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Microb Ecol Health Dis. 2015 May 06;26:26543. doi: 10.3402/mehd.v26.26543. eCollection 2015.

Composition, antimicrobial, antioxidant, and antiproliferative activity of Origanum dictamnus (dittany) essential oil.

Microbial ecology in health and disease

Gregoria Mitropoulou, Eleni Fitsiou, Elisavet Stavropoulou, Eleni Papavassilopoulou, Manolis Vamvakias, Aglaia Pappa, Antigoni Oreopoulou, Yiannis Kourkoutas

Affiliations

  1. Applied Microbiology and Molecular Biotechnology Research Group, Department of Molecular Biology & Genetics, Democritus University of Thrace, Alexandroupolis, Greece.
  2. Cellular and Molecular Physiology Research Group, Department of Molecular Biology & Genetics, Democritus University of Thrace, Alexandroupolis, Greece.
  3. Medical School, Democritus University of Thrace, Alexandroupolis, Greece.
  4. Vioryl, Chemical and Agricultural Industry, Research S.A., Afidnes, Greece.
  5. Applied Microbiology and Molecular Biotechnology Research Group, Department of Molecular Biology & Genetics, Democritus University of Thrace, Alexandroupolis, Greece; [email protected].

PMID: 25952773 PMCID: PMC4424236 DOI: 10.3402/mehd.v26.26543

Abstract

BACKGROUND: Nowadays, there has been an increased interest in essential oils from various plant origins as potential antimicrobial, antioxidant, and antiproliferative agents. This trend can be mainly attributed to the rising number and severity of food poisoning outbreaks worldwide along with the recent negative consumer perception against artificial food additives and the demand for novel functional foods with possible health benefits. Origanum dictamnus (dittany) is an aromatic, tender perennial plant that only grows wild on the mountainsides and gorges of the island of Crete in Greece.

OBJECTIVE: The aim of the present study was to investigate the antimicrobial, antioxidant, and antiproliferative properties of O. dictamnus essential oil and its main components and assess its commercial potential in the food industry.

DESIGN: O. dictamnus essential oil was initially analyzed by gas chromatography-mass spectrometry (GC-MS) to determine semi-quantitative chemical composition of the essential oils. Subsequently, the antimicrobial properties were assayed and the minimum inhibitory and non-inhibitory concentration values were determined. The antioxidant activity and cytotoxic action against the hepatoma adenocarcinoma cell line HepG2 of the essential oil and its main components were further evaluated by the 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay and by the sulforhodamine B (SRB) assay, respectively.

RESULTS: The main constituents of O. dictamnus essential oil identified by GC-MS analysis were carvacrol (52.2%), γ-terpinene (8.4%), p-cymene (6.1%), linalool (1.4%), and caryophyllene (1.3%). O. dictamnus essential oil and its main components were effective against Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Listeria monocytogenes, Salmonella Enteritidis, Salmonella typhimurium, Saccharomyces cerevisiae, and Aspergillus niger. In addition, the estimated IC50 value for the DPPH radical scavenging activity for O. dictamnus essential oil was 0.045±0.0042% (v/v) and was mainly attributed to carvacrol. The EC50 value for the essential oil in the 72h SRB assay in HepG2 cells was estimated to be 0.0069±0.00014% (v/v). Among the individual constituents tested, carvacrol was the most bioactive compound and accounted for the observed antiproliferative activity of the essential oil.

CONCLUSIONS: The results revealed that O. dictamnus essential oil is a noteworthy growth inhibitor against the microbes studied. It also possesses significant antioxidant activity and demonstrated excellent cytotoxicity against HepG2 cells. Taken together, O. dictamnus essential oil may represent an effective and inexpensive source of potent natural antimicrobial agents with health-promoting properties, which may be incorporated in food systems.

Keywords: GC–MS analysis; O. dictamnus essential oil; antimicrobial; antioxidant; antiproliferative

References

  1. Biomed Res Int. 2014;2014:154106 - PubMed
  2. Mol Cell Biochem. 2012 Jan;360(1-2):51-60 - PubMed
  3. Phytochemistry. 2006 Nov;67(22):2469-73 - PubMed
  4. Phytother Res. 2003 Feb;17(2):194-5 - PubMed
  5. Phytomedicine. 2010 Jul;17(8-9):581-8 - PubMed
  6. Food Microbiol. 2009 Dec;26(8):757-69 - PubMed
  7. J Appl Microbiol. 2003;95(4):734-43 - PubMed
  8. Int J Food Microbiol. 2013 Nov 1;167(3):310-21 - PubMed
  9. Neoplasma. 2014;61(6):690-9 - PubMed
  10. Free Radic Biol Med. 2007 Jun 1;42(11):1690-703 - PubMed
  11. J Sci Food Agric. 2013 Dec;93(15):3643-53 - PubMed
  12. J Appl Microbiol. 2001 Dec;91(6):1011-22 - PubMed
  13. Nat Prod Res. 2014;28(16):1284-7 - PubMed
  14. J Med Food. 2005 Summer;8(2):184-9 - PubMed
  15. J Appl Microbiol. 2006 Apr;100(4):778-86 - PubMed
  16. J Food Sci. 2012 Nov;77(11):C1156-61 - PubMed
  17. J Agric Food Chem. 2004 Dec 29;52(26):8261-7 - PubMed
  18. Int J Food Microbiol. 2004 Aug 1;94(3):223-53 - PubMed
  19. J Food Prot. 2013 Mar;76(3):538-51 - PubMed
  20. Life Sci. 2012 May 15;90(17-18):703-11 - PubMed
  21. Mutat Res. 2003 Feb-Mar;523-524:9-20 - PubMed
  22. J Nutr Biochem. 2013 Mar;24(3):586-94 - PubMed
  23. Appl Environ Microbiol. 2002 Apr;68(4):1901-6 - PubMed
  24. Nat Protoc. 2006;1(3):1112-6 - PubMed
  25. Food Chem Toxicol. 2014 Feb;64:281-90 - PubMed
  26. Fitoterapia. 2007 Jul;78(5):342-4 - PubMed
  27. Biochem Pharmacol. 2006 May 14;71(10):1397-421 - PubMed
  28. J Ethnopharmacol. 2010 Sep 15;131(2):229-41 - PubMed
  29. BMC Microbiol. 2005 Jun 17;5:36 - PubMed

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