichit, M.M. Fukada, S. Pichyangkul: IL-8 and IDO expression by human gingival fibroblasts via TLRs, J. Immunol. 178(2), 1151–1157 (2007)

    Article  CAS  Google Scholar 

  30. J.M. Walker, A. Maitra, J. Walker, M.M. Ehrnhoefer-Ressler, T. Inui, V. Somoza: Identification of Magnolia officinalis L. bark extract as the most potent anti-inflammatory of four plant extracts, Am. J. Chin. Med. 41(3), 531–544 (2013)

    Article  Google Scholar 

  31. C. Bodet, F. Chandad, D. Grenier: Cranberry components inhibit interleukin-6, interleukin-8, and prostaglandin E production by lipopolysaccharide-activated gingival fibroblasts, Eur. J. Oral Sci. 115(1), 64–70 (2007)

    Article  CAS  Google Scholar 

  32. L. Zhao, V.D. La, D. Grenier: Antibacterial, antiadherence, antiprotease, and anti-inflammatory activities of various tea extracts: Potential benefits for periodontal diseases, J. Med. Food 16(5), 428–436 (2013)

    Article  Google Scholar 

  33. J.Y. Hong, S.H. Lee, T.H. Kim, J. Hong, K.M. Lee, S.D. Yoo, H.S. Lee: GC-MS/MS method for the quantification of alpha-cedrene in rat plasma and its pharmacokinetic application, J. Sep. Sci. 36(21-22), 3558–3562 (2013)

    Article  CAS  Google Scholar 

  34. H.H. Chow, D. Salazar, I.A. Hakim: Pharmacokinetics of perillic acid in humans after a single dose administration of a citrus preparation rich in d-limonene content, Cancer Epidemiol. Biomark. Prev. 11(11), 1472–1476 (2002)

    CAS  Google Scholar 

  35. W. Chanput, J. Mes, R.A. Vreeburg, H.F. Savelkoul, H.J. Wichers: Transcription profiles of LPS-stimulated THP-1 monocytes and macrophages: A tool to study inflammation modulating effects of food-derived compounds, Food Funct. 1(3), 254–261 (2010)

    Article  CAS  Google Scholar 

  36. J. Walker, K. Schueller, L.M. Schaefer, M. Pignitter, L. Esefelder, V. Somoza: Resveratrol and its metabolites inhibit pro-inflammatory effects of lipopolysaccharides in U-937 macrophages in plasma-representative concentrations, Food Funct. 5(1), 74–84 (2014)

    Article  CAS  Google Scholar 

  37. E. Jones, I.M. Adcock, B.Y. Ahmed, N.A. Punchard: Modulation of LPS stimulated NF-kappaB mediated Nitric Oxide production by PKCepsilon and JAK2 in RAW macrophages, J. Inflamm. 4, 23 (2007), London

    Article  Google Scholar 

  38. E. Keinan, A. Alt, G. Amir, L. Bentur, H. Bibi, D. Shoseyov: Natural ozone scavenger prevents asthma in sensitized rats, Bioorg. Med. Chem. 13(2), 557–562 (2005)

    Article  CAS  Google Scholar 

  39. F. Lara-Villoslada, O. de Haro, D. Camuesco, M. Comalada, J. Velasco, A. Zarzuelo, J. Xaus, J. Galvez: Short-chain fructooligosaccharides, in spite of being fermented in the upper part of the large intestine, have anti-inflammatory activity in the TNBS model of colitis, Eur. J. Nutr. 45(7), 418–425 (2006)

    Article  CAS  Google Scholar 

  40. I. Tumen, I. Süntar, F.J. Eller, H. Kelezz, E.K. Aikkol: Topical wound-healing effects and phytochemical composition of heartwood essential oils of Juniperus virginiana L., Juniperus occidentalis Hook., and Juniperus ashei J. Buchholz, J. Med. Food 16(1), 48–55 (2013)

    Article  CAS  Google Scholar 

  41. I. Peluso, A. Raguzzini, M. Serafini: Effect of flavonoids on circulating levels of TNF-alpha and IL-6 in humans: A systematic review and meta-analysis, Mol. Nutr. Food Res. 57(5), 784–801 (2013)

    Article  CAS  Google Scholar 

  42. M.R. Ritchie, J. Gertsch, P. Klein, R. Schoop: Effects of Echinaforce (R) treatment on ex vivo-stimulated blood cells, Phytomedicine 18(10), 826–831 (2011)

    Article  CAS  Google Scholar 

  43. A. Sfakianakis, C.E. Barr, D.L. Kreutzer: Actinobacillus actinomycetemcomitans-induced expression of IL-1alpha and IL-1beta in human gingival epithelial cells: Role in IL-8 expression, Eur. J. Oral Sci. 109(6), 393–401 (2001)

    Article  CAS  Google Scholar 

  44. R. Spooner, J. DeGuzman, K.L. Lee, O. Yilmaz: Danger signal adenosine via adenosine 2a receptor stimulates growth of Porphyromonas gingivalis in primary gingival epithelial cells, Mol. Oral Microbiol. 29(2), 67–78 (2014)

    Article  CAS  Google Scholar 

  45. S. Held, P. Schieberle, V. Somoza: Characterization of alpha-terpineol as an anti-inflammatory component of orange juice by in vitro studies using oral buccal cells, J. Agric. Food Chem. 55(20), 8040–8046 (2007)

    Article  CAS  Google Scholar 

  46. M.M. Ehrnhofer-Ressler, K. Fricke, M. Pignitter, J.M. Walker, J. Walker, M. Rychlik, V. Somoza: Identification of 1,8-cineole, borneol, camphor, and thujone as anti-inflammatory compounds in a Salvia officinalis L. infusion using human gingival fibroblasts, J. Agric. Food Chem. 61(14), 3451–3459 (2013)

    Article  Google Scholar 

  47. F.A. Santos, R.M. Silva, A.R. Campos, R.P. De Araújo, R.C. Lima Júnior, V.S. Rao: 1,8-cineole (eucalyptol), a monoterpene oxide attenuates the colonic damage in rats on acute TNBS-colitis, Food Chem. Toxicol. 42(4), 579–584 (2004)

    Article  CAS  Google Scholar 

  48. C. Zhao, J. Sun, C. Fang, T. Tang: 1,8-cineol attenuates LPS-induced acute pulmonary inflammation in mice, Inflammation 37(2), 566–572 (2014)

    Article  CAS  Google Scholar 

  49. H. Worth, U. Dethlefsen: Patients with asthma benefit from concomitant therapy with cineole: A placebo-controlled, double-blind trial, J. Asthma 49(8), 849–853 (2012)

    Article  CAS  Google Scholar 

  50. U.R. Juergens, U. Dethlefsen, G. Steinkamp, A. Gillissen, R. Repges, H. Ve Her: Anti-inflammatory activity of 1.8-cineol (eucalyptol) in bronchial asthma: A double-blind placebo-controlled trial, Respir. Med. 97(3), 250–256 (2003)

    Article  CAS  Google Scholar 

  51. V. Woguem, H.P. Fogang, F. Maggi, L.A. Tapondjou, H.M. Womwni, L. Quassiuti, M. Bramucci, L.A. Vitali, D. Petrelli, G. Lupidi, F. Papa, S. Vittori, L. Barboui: Volatile oil from striped African pepper (Xylopia parviflora, Annonaceae) possesses notable chemopreventive, anti-inflammatory and antimicrobial potential, Food Chem. 149, 183–189 (2014)

    Article  CAS  Google Scholar 

  52. Y.T. Tung, M.T. Chua, S.Y. Wang, S.T. Chang: Anti-inflammation activities of essential oil and its constituents from indigenous cinnamon (Cinnamomum osmophloeum) twigs, Bioresour. Technol. 99(9), 3908–3913 (2008)

    Article  CAS  Google Scholar 

  53. W.J. Yoon, J.Y. Moon, G. Song, Y.K. Lee, M.S. Han, J.S. Lee, B.S. Ihm, W.J. Lee, N.H. Lee, C.G. Hyun: Artemisia fukudo essential oil attenuates LPS-induced inflammation by suppressing NF-kappaB and MAPK activation in RAW 264.7 macrophages, Food Chem. Toxicol. 48(5), 1222–1229 (2010)

    Article  CAS  Google Scholar 

  54. M.L. Tsai, C.C. Lin, W.C. Lin, C.H. Yang: Antimicrobial, antioxidant, and anti-inflammatory activities of essential oils from five selected herbs, Biosci. Biotechnol. Biochem. 75(10), 1977–1983 (2011)

    Article  CAS  Google Scholar 

  55. I. Takaki, L.E. Bersni-Amado, A. Vendruscolo, S.M. Sartoretto, S.P. Diniz, C.A. Bersani-Amado, R.K. Cuman: Anti-inflammatory and antinociceptive effects of Rosmarinus officinalis L. essential oil in experimental animal models, J. Med. Food 11(4), 741–746 (2008)

    Article  CAS  Google Scholar 

  56. G.A. Nogueira de Melo, R. Grespn, J.P. Fonseca, T.O. Fariuha, E.L. Silv, A.L. Romero, C.A. Bersani-Amado, R.K. Cuman: Rosmarinus officinalis L. essential oil inhibits in vivo and in vitro leukocyte migration, J. Med. Food 14(9), 944–946 (2011)

    Article  CAS  Google Scholar 

  57. A. Ocana-Fuentes, E. Arrauz-Guitiérrez, F.J. Señoraus, G. Reglero: Supercritical fluid extraction of oregano (Origanum vulgare) essentials oils: Anti-inflammatory properties based on cytokine response on THP-1 macrophages, Food Chem. Toxicol. 48(6), 1568–1575 (2010)

    Article  CAS  Google Scholar 

  58. J.Y. Zhou, X.F. Wang, F.D. Tang, J.Y. Zhou, G.H. Lu, Y. Wang, R.L. Bian: Inhibitory effect of 1,8-cineol (eucalyptol) on Egr-1 expression in lipopolysaccharide-stimulated THP-1 cells, Acta Pharmacol. Sin. 28(6), 908–912 (2007)

    Article  CAS  Google Scholar 

  59. U.R. Juergens, T. Engelen, K. Racké, M. Stöber, A. Gillissen, H. Vetter: Inhibitory activity of 1,8-cineol (eucalyptol) on cytokine production in cultured human lymphocytes and monocytes, Pulm. Pharmacol. Ther. 17(5), 281–287 (2004)

    Article  CAS  Google Scholar 

  60. R. de Cassia da Silveira e Sa, L.N. Andrade, D.P. de Sousa: A review on anti-inflammatory activity of monoterpenes, Molecules 18(1), 1227–1254 (2013)

    Google Scholar 

  61. D. Martin, J. Valdez, J. Boren, M. Mayersohn: Dermal absorption of camphor, menthol, and methyl salicylate in humans, J. Clin. Pharmacol. 44(10), 1151–1157 (2004)

    Article  CAS  Google Scholar 

  62. D.W. Lachenmeier, S.G. Walch, S.A. Padosch, L.U. Kröner: Absinthe – A review, Crit. Rev. Food Sci. Nutr. 46(5), 365–377 (2006)

    Article  CAS  Google Scholar 

  63. O. Pelkonen, K. Abass, J. Wiesner: Thujone and thujone-containing herbal medicinal and botanical products: Toxicological assessment, Regul. Toxicol. Pharmacol. 65(1), 100–107 (2013)

    Article  CAS  Google Scholar 

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Walker, J., Somoza, V. (2017). Anti-Inflammatory Effects of Odor Compounds. In: Buettner, A. (eds) Springer Handbook of Odor. Springer Handbooks. Springer, Cham. https://doi.org/10.1007/978-3-319-26932-0_35

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